<?xml version="1.0" encoding="utf-8"?><rss version="2.0" xmlns:dataField="https://www.inteum.com/technologies/data/"><channel><title>Latest technologies from Canberra IP</title><link>https://canberra-ip.technologypublisher.com</link><description>Be the first to know about the latest inventions and technologies available from Canberra IP</description><language>en-US</language><pubDate>Thu, 16 Apr 2026 08:36:13 GMT</pubDate><lastBuildDate>Thu, 16 Apr 2026 08:36:13 GMT</lastBuildDate><docs>https://cyber.harvard.edu/rss/rss.html</docs><webMaster>support@inteum.com</webMaster><copyright>Copyright 2026, Canberra IP</copyright><item><title>Polymers of Intrinsic Microporosity for Improved Smart Device and Display Technologies</title><link>https://canberra-ip.technologypublisher.com/tech/Polymers_of_Intrinsic_Microporosity_for_Improved_Smart_Device_and_Display_Technologies</link><description><![CDATA[<h3><em>Electrochromic Devices Rapidly Changing Color for Supercapacitive and Pseudocapacitive Energy Storage</em></h3>

<p>These polymers of intrinsic microporosity (PIMs) use electrochromic materials that change color in response to an applied voltage for improved energy storage. Electrochromic materials switch color when a voltage potential is applied. These materials are widely used in smart windows, displays, and advanced optics due to their electrochemical stability, moderate operating voltages, and high optical contrasts. However, existing electrochromic materials are constrained by slow switching speeds, limiting their effectiveness in next-generation devices and applications.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida have developed electrochromic materials that improve switching speeds while maintaining the key benefits of current materials. These materials are solution-processable PIMs, which are straightforward to manufacture and can be fabricated into thin films without the use of toxic solvents or transition metals. This technology represents a substantial improvement over current electrochromic systems and enables faster, safer, more energy-efficient display, window, and optic technologies.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>Fast-switching PIMs enable high-performance, energy-efficient electrochromic devices for smart windows, displays and advanced optics</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Materials do not require conductive additive or stabilizing binder, significantly lowering the cost of manufacturing</li>
	<li>Scalable fabrication for large-area devices, accelerating production timeline</li>
	<li>Ability to be manufactured without toxic solvents, increasing safety of material</li>
	<li>Switching speeds of around one second represents a drastic advantage over other electrochromic materials in use today</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>This technology uses viologen-based polymers of intrinsic microporosity (PIMs) engineered for rapid electrochromic switching in solid-state devices. The PIMs are synthesized using contorted spirobisindane building blocks to create permanent nanoporous channels throughout the polymer matrix. These channels facilitate efficient ion transport and reduce charge transfer resistance, enabling swift and reversible color changes across the visible spectrum when a reductive bias is applied. The solution-processable nature of these PIMs allows for uniform thin-film deposition onto conductive substrates, forming two-terminal electrochromic devices with gel electrolytes. The materials demonstrate high optical contrast, elevated coloration efficiency, and robust cycling stability, all achieved without toxic solvents or transition metals. This combination of rapid switching, processability, and performance positions PIMs as a platform for next-generation mixed ionic-electronic conducting applications.</p>]]></description><pubDate>Thu, 16 Apr 2026 08:32:13 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Polymers_of_Intrinsic_Microporosity_for_Improved_Smart_Device_and_Display_Technologies</guid><dataField:caseId>MP25097</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 08:32:13 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Austin</dataField:firstName><dataField:lastName>Evans</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>austinevans@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Mahmudul</dataField:firstName><dataField:lastName>Hasan</dataField:lastName><dataField:title></dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>ammahmudulhasan@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Rupam</dataField:firstName><dataField:lastName>Roy</dataField:lastName><dataField:title></dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>rupam.roy@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Kiana</dataField:firstName><dataField:lastName>Treaster</dataField:lastName><dataField:title></dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>treaster.kiana@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Kaitlin</dataField:firstName><dataField:lastName>Slicker</dataField:lastName><dataField:title></dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>k.slicker@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Ani</dataField:firstName><dataField:lastName>Davis</dataField:lastName><dataField:title></dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>ani.davis@chem.ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Dibakar</dataField:firstName><dataField:lastName>Das</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>ddas@sinmat.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Chemical| Technology Classifications > Engineering > Materials]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Smart Onsite Black Water Purification System for Water and Nutrient Recycling</title><link>https://canberra-ip.technologypublisher.com/tech/Smart_Onsite_Black_Water_Purification_System_for_Water_and_Nutrient_Recycling</link><description><![CDATA[<h3><em>Reuses Wastewater, Enabling the Near-Perpetual Reuse of the Same Volume of Water</em></h3>

<p>This blackwater purification system reuses wastewater to enable the near-perpetual reuse of the same water volume, generating reusable wastewater. Worldwide, sanitation systems primarily rely on centralized wastewater and sewage treatment plants, with onsite septic systems used in certain developed regions. While blackwater purification technologies offer the potential for near-continuous reuse of water by treating wastewater for repeated cycles, existing centralized systems require significant capital investment and high energy inputs to operate. Moreover, system failures can lead to the release of microbe-, chemical-, and nutrient-laden effluent, contaminating ground and surface waters, accelerating eutrophication, and posing serious public health risks to surrounding communities.</p>

<p>&nbsp;</p>

<p>Regulatory standards require wastewater to meet defined treatment thresholds before it is discharged into surface water bodies. In many conventional systems, the absence of source separation results in the combination of greywater, blackwater, and stormwater into a single flow. During periods of heavy use or intense rainfall, treatment plants can exceed their design capacity, resulting in bypass events where untreated wastewater and raw sewage are released directly into rivers, lakes, or coastal waters. These discharges introduce harmful microorganisms, nutrients, and chemicals into the environment, posing significant risks to both ecosystems and public health. Decentralized residential wastewater systems, such as septic tanks, are not immune to these issues; when poorly maintained or overloaded, they can similarly contaminate groundwater and contribute to waterborne disease outbreaks. Despite these critical challenges, there is a clear and pressing gap in the market: the absence of smart, environmentally friendly, and compact onsite blackwater purification systems. Addressing this gap is essential to advancing sustainable water management, particularly in resource-limited or decentralized settings.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida have developed a decentralized, compact, and cost-effective blackwater purification system designed for on-site use. This system enables the near-continuous reuse of the same volume of water by integrating multiple advanced treatment technologies, ensuring it meets or exceeds established standards for toilet water reuse. As a byproduct, the process generates biochar, which can be applied to agricultural land as a soil amendment&mdash;delivering significant environmental and agricultural benefits. The adaptable and energy-efficient purification system reduces the environmental impact, lowers operational costs, and safeguards public health, while enabling communities to reuse water in a near-perpetual cycle.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>Smart, decentralized, and compact onsite sanitation system, enabling the reuse of wastewater and application of biochar to agricultural land</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Intelligent, sustainable sanitation, brings smart technology to decentralized wastewater management</li>
	<li>Compact and portable design engineered for flexibility, making it easy to deploy anywhere, from remote communities to urban developments</li>
	<li>Cost-effective solution, delivering reliable sanitation at a fraction of the cost of large, centralized treatment facilities</li>
	<li>Water reuse capability integrates multiple advanced treatment technologies to enable the perpetual, on-site reuse of the same volume of water, dramatically reducing freshwater demand</li>
	<li>Environment-enhancing byproducts produce biochar as a valuable end product, enriching agricultural soils, boosting crop growth, and supporting carbon sequestration for a healthier planet</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>This eco-friendly sanitation technology transforms blackwater into a safe, reusable resource, cutting waste and dramatically lowering toilet system costs. Blackwater is pumped through a grinder into an advanced aboveground vessel, where thermophilic and aerobic digestion sterilize the mixture using naturally generated heat. The slurry then flows through a biochar filtration module that captures nutrients and eliminates harmful bacteria. The result is clean, safe water that can be recirculated to the toilet&mdash;enabling near-perpetual reuse of the same water volume. This closed-loop process delivers unmatched sustainability, operational efficiency, and long-term savings, making it a game-changing solution for modern sanitation and water management.</p>]]></description><pubDate>Thu, 16 Apr 2026 08:14:51 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Smart_Onsite_Black_Water_Purification_System_for_Water_and_Nutrient_Recycling</guid><dataField:caseId>MP25031</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 08:18:40 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Nawari</dataField:firstName><dataField:lastName>Nawari</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>DCP-SCHOOL OF ARCHITECTURE</dataField:department><dataField:emailAddress>nnawari@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Heidemarie</dataField:firstName><dataField:lastName>Wittmann</dataField:lastName><dataField:title>Alumni</dataField:title><dataField:department>SA-REGISTRAR STUDENT</dataField:department><dataField:emailAddress>heidiw524@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Volk</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>DCP-LANDSCAPE ARCHITECTURE</dataField:department><dataField:emailAddress>mikevolk@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Mechanical| Technology Classifications > Others > Cleantech]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Methods To Regulate Metabolism For Treatment Of Neural Injuries and Neurodegeneration</title><link>https://canberra-ip.technologypublisher.com/tech/Methods_To_Regulate_Metabolism_For_Treatment_Of_Neural_Injuries_and_Neurodegeneration</link><description><![CDATA[<p>Axonal injury and subsequent neuronal death underpin the pathology of many neurological disorders from acute neural injuries (motor vehicle crashes, combat related injuries, traumatic brain injuries) to neurological diseases (multiple sclerosis, glaucoma). In the central nervous system (CNS), microglia help respond to CNS injuries by mediating the immune response and increasing inflammation at the site of injury.&nbsp;</p>

<p>Scientists at the National Eye Institute (NEI) have discovered a novel method of reducing neuronal death by using Dimethyl Malonate (DMM), a compound that inhibits the activity of succinate dehydrogenase (SDH). Using DMM on an optic nerve crush model in ground squirrels, DMM helped reduce the pro-inflammatory response of microglia via decreasing succinate levels or reducing the SDH activity. In the same model, treatment also improved the retinal function compared to controls. Additionally, administering DMM after optic crush injury reduced the microglia response and promoted neural protection against axonal injury.&nbsp;</p>

<p>This method of treats immune-mediated disorders using DMM by decreasing levels of succinate or reducing the activity of succinate dehydrogenase in patients. It inhibits activation of microglial cells by using DMM by decreasing levels of succinate or reducing the activity of succinate dehydrogenase in cells. It prevents the activation of astrocytes in a system comprising of microglial cells and astrocytes using DMM by decreasing levels of succinate or reducing the activity of succinate dehydrogenase. Overall, these results show the promise of DMM for protecting neurodegeneration due to neural injury and possibly other neurodegenerative disorders.</p>

<h2>Potential Commercial Applications:&nbsp;</h2>

<p>&bull; Ophthalmic diseases, such as glaucoma<br />
&bull; Neurodegenative diseases, such as multiple sclerosis<br />
&bull; Acute neural injuries</p>

<h2><strong>Competitive Advantages:&nbsp;</strong></h2>

<p>&bull; Dimethyl Malonate (DMM) is inexpensive and readily available &ndash; reducing manufacturing costs<br />
&bull; Address significant, unmet medical needs since few, if any, treatments exist for neural injuries and neurodegeneration<br />
&bull; Mutation independent method for treating neurodegeneration<br />
&nbsp;</p>]]></description><pubDate>Thu, 16 Apr 2026 07:15:08 GMT</pubDate><author>nihott@nih.gov</author><guid>https://canberra-ip.technologypublisher.com/tech/Methods_To_Regulate_Metabolism_For_Treatment_Of_Neural_Injuries_and_Neurodegeneration</guid><dataField:caseId>TAB-4999</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 07:15:08 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Wei</dataField:firstName><dataField:lastName>Li</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Jingxing</dataField:firstName><dataField:lastName>Ou</dataField:lastName><dataField:title>Visiting Fellow</dataField:title><dataField:department></dataField:department><dataField:emailAddress>ouj@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>301-402-7685</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Tantai</dataField:firstName><dataField:lastName>Zhao</dataField:lastName><dataField:title>Visiting Fellow</dataField:title><dataField:department></dataField:department><dataField:emailAddress>tantai.zhao@nih.gov</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Ricquita</dataField:firstName><dataField:lastName>Pollard</dataField:lastName><dataField:title>Technology Transfer Manager</dataField:title><dataField:department>TTC</dataField:department><dataField:emailAddress>ricquita.pollard@nih.gov</dataField:emailAddress><dataField:phoneNumber>240-276-5530</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Application > Therapeutics| Collaboration Sought > Collaboration| TherapeuticArea > Ear, Nose, & Throat| TherapeuticArea > Neurology| Collaboration Sought > Licensing]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Ultra-Smooth Single-Crystal Diamond Surfaces for Enhanced Device Performance</title><link>https://canberra-ip.technologypublisher.com/tech/Ultra-Smooth_Single-Crystal_Diamond_Surfaces_for_Enhanced_Device_Performance</link><description><![CDATA[<h3><em>Reduces Surface Roughness and Spike Density Through Extended UV-Ozone Exposure</em></h3>

<p>This diamond smoothing method via extended UV-ozone exposure enhances device performance and reliability by reducing surface roughness and spike density. Diamond-based devices, such as rectifiers, offer significant potential for high-power and high-frequency applications. These devices possess exceptional properties, including high breakdown voltage, low leakage current, and high thermal conductivity. However, production is hindered by current surface smoothing technologies&rsquo; limitations. Existing methods often rely on material removal through etching, which result in an uneven surface, forming etch pits. These damages to the device surface cause increased leakage currents, reduced breakdown voltages, and degraded electronic and thermal properties, ultimately reducing the device&rsquo;s reliability and performance. To overcome the challenges and unlock the full potential of diamond-based devices, there is an evident need for a non-invasive, reliable technique to achieve ultra-smooth diamond surfaces.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida have developed a diamond smoothing method via extended UV-ozone exposure that enhances device performance and reliability by reducing surface roughness and spike density. It enables the production of ultra-smooth, high-quality diamond devices with improved breakdown voltages, reduced leakage currents, and enhanced thermal conductivity. By providing a non-invasive way to smoothen diamond surfaces, this method offers a competitive advantage in the development of high-power electronic devices and holds great potential to revolutionize industries such as power electronics.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>&nbsp;</p>

<p>UV-ozone smoothing method supports manufacturing ultra-smooth diamond surfaces for high-power and high-frequency electronic devices</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Improves surface roughness, enabling high-quality diamond-based rectifiers</li>
	<li>Increases breakdown voltage by 30% through 60 minutes of exposure, enhancing device performance and reducing failure rates</li>
	<li>Preserves diamond lattice integrity, minimizing defects and maintaining material properties</li>
	<li>Boosts nitrogen-vacancy (NV) center quality, paving the way for greater potential for quantum sensing, information processing, and communication applications</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>This diamond smoothing technology via extended UV-ozone exposure enhances device performance and reliability by reducing surface roughness and spike density. Extended UV-ozone exposure progressively oxidizes surface irregularities, eliminating high-aspect-ratio spikes and reducing root-mean-square (RMS) surface roughness. Additionally, this method avoids creating new defects or damaging the diamond surface. The reaction of ozone with surface contaminants results in a smooth and defect-free surface.</p>]]></description><pubDate>Thu, 16 Apr 2026 06:17:07 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Ultra-Smooth_Single-Crystal_Diamond_Surfaces_for_Enhanced_Device_Performance</guid><dataField:caseId>MP25096</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 06:21:45 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Fan</dataField:firstName><dataField:lastName>Ren</dataField:lastName><dataField:title>Professor</dataField:title><dataField:department>EG-CHEMICAL ENGINEERING</dataField:department><dataField:emailAddress>fren@che.ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Chao-Ching</dataField:firstName><dataField:lastName>Chiang</dataField:lastName><dataField:title>Employee</dataField:title><dataField:department>EG-CHEMICAL ENGINEERING</dataField:department><dataField:emailAddress>cchiang@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Stephen</dataField:firstName><dataField:lastName>Pearton</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>EG-MATERIALS SCI ENGINEERING</dataField:department><dataField:emailAddress>spear@mse.ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Chemical| Technology Classifications > Engineering > Electrical| Technology Classifications > Engineering| Technology Classifications > Engineering > Materials]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Thermal Depolymerization Etching of Microphase Separations for Creating High-Surface-Area Polymers</title><link>https://canberra-ip.technologypublisher.com/tech/Thermal_Depolymerization_Etching_of_Microphase_Separations_for_Creating_High-Surface-Area_Polymers</link><description><![CDATA[<h3><em>Enables Rapid, Solvent-Free Formation of Mesoporous Materials by Selectively Removing Methacrylate Domains</em></h3>

<p>Thermal depolymerization etching enables rapid, solvent-free formation of high-surface-area mesoporous polymers by selectively removing methacrylate domains. Etching approaches are used to generate nanoscale porosity in polymers. However, existing methods rely on solution-based processes that suffer from slow transport of etching agents and the degradation products arising from pore formation. These constraints become more significant in bulk materials, where transport limitations reduce efficiency and make it difficult to obtain uniform porous structures. Meanwhile, demand for advanced filtration and separation technologies continues to grow, with the global filtration and separation market estimated at approximately $184.75 USD billion in 2024 and projected to exceed $276 USD billion by 2035, reflecting the increasing need for high-performance materials in this space . Therefore, there is a clear need for fast, scalable etching methods that can reliably produce well-defined mesoporous polymers at commercial volumes.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida have discovered depolymerization etching of polymerization-induced microphase separations (DEPIMS), a rapid, solvent-free thermal process that enables efficient formation of porous polymer systems. This approach selectively removes polymethacrylate domains while maintaining the overall polystyrene structure, allowing scalable, on-demand fabrication of well-defined, high-surface-area mesoporous materials.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>Produces high-surface-area mesoporous polymer materials for separations, adsorption, and purification applications</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Enables rapid, solvent-free mesoporous polymer formation, cutting processing time</li>
	<li>Delivers high surface area, boosting catalyst loading or adsorption capacity</li>
	<li>Supports one-pot bulk synthesis, allowing gram-scale, streamlined production</li>
	<li>Selectively removes specific polymer domains, maintaining structural matrix integrity</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>This etching approach is based on a process called DEPIMS &ndash; depolymerization etching of polymerization-induced microphase separation. First, a polymer system is formed through the incorporation of a depolymerizable component into a crosslinked matrix that resists degradation. During formation, the material undergoes simultaneous growth, phase separation, and crosslinking, producing a continuous structure with nanoscale domains. Heating the material to elevated temperatures causes the depolymerizable regions to break down into monomer species that are removed, while the crosslinked framework remains intact. This selective removal process results in a porous material with interconnected nanoscale features that can be further functionalized with chemical moeties promoting selective filtration, adsorption, etc. Because the removed components exit as rapidly diffusing species, the process bypasses the transport limitations associated with liquid-based etching and enables efficient formation of high-surface-area materials.</p>]]></description><pubDate>Thu, 16 Apr 2026 05:48:29 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Thermal_Depolymerization_Etching_of_Microphase_Separations_for_Creating_High-Surface-Area_Polymers</guid><dataField:caseId>MP26037</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 06:00:42 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Brent</dataField:firstName><dataField:lastName>Sumerlin</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>LS-CHEMISTRY</dataField:department><dataField:emailAddress>sumerlin@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Kaden</dataField:firstName><dataField:lastName>Stevens</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>kadenstevens@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>James</dataField:firstName><dataField:lastName>Young</dataField:lastName><dataField:title>Employee</dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>jyoung@tritonsys.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Jared</dataField:firstName><dataField:lastName>Bowman</dataField:lastName><dataField:title>Employee</dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>jared.bowman@usm.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Megan</dataField:firstName><dataField:lastName>Lott</dataField:lastName><dataField:title>GRADUATE AST</dataField:title><dataField:department>LS-CHEMISTRY</dataField:department><dataField:emailAddress>m.lott@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Cabell</dataField:firstName><dataField:lastName>Eades</dataField:lastName><dataField:title>Graduate Student</dataField:title><dataField:department>LS-CHEMISTRY-GENERAL</dataField:department><dataField:emailAddress>ceades@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Chemical| Technology Classifications > Engineering > Electrical| Technology Classifications > Engineering > Materials| Technology Classifications > Others > Cleantech]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>OPTICALLY ENCODED DNA BARCODE PARTICLES</title><link>https://canberra-ip.technologypublisher.com/tech/OPTICALLY_ENCODED_DNA_BARCODE_PARTICLES</link><description><![CDATA[<p>Researchers at Stanford have developed a novel method for the barcoding of DNA.</p>

<p>Over the past decade, single-cell sequencing has become widely used in biology and medicine. To analyze many cells at once, each cell must be labeled with a unique DNA barcode so its molecules can be identified after sequencing. This is usually done by capturing cells on barcode beads, where each bead carries a different DNA sequence. However, because these barcodes are randomly generated and randomly paired with cells, researchers cannot know which barcode belongs to which cell before sequencing, making it difficult to link sequencing data with other measurements from the same cell. This creates a clear gap in the market for barcoding approaches that provide predefined, traceable cell identities prior to sequencing.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention, Optically Recognizable Barcoded Beads (ORBBs), comprises a method in which each barcode bead is optically unique such that the DNA sequence for a given bead can be determined by imaging the bead with a fluorescent microscope. The key idea behind ORBBs is that each bead has geometrically distinct regions that can be fluorescently labeled within a single bead. This drastically increases the number of unique fluorescent barcodes that can be produced by these beads. ORBBs are able to be barcoded through the same standard split pool process that other commercially available barcoded beads use with one key modification - each well the barcode beads pass through has a unique combination of oligo conjugated fluorophores, creating a unique barcode on each bead. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li ><strong>Imaging-based cellular experiments: </strong>ORBBs are able to be used technological platforms that enable imaging based cellular measurements to be linked to sequencing based measurements, allowing researchers to investigate how genotype and gene expression influence cellular phenotype. </li>
	<li ><strong>Spatial Transcriptomics: </strong>The use of ORBBs would allow researchers to do single-cell (or small-number of cell) sequencing on tissues while preserving the location of the cell with respect to the rest of the tissue. </li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li ><strong>Throughput and Usability: </strong>A commercialized ORBBs product could be paired with microwell sequencing assays, giving any biology lab the ability to run imaging and sequencing based multi-omic assays.</li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Barcode, Optical</p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-326B</p>

<p>UC Berkeley re. no. BK2025-075</p>

<p>&nbsp;</p>]]></description><pubDate>Wed, 15 Apr 2026 17:46:00 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/OPTICALLY_ENCODED_DNA_BARCODE_PARTICLES</guid><dataField:caseId>CZB-326B</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:46:00 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Aaron</dataField:firstName><dataField:lastName>Streets</dataField:lastName><dataField:title>Principal Investigator</dataField:title><dataField:department></dataField:department><dataField:emailAddress>astreets@berkeley.edu</dataField:emailAddress><dataField:phoneNumber>510-365-2564 </dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Boden</dataField:firstName><dataField:lastName>Eakins</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>eakins@berkeley.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Rodrigo</dataField:firstName><dataField:lastName>Chaves</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>rchaves@berkeley.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName></dataField:firstName><dataField:lastName>CZ Biohub Admin</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>AUTOANTIBODIES FOR AUTOIMMUNE NEUROLOGICAL DISEASE DIAGNOSIS</title><link>https://canberra-ip.technologypublisher.com/tech/AUTOANTIBODIES_FOR_AUTOIMMUNE_NEUROLOGICAL_DISEASE_DIAGNOSIS</link><description><![CDATA[<p>Researchers at UCSF have developed a novel diagnostic for autoimmune neurological diseases.</p>

<p>&nbsp;</p>

<p>Autoimmune encephalitis and ataxia are serious neurological conditions that can be life-threatening if they are not diagnosed early. Diagnosis is challenging because symptoms vary widely, imaging and lab tests are often non-specific, and these diseases can resemble other disorders. One reliable clue is the presence of immune antibodies that mistakenly target proteins in the nervous system, which can be detected in blood or cerebrospinal fluid. In some well-defined conditions, these antibodies are sufficient to make a clear diagnosis. Although many such antibody&ndash;disease links are known, a large number of cases, especially certain unexplained ataxias, likely involve immune mechanisms that have not yet been identified.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention encompasses a novel potential diagnostic avenue for patients with paraneoplastic disorders, which result from an autoimmune response, typically triggered by certain types of cancers such as small cell lung cancer. Briefly, researchers have found that autoantibodies against the protein RIMKLA in a patient&rsquo;s cerebrospinal fluid (CSF) or blood correlate with having a paraneoplastic disorder. Specifically, these antibodies seem to react with a few specific short peptide sequences within the protein with high specificity. This discovery can be used to develop novel diagnostics for paraneoplastic syndromes, for which there are currently few diagnostics. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li ><strong>Diagnostic tool for autoimmune neurological disorders: </strong>This invention comprises a novel method for the diagnosis of autoimmune neurological disorders. </li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li ><strong>Multiple diagnostic modalities: </strong>This patent allows for the use of multiple modalities for a diagnostic tool including tissue staining, cell based assays, or ELISA. </li>
	<li >&nbsp;</li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Autoimmune, Autoantibody</p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-329F</p>

<p>UCSF Ref. no. SF2025-142</p>]]></description><pubDate>Wed, 15 Apr 2026 17:44:35 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/AUTOANTIBODIES_FOR_AUTOIMMUNE_NEUROLOGICAL_DISEASE_DIAGNOSIS</guid><dataField:caseId>CZB-329F</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:44:35 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Joseph</dataField:firstName><dataField:lastName>DeRisi</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>joe@czbiohub.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Wilson</dataField:lastName><dataField:title>Professor</dataField:title><dataField:department>Neurology</dataField:department><dataField:emailAddress>Michael.Wilson@ucsf.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Caleigh</dataField:firstName><dataField:lastName>Mandel-Brehm</dataField:lastName><dataField:title>Postdoctoral Scholar</dataField:title><dataField:department>Biochemistry and Biophysics</dataField:department><dataField:emailAddress>Caleigh.Mandel-Brehm@ucsf.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Samuel</dataField:firstName><dataField:lastName>Pleasure</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>Samuel.pleasure@ucsf.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName></dataField:firstName><dataField:lastName>CZ Biohub Admin</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>PROTEIN ONLY TOPICAL VACCINES AND METHODS OF USE</title><link>https://canberra-ip.technologypublisher.com/tech/PROTEIN_ONLY_TOPICAL_VACCINES_AND_METHODS_OF_USE</link><description><![CDATA[<p>Researchers at Stanford have developed a novel vaccine strategy that would remove the need to use needles in vaccine administration.</p>

<p>Vaccination is a highly effective and affordable way to prevent disease, saving an estimated 4.4 million lives each year. However, most vaccines require injection by trained healthcare workers, which can discourage people who fear needles and complicate vaccine distribution. Needle-based delivery also limits the ability to give combination vaccines that protect against multiple viruses at once. In addition, vaccines that stimulate strong mucosal immunity to block respiratory virus transmission have been difficult to achieve, highlighting a clear gap in the market for safe, effective non-needle&ndash;based vaccination strategies.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention would allow for vaccination to occur via a topical treatment. Briefly, this topical treatment would contain a fusion protein with a binder polypeptide and an antigenic polypeptide. This binder polypeptide would be capable of binding to surface proteins on antigen presenting cells (APCs) such as a major histocompatibility complex II (MHCII) protein or an Fc receptor. By engaging with APCs present on the surface of the skin, this topical vaccine could illicit an immune (T cell or B cell) response that would confer immunity to the pathogen that is represented in the antigenic polypeptide. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li ><strong>Vaccination: </strong>A topical vaccine would allow for more widespread vaccination, especially in low resource areas where the supply chain is a limiting factor to effective population vaccination strategies. </li>
</ul>

<p><u>Advantages</u></p>

<ul>
	<li ><strong>Removes the need for needles: </strong>A topical vaccine would remove the need for the use of needles in vaccinations, which would in turn make vaccines more accessible. </li>
	<li ><strong>Ability to vaccinate for multiple viruses: </strong>Needles make it difficult to vaccinate for multiple viruses at a time due to volume constraints, a topical vaccine would make vaccinating for multiple viruses at once possible. </li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vivo</em></p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Vaccine</p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-325S</p>

<p>Stanford ref. no. S24-468</p>]]></description><pubDate>Wed, 15 Apr 2026 17:40:45 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/PROTEIN_ONLY_TOPICAL_VACCINES_AND_METHODS_OF_USE</guid><dataField:caseId>CZB-325S</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:40:45 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fischbach</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>fischbach@fischbachgroup.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Djenet</dataField:firstName><dataField:lastName>Bousbaine</dataField:lastName><dataField:title>Postdoctoral Scholar</dataField:title><dataField:department>Bioengineering</dataField:department><dataField:emailAddress>djenetb@stanford.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName></dataField:firstName><dataField:lastName>CZ Biohub Admin</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>HIGH THROUGHPUT PRODUCTION OF PROTEIN VARIANTS</title><link>https://canberra-ip.technologypublisher.com/tech/HIGH_THROUGHPUT_PRODUCTION_OF_PROTEIN_VARIANTS</link><description><![CDATA[<p>Researchers at Stanford &nbsp;have developed a novel high throughput system for the addition of amino acids into specific sites on proteins of interest. </p>

<p>Classical biochemical assays yield rigorous kinetic and thermodynamic measurements but are slow, expensive, and inherently low-throughput, limiting their use in large-scale protein variant studies. Microfluidic platforms such as MITOMI and HT-MEK address throughput and reagent constraints by enabling parallelized quantitative analysis of thousands of proteins, yet they depend on costly DNA array preparation and are largely restricted to the canonical amino acids. Genetic code expansion can introduce noncanonical amino acids and broaden protein chemical diversity, but current in vivo and in vitro implementations suffer from scalability, efficiency, and experimental-control limitations. These challenges underscore the need for scalable, integrated approaches that couple high-throughput microfluidics with expanded genetic encoding to systematically probe protein structure&ndash;function relationships.</p>

<p><u>Stage of Research</u></p>

<p>This invention yields a novel method for high-throughput production of a set of protein variants of protein(s) of interest where each of the set of protein variants independently includes one or more site-specific amino acid substitutions. Briefly, engineered DNA variants encoding a protein of interest with suppressable codons at defined positions are loaded into distinct microfluidic compartments. Subsequently, site-specific amino acid substitutions occur by adding one or more species of suppressor tRNAs that are charged with a pre-selected amino acid to the microfluidic compartments. This platform combines high throughput metholodolgy while maintaining the ability to systematically probe protein structure-function relationships. </p>

<p>The disclosure allows rapid, programmable installation of canonical or noncanonical amino acids</p>

<p>at designated sites, with precise temporal control and reduced reagent consumption,</p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li ><strong>Programmable Installation of Amino Acids: </strong>By allowing for the systematic dissection of the function of different amino acids at different positions, this method facilitates comprehensive mutagenesis and biochemical characterization in vitro</li>
	<li ><strong>Interrogation of Protein Structure-Function Relationships: </strong>Allows for the global study of how a protein&rsquo;s molecular structure, including its amino acid sequence, three-dimensional fold, and chemical features determines its biological activity, such as binding, catalysis, regulation, or stability.</li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li ><strong>Precise Temporal Control: </strong>This method allows for the ability to control precisely which position amino acids are added in any protein of interest. </li>
	<li ><strong>Reduced Reagent Consumption: </strong>Microfluidic compartmentalization allows for reaction sizes to be reduced and therefore allows for the reduced consumption of necessary reagents. </li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Protein, High throughput, Variant</p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-321S</p>

<p>Stanford ref no. S24-413</p>]]></description><pubDate>Wed, 15 Apr 2026 17:40:13 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/HIGH_THROUGHPUT_PRODUCTION_OF_PROTEIN_VARIANTS</guid><dataField:caseId>CZB-321S</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:40:13 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Patrick</dataField:firstName><dataField:lastName>Almhjell</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>almhjell@stanford.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Micah</dataField:firstName><dataField:lastName>Olivas</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Polly</dataField:firstName><dataField:lastName>Fordyce</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>pfordyce@stanford.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName></dataField:firstName><dataField:lastName>CZ Biohub Admin</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>POTENT INHIBITORS OF THE PLASMODIUM PROTEASOME AND THEIR SYNTHESIS VIA A NOVEL ROUTE</title><link>https://canberra-ip.technologypublisher.com/tech/POTENT_INHIBITORS_OF_THE_PLASMODIUM_PROTEASOME_AND_THEIR_SYNTHESIS_VIA_A_NOVEL_ROUTE</link><description><![CDATA[<p><strong>POTENT INHIBITORS OF THE PLASMODIUM PROTEASOME AND THEIR SYNTHESIS VIA A NOVEL ROUTE</strong></p>

<p>Researchers at UCSF have developed a novel treatment for the causative pathogens for both malaria and tuberculosis respectively.</p>

<p>&nbsp;</p>

<p>Tuberculosis and malaria are caused by different infectious organisms, but both remain major global infectious diease health threats. As these pathogens become more resistant to existing treatments, it is likely that infections will become more common and harder to cure. Both organisms depend on a protein-cleaning system, called the 20S proteasome subunit, to survive stressful conditions inside the human body. However, designing drugs that block this system is challenging because similar machinery exists in human cells and must be spared. This creates an urgent need for new treatments that can precisely target these pathogens without harming the patient.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention comprises a novel treatment for the causative pathogens for tuberculosis as well as malaria. Specifically, the inventors have discovered that syringolins and syringolin-like compounds are successful in inhibiting both of these pathogens. Syringolins are small peptide-like molecules with a reactive group that allows it to bind irreversibly to the proteasome. This in turn blocks the proteasome which is the cell&rsquo;s protein &ldquo;recycling&rdquo; system and is a key part of protein degradation and quality control. Syringolins and syringolin-like compounds in this invention have been shown to specifically inhibit the 20S proteasome subunit which is vital for proteasome function. Studies in cell cultures have shown that these compounds can also enhance the efficacy of known tuberculosis treatments such as pretomanid. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li >Treatment of causative pathogen of tuberculosis in humans</li>
	<li >Treatment of causative pathogen of malaria in humans</li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li >Can inhibit causative pathogen of tuberculosis when used alone or in conjunction with known tuberculosis treatments such as pretomanid</li>
	<li >Not currently widely used compounds, so little risk of drug resistance. </li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-345F</p>

<p>UCSF ref. no. SF2026-013</p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Malaria, infectious disease</p>]]></description><pubDate>Wed, 15 Apr 2026 17:39:20 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/POTENT_INHIBITORS_OF_THE_PLASMODIUM_PROTEASOME_AND_THEIR_SYNTHESIS_VIA_A_NOVEL_ROUTE</guid><dataField:caseId>CZB-345F</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:39:20 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Bonnevie</dataField:firstName><dataField:lastName>Bernardino</dataField:lastName><dataField:title>IP Paralegal</dataField:title><dataField:department>Biohub Network</dataField:department><dataField:emailAddress>bonnevie.bernardino@czbiohub.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>Universal Chromatin Regulators as Transcriptional Modifiers Across Eukaryotes</title><link>https://canberra-ip.technologypublisher.com/tech/Universal_Chromatin_Regulators_as_Transcriptional_Modifiers_Across_Eukaryotes</link><description><![CDATA[<p><strong>CHROMATIN REGULATORS AS TRANSCRIPTIONAL MODIFIERS ACROSS EUKARYOTES</strong></p>

<p>Researchers at Berkeley and LBNL have developed a novel method for modifying gene transcription.</p>

<p>&nbsp;</p>

<p>In eukaryotic cells, DNA is packaged into chromatin, a dynamic structure that can shift between more open (euchromatin) and condensed (heterochromatin) states to regulate processes like gene expression, DNA repair, and genome organization. This regulation is controlled by chromatin regulators, i.e. proteins that add, remove, or interpret epigenetic modifications, as well as remodel chromatin structure, working alongside transcription factors. These mechanisms are highly conserved across diverse eukaryotic species, underscoring their fundamental biological importance. However, experimentally testing the full function of these proteins remains challenging. Current high-throughput approaches often rely on protein fragments rather than full-length chromatin regulators, which can miss key functional domains and enzymatic activities. Additionally, most chromatin engineering has been developed in a few model systems, creating a need for more versatile tools that can function across a broader range of organisms, including plants and other less-studied eukaryotes.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention comprises a chromatin regulator protein fused to a DNA-binding protein that in turn modifies gene transcription. The inventors used a multi-kingdom, full length chromatin regulator (CR) library to uncover several potent chromatin regulator proteins. These proteins include the human proteins SAP25, MBD3, RCOR1, MTA2, WDR82, DPY30, the plant proteins CMT3, SWC2, or the yeast proteins CHZ1, IES5, and TTI1 respectively. These proteins are then fused to DNA binding proteins with the product of that fusion being referred to as CR fusion proteins. These CR fusion proteins are then able to proteins to increase or decrease transcription of specific genes in eukaryotic cells when introduced to cells with specific nucleic acids. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li >Specific modification of transcription of specific proteins in eukaryotic cells</li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li >Can be used in a broad range of eukaryotic cell types across biological kingdoms</li>
	<li >Utilizes full length chromatin regulators rather than fragments</li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-343B</p>

<p>Berkeley ref. no. BK-2026-011</p>

<p>LBNL ref. no. 2025-170</p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Chromatin, nucleic acid</p>]]></description><pubDate>Wed, 15 Apr 2026 17:39:03 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/Universal_Chromatin_Regulators_as_Transcriptional_Modifiers_Across_Eukaryotes</guid><dataField:caseId>CZB-343B</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:39:03 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Bonnevie</dataField:firstName><dataField:lastName>Bernardino</dataField:lastName><dataField:title>IP Paralegal</dataField:title><dataField:department>Biohub Network</dataField:department><dataField:emailAddress>bonnevie.bernardino@czbiohub.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title><![CDATA[Diagnostic & prognostic immune markers for critical infections]]></title><link>https://canberra-ip.technologypublisher.com/tech?title=Diagnostic_%2b_prognostic_immune_markers_for_critical_infections</link><description><![CDATA[<p><strong>DIAGNOSTIC AND PROGNOSTIC IMMUNE MARKERS FOR CRITICAL INFECTIONS</strong></p>

<p>Researchers at UCSF have discovered novel biomarkers for respiratory infections.</p>

<p>&nbsp;</p>

<p>Respiratory infections, like pneumonia, bronchitis, and viral illnesses, are a major global health problem, ranging from mild colds to serious conditions that require hospitalization. Infections in the lungs, especially pneumonia, are a leading cause of death and hospital stays, particularly for children, older adults, and those with weakened immune systems. These infections can sometimes lead to sepsis, a dangerous condition where the body&rsquo;s response to infection damages its own organs and can quickly become life-threatening. Sepsis often develops rapidly and requires urgent treatment, and recovery can result in lasting health effects. Despite medical advances, diagnosing these infections and predicting outcomes remains difficult, as current tests can be slow or inaccurate, highlighting the need for faster and more reliable tools to guide treatment.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention details biomarkers for diagnosis of respiratory infection and/or sepsis. Briefly, specific biomarkers are measured by obtaining a biological sample from subject using an ELISA or other biomarker detection method. Subsequently, concentrations of several separate biomarkers in specimens are collated and a probability score is calculated to indicate how likely a subject is to develop a lower respiratory tract infection and/or sepsis. This method has the potential to indicate the severity of sepsis, classify the infection into clinically relevant disease groups, estimate the subject&#39;s survival rate, and predict the likelihood of benefit from specific treatments (such as corticosteroids) based on the expression profile.</p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li >Prediction of likelihood of the development of sepsis and the severity of sepsis</li>
	<li >Prediction of clinical response to specific pharmacologic agents </li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li >High sensitivity and specificity</li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-342F</p>

<p>UCSF ref. no. SF2025-232</p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Sepsis, diagnosis, respiratory</p>]]></description><pubDate>Wed, 15 Apr 2026 17:30:53 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech?title=Diagnostic_%2b_prognostic_immune_markers_for_critical_infections</guid><dataField:caseId>CZB-342F</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:30:53 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Annette</dataField:firstName><dataField:lastName>Parent</dataField:lastName><dataField:title> </dataField:title><dataField:department> </dataField:department><dataField:emailAddress>annette.parent@czbiohub.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>SYRINGOLINS AS INHIBITORS OF THE MYCOBATERIAL PROTEASOME</title><link>https://canberra-ip.technologypublisher.com/tech/SYRINGOLINS_AS_INHIBITORS_OF_THE_MYCOBATERIAL_PROTEASOME</link><description><![CDATA[<p><strong>SYRINGOLINS AS INHIBITORS OF THE MYCOBACTERIAL PROTEASOME</strong></p>

<p>Researchers at UCSF have discovered a novel prospective compound for the treatment of tuberculosis.</p>

<p>&nbsp;</p>

<p>Tuberculosis is caused by the bacterium <em>Mycobacterium tuberculosis</em> (Mtb) and is one of the deadliest infectious diseases worldwide. As more strains become resistant to existing drugs, it&rsquo;s expected that tuberculosis cases will become harder to treat, increasing the need for new medications. Scientists have found that the bacterium relies on a structure called the 20S proteasome to survive, especially under stressful conditions inside the human body. However, targeting this structure is difficult because similar systems exist in human cells, so treatments must specifically affect the bacteria without harming the patient. Overall, there is a strong need to develop new drugs that can safely and effectively kill the tuberculosis bacterium.</p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention comprises a novel therapeutic treatment for Mtb. Specifically, the inventors have discovered that syringolins and syringolin-like compounds are successful in inhibiting Mtb, the causative bacterium for tuberculosis in humans. Syringolins are small peptide-like molecules with a reactive group that allows it to bind irreversibly to the proteasome. This in turn blocks the proteasome which is the cell&rsquo;s protein &ldquo;recycling&rdquo; system and is a key part of protein degradation and quality control. Studies in cell cultures have shown that syringolins can also enhance the efficacy of known Mtb treatments such as pretomanid. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li >Treatment of tuberculosis in humans</li>
</ul>

<p >&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li >Can inhibit Mtb when used alone or in conjunction with known Mtb treatments such as pretomanid</li>
	<li >Not currently widely used compounds, so little risk of Mtb drug resistance </li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-338F</p>

<p>UCSF ref. no. SF-2025-196</p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p>Infectious disease, bacteria, therapeutic</p>]]></description><pubDate>Wed, 15 Apr 2026 17:29:34 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/SYRINGOLINS_AS_INHIBITORS_OF_THE_MYCOBATERIAL_PROTEASOME</guid><dataField:caseId>CZB-338F</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 17:29:34 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Annette</dataField:firstName><dataField:lastName>Parent</dataField:lastName><dataField:title> </dataField:title><dataField:department> </dataField:department><dataField:emailAddress>annette.parent@czbiohub.org</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>PHOTOCLEAVABLE INTERFERING GUIDE RNAS</title><link>https://canberra-ip.technologypublisher.com/tech/PHOTOCLEAVABLE_INTERFERING_GUIDE_RNAS</link><description><![CDATA[<p><strong>PHOTOCLEAVABLE INTERFERING GUIDE RNAS AND USE THEREOF</strong></p>

<p>Researchers at Berkeley have developed a novel method of light sensitive control of Cas proteins.</p>

<p>&nbsp;</p>

<p>CRISPR-based diagnostic tools can detect DNA or RNA with high sensitivity and specificity. In these systems, enzymes like Cas13a use a guide RNA to find a matching target sequence, which activates the enzyme to cut nearby RNA molecules. This cutting activity is used to generate a fluorescent signal, allowing detection of the target. However, the system can produce background signals even without a target, and it can be difficult to separate signals when testing for multiple targets at once. Improving the ability to distinguish true signals from background noise is a key challenge for making these diagnostics more reliable. </p>

<p>&nbsp;</p>

<p><u>Stage of Research</u></p>

<p>This invention comprises a novel method to achieve precise spatio-temporal activity of Cas13a activity using light. Briefly, a single photo-cleavable/photodegradable component that links a canonical cRNA to an interfering DNA segment that suppresses the trans-cleavage activity of Casi3a. Prior to light exposure, activity of Cas13 is inhibitied even in the presence of activating (target) RNA molecules. Upon brief light exposure the Cas13a activity rapidly recovers to the full rate for a given guide-target combination. Several levers exist within this system, specifically the length of interfering DNA segment and the intensity of light, which tune the degree of suppression and the level trans-cleavage activity before and after light exposure, respectively. </p>

<p>&nbsp;</p>

<p><u>Applications</u></p>

<ul>
	<li >Precise spatio-temporal control of Casl3a assay in droplets</li>
	<li >Co-infection models where two viruses can be detected in a single reaction with accurate estimates of the relative concentrations of both viral RNAs present. </li>
</ul>

<p>&nbsp;</p>

<p><u>Advantages</u></p>

<ul>
	<li >Improved signal to background ratios in thedetection of positive droplets.</li>
	<li >Spatiotemporal control of multiple items in a single reaction. </li>
</ul>

<p >&nbsp;</p>

<p><u>Stage of Development</u></p>

<p>Research- <em>in vitro</em></p>

<p>&nbsp;</p>

<p><u>Technology Reference</u></p>

<p>CZ Biohub ref. no. CZB-334B</p>

<p>Berkeley Ref. no. BK-2025-117</p>

<p>&nbsp;</p>

<p><u>Keywords</u></p>

<p class="p1">CRISPR, Photodegradable</p>]]></description><pubDate>Wed, 15 Apr 2026 16:51:03 GMT</pubDate><author>Bonnevie.Bernardino@czbiohub.org</author><guid>https://canberra-ip.technologypublisher.com/tech/PHOTOCLEAVABLE_INTERFERING_GUIDE_RNAS</guid><dataField:caseId>CZB-334B</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 16:51:03 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Daniel</dataField:firstName><dataField:lastName>Fletcher</dataField:lastName><dataField:title></dataField:title><dataField:department>Bioengineering Department Operations</dataField:department><dataField:emailAddress>fletch@berkeley.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Deepak</dataField:firstName><dataField:lastName>Krishnamurthy</dataField:lastName><dataField:title></dataField:title><dataField:department>The California Institute for Quantitative Biosciences (QB3)</dataField:department><dataField:emailAddress>deepak90@berkeley.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Carlos</dataField:firstName><dataField:lastName>Pitti</dataField:lastName><dataField:title></dataField:title><dataField:department>The California Institute for Quantitative Biosciences (QB3)</dataField:department><dataField:emailAddress>cngpit@berkeley.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName></dataField:firstName><dataField:lastName>CZ Biohub Admin</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Biology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>Method and Compositions for Modulating PPAR activity in ISCs</title><link>https://canberra-ip.technologypublisher.com/tech/Method_and_Compositions_for_Modulating_PPAR_activity_in_ISCs</link><description><![CDATA[<div ><strong>Invention Description</strong></div>

<div >Diet profoundly impacts our nutritional landscape, public health, and disease susceptibility. In the gut, nutrients directly influence how intestinal stem cells (ISCs) function and maintain homeostasis. Yet, the connection between metabolic processes and transcriptional regulation are poorly defined. As a long-lived population, adult ISCs maintain the intestinal lining through self-renewal and differentiation. Because they are directly exposed to nutrients within the intestinal crypt, ISCs actively adapt their metabolic processes and fate decisions in response to changes in nutrient availability.</div>

<div >&nbsp;</div>

<div >Researchers at Arizona State University have elucidated how O-GlcNAcylation (OGN) serves as a metabolic signaling mechanism in intestinal stem cells (ISCs), integrating glucose and lipid metabolism to regulate mitochondrial function and stem cell behavior via PPAR signaling pathways. Dietary factors such as a high-fat diet alter OGN levels in ISC mitochondria, influencing proliferation and regenerative capacity and this dynamic regulation impacts ISC transcriptional programs and tissue homeostasis. Further, novel compositions were developed for metabolic control of ISC function.</div>

<div >&nbsp;</div>

<div >This technology provides novel methods and compositions to regulate ISC metabolic programming through PPAR signaling influenced by dietary nutrients.</div>

<div >&nbsp;</div>

<div ><strong>Potential Applications</strong></div>

<ul>
	<li >Development of diagnostics and therapies for intestinal diseases and tissue regeneration</li>
	<li >Design of metabolic-based interventions to control stem cell proliferation</li>
	<li >Creation of dietary supplements or drugs modulating O-GlcNAcylation pathways</li>
	<li >Research tools for studying mitochondrial metabolism and stem cell biology</li>
	<li >Personalized nutrition solutions impacting stem cell and tissue health</li>
</ul>

<div ><strong>Benefits and Advantages</strong></div>

<ul>
	<li >Enables dynamic integration of glucose and lipid metabolism in ISCs</li>
	<li >Highlights a novel regulatory axis for metabolic and transcriptional control</li>
	<li >Utilizes advanced MITO-Tag model for precise mitochondrial isolation</li>
	<li >Offers potential for modulating stem cell function through metabolic pathways</li>
	<li >Improves understanding of how diet influences stem cell behavior and tissue regeneration</li>
</ul>

<div >For more information about this opportunity, please see</div>

<div ><a href="https://www.biorxiv.org/content/10.64898/2026.03.13.711696v1" target="_blank">Hartley McDermott et al &ndash; bioRxiv &ndash; 2026</a></div>]]></description><pubDate>Wed, 15 Apr 2026 16:47:24 GMT</pubDate><author>ip@skysonginnovations.com</author><guid>https://canberra-ip.technologypublisher.com/tech/Method_and_Compositions_for_Modulating_PPAR_activity_in_ISCs</guid><dataField:caseId>M26-024L</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 16:47:24 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Thomas</dataField:firstName><dataField:lastName>Hartley McDermott</dataField:lastName><dataField:title>Graduate Student</dataField:title><dataField:department>Sols Graduate Programs</dataField:department><dataField:emailAddress>thartle3@asurite.asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Miyeko</dataField:firstName><dataField:lastName>Mana</dataField:lastName><dataField:title>Asst Professor</dataField:title><dataField:department><![CDATA[Sols Administration & Faculty]]></dataField:department><dataField:emailAddress>Miyeko.Mana@asu.edu</dataField:emailAddress><dataField:phoneNumber>4807275845</dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jovan</dataField:firstName><dataField:lastName>Heusser</dataField:lastName><dataField:title>Director of Licensing and Business Development</dataField:title><dataField:department></dataField:department><dataField:emailAddress>jovan.heusser@skysonginnovations.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Bioanalytical Assays, Chemistries & Devices| Biomaterials| Life Science (All LS Techs)]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Rapid Detection of an Anthrax Biomarker by Surface-Enhanced Raman Spectroscopy</title><link>https://canberra-ip.technologypublisher.com/tech/Rapid_Detection_of_an_Anthrax_Biomarker_by_Surface-Enhanced_Raman_Spectroscopy</link><description><![CDATA[<h2>NU 2006-092</h2>

<h3>Inventors</h3>

<ul>
	<li>Richard Van Duyne*</li>
	<li>Olga Lyandres</li>
	<li>Matthew Young</li>
	<li>Xiaoyu Zhang</li>
	<li>Alyson Whitney</li>
	<li>Jing Zhao</li>
	<li>Jeffrey Elam</li>
</ul>

<h3>Short Description</h3>

<p >Highly sensitive biosensor for detection of anthrax-causing bacterium with field use capabilities</p>

<h3>Abstract</h3>

<p >Northwestern researchers have created a surface-enhanced Raman biosensor for use in detecting and identifying Bacillus anthracis, a spore-forming bacterium and dangerous pathogen that causes anthrax. B. subtilis spores, harmless simulants for B. anthracis, were detected using surface-enhanced Raman spectroscopy (SERS) on silver film over nanosphere (AgFON) substrates. Calcium dipicolinate (CaDPA), a biomarker for Bacillus spores, was efficiently extracted by sonication in nitric acid and rapidly detected by SERS. Improved binding efficiency of the CaDPA adsorption is accomplished by using atomic layer deposition (ALD) to coat the AgFON surface with a layer of alumina, which also protects the underlying noble metal surface. The speed and sensitivity of this SERS sensor indicate its usefulness for the field analysis of other potentially harmful environmental agents as well. The sensing capabilities of this technology can be readily incorporated into a field-portable instrument, which enables a rapid, sensitive and portable detection protocol suitable for use by first responders.</p>

<h3>Applications</h3>

<ul>
	<li>Biosensor for microorganisms</li>
</ul>

<h3>Advantages</h3>

<ul>
	<li>Efficient platform</li>
	<li>High sensitivity</li>
	<li>Rapid detection of microorganisms</li>
	<li>Readily compatible into a field-portable instrument</li>
</ul>

<h3>Publications</h3>

<p >Zhang X, Zhao J, Whitney AV, Elam JW, Van Duyne RP (2006) <a href="https://pubs.acs.org/doi/10.1021/ja0638760" target="_blank">Ultrastable substrates for surface-enhanced Raman spectroscopy: Al2O3 overlayers fabricated by atomic layer deposition yield improved anthrax biomarker detection</a>. <em>Journal of the American Chemical Society</em>. 128(31): 10304-9.</p>

<p >Zhang X, Young MA, Lyandres O, Van Duyne RP (2005) <a href="https://pubs.acs.org/doi/10.1021/ja043623b" target="_blank">Rapid detection of an anthrax biomarker by surface-enhanced Raman spectroscopy</a>. <em>Journal of the American Chemical Society</em>. 127(12): 4484-9.</p>

<h3>IP Status</h3>

<p >Issued US patent number 8,628,727</p>]]></description><pubDate>Wed, 15 Apr 2026 13:54:46 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Rapid_Detection_of_an_Anthrax_Biomarker_by_Surface-Enhanced_Raman_Spectroscopy</guid><dataField:caseId>2006-092</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 13:54:46 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Devices, Diagnostics, Health IT, Imaging, Medical device, Sensors, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Arjan</dataField:firstName><dataField:lastName>Quist</dataField:lastName><dataField:title>Executive Director of Innovation Management</dataField:title><dataField:department>Innovation and New Ventures</dataField:department><dataField:emailAddress>arjan.quist@northwestern.edu</dataField:emailAddress><dataField:phoneNumber>847/467-0305</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Healthcare Devices, Tools & IT]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>A Method to Treat Neurodegenerative Diseases</title><link>https://canberra-ip.technologypublisher.com/tech/A_Method_to_Treat_Neurodegenerative_Diseases</link><description><![CDATA[<p>This innovation is a method and composition for treating, preventing, or delaying the progression of neurodegenerative diseases using cell type-specific gene therapy. The therapy is delivered to human or veterinary subjects using an adeno-associated virus (AAV) vector that carries the peroxisome proliferator-activated receptor alpha (PPARA) gene. The focus of this therapeutic is on the role of astrocytes, a type of cell in the brain that supports and interacts with neurons. The researchers have developed an AAV vector that specifically targets and upregulates the expression of the mouse Ppara gene in astrocytes, while not affecting other cell types in the brain. By increasing the activity of fatty acid (FA) degradation in astrocytes, the treatment aims to restore lipid balance and alleviate the detrimental effects of lipid dysregulation observed in neurodegenerative diseases. In preclinical studies using a mouse model of AD, this treatment has shown promising results, including reduced beta-amyloid plaque accumulation, improved synaptic plasticity, and cognitive function. The novelty of this technology lies in the combination of specific AAV vector serotypes, a promoter with high astrocyte specificity, and the target gene PPARA, which together provide an efficient and targeted approach to treating neurodegenerative diseases characterized by lipid dysregulation.<br />
<br />
<strong>Background:&nbsp;</strong><br />
Current treatment approaches for neurodegenerative diseases include pharmaceutical interventions, such as cholinesterase inhibitors and NMDA receptor antagonists, which provide symptomatic relief but do not address the underlying factor of lipid dysregulation. Other approaches, such as gene therapies, have been explored, but they often lack cell type specificity, leading to unintended effects and potential side effects. This lack of cell type-specific targeting and intervention leads to limited effectiveness and suboptimal outcomes in halting disease progression and improving cognitive function. By specifically targeting and upregulating PPARA expression in astrocytes, this treatment directly addresses the impaired fatty acid degradation in these cells, providing a precise and efficient way to restore lipid balance and mitigate the detrimental effects on neuronal health and cognitive function.&nbsp;<br />
<br />
<strong>Applications:&nbsp;</strong></p>

<ul>
	<li>Treatment for neurodegenerative diseases&nbsp;
	<ul>
		<li>Alzheimer&#39;s Disease&nbsp;</li>
		<li>Parkinson&rsquo;s Disease</li>
	</ul>
	</li>
</ul>

<p><br />
<strong>Advantages:&nbsp;</strong></p>

<ul>
	<li>Cell type-specific targeted treatment&nbsp;</li>
	<li>Mitigates detrimental effects on neuronal health</li>
	<li>Improved synaptic plasticity&nbsp;</li>
	<li>Reduced beta-amyloid plaque accumulation</li>
	<li>Improved cognitive function</li>
	<li>Mouse model data with promising results</li>
</ul>]]></description><pubDate>Wed, 15 Apr 2026 13:53:21 GMT</pubDate><author>JianlingL@tla.arizona.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/A_Method_to_Treat_Neurodegenerative_Diseases</guid><dataField:caseId>UA23-256</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 13:53:21 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Fei</dataField:firstName><dataField:lastName>Yin</dataField:lastName><dataField:title>Asst. Professor</dataField:title><dataField:department>CIBS, Health Science</dataField:department><dataField:emailAddress>feiyin@email.arizona.edu</dataField:emailAddress><dataField:phoneNumber>520-626-4102</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Weihua</dataField:firstName><dataField:lastName>Wang</dataField:lastName><dataField:title>Senior research specialist</dataField:title><dataField:department>UAHS Brain Science</dataField:department><dataField:emailAddress>weihuawang@arizona.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Mitch</dataField:firstName><dataField:lastName>Graffeo</dataField:lastName><dataField:title>Sr. Licensing Manager - COM-T</dataField:title><dataField:department></dataField:department><dataField:emailAddress>mitchg@tla.arizona.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Life Sciences| Technology Classifications > Healthcare Portfolios > Neurology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Gallium Oxide Trench Junction Barrier Schottky Diodes</title><link>https://canberra-ip.technologypublisher.com/tech/Gallium_Oxide_Trench_Junction_Barrier_Schottky_Diodes</link><description><![CDATA[<div ><strong>Invention Description</strong></div>

<div >High-voltage power electronic devices require materials and designs that can handle large electric fields while maintaining low power loss and high efficiency. Traditional diode structures often face trade-offs between breakdown voltage, leakage current, and on-resistance, limiting their performance in demanding applications. As power systems continue to scale, there is a need for devices that can achieve higher breakdown voltages without sacrificing efficiency or increasing energy loss. This highlights the demand for advanced semiconductor designs that improve electric field management and overall device reliability.</div>

<div >&nbsp;</div>

<div >Researchers at Arizona State University have developed a vertical gallium oxide (&beta;-Ga₂O₃) trench junction barrier Schottky diode (JBSD) incorporating p-type nickel oxide (NiO) and a space-modulated junction termination extension (SM-JTE). Using a novel bi-layer hard mask process, NiO is deposited along trench sidewalls to improve electric field distribution within the device. This design enables significantly higher reverse breakdown voltages (~2 kV) and lower turn-on voltages (~1 V) compared to conventional planar diodes. The trench SM-JTE structure reduces leakage current and conduction losses while maintaining low on-resistance. Together, these improvements offer enhanced performance for next-generation high-voltage power electronics.</div>

<div >This novel gallium oxide trench junction barrier Schottky diode design uses p-type nickel oxide with space modulated junction termination extension to achieve high breakdown voltage and low turn-on voltage for advanced power device applications.</div>

<div >&nbsp;</div>

<div ><strong>Potential Applications</strong></div>

<ul>
	<li >High-voltage, low-loss power electronics</li>
	<li >Power switches and rectifiers for electric vehicles and renewable energy systems</li>
	<li >Next-generation, energy-efficient power conversion systems</li>
	<li >High-efficiency power supplies and inverters requiring ultrahigh voltage blocking capability</li>
	<li >Advanced semiconductor components for smart grid and energy infrastructure</li>
	<li >Military and aerospace electronics demanding robust, high-power semiconductor devices</li>
</ul>

<div ><strong>Benefits and Advantages</strong></div>

<ul>
	<li >High reverse breakdown voltage exceeding 1.8 kV with peak values near 2 kV</li>
	<li >Low turn-on voltage around 1 V, reduced from ~2.5 V in planar devices</li>
	<li >Reduced conduction losses due to lower effective on-resistance</li>
	<li >Improved electric field management with trench space modulated junction termination extension</li>
	<li >Fabrication method using novel bi-layer Ni/SiO2 hard mask enabling precise NiO deposition on trench sidewalls</li>
	<li >High BFOM indicating excellent device efficiency</li>
	<li >Compatibility with scalable, cost-effective fabrication processes using halide vapor phase epitaxy (HVPE) grown &beta;-Ga2O3</li>
</ul>

<div >For more information about this opportunity, please see</div>

<div ><a href="https://pubs.aip.org/aip/aed/article/2/1/016106/3378206/Demonstration-of-KV-class-Ga2O3-trench-junction" target="_blank">Gilankar et al - APL Electron. Device - 2026</a></div>]]></description><pubDate>Wed, 15 Apr 2026 12:36:36 GMT</pubDate><author>ip@skysonginnovations.com</author><guid>https://canberra-ip.technologypublisher.com/tech/Gallium_Oxide_Trench_Junction_Barrier_Schottky_Diodes</guid><dataField:caseId>M25-325P^</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 12:36:36 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Nidhin Kurian</dataField:firstName><dataField:lastName>Kalarickal</dataField:lastName><dataField:title>Assistant Professor</dataField:title><dataField:department><![CDATA[Sch Elect Comptr & Energy Engr]]></dataField:department><dataField:emailAddress>Nidhin.Kurian.Kalarickal@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Advait</dataField:firstName><dataField:lastName>Gilankar</dataField:lastName><dataField:title>Graduate Service Assistant</dataField:title><dataField:department>School of Electrical, Computing and Energy Engineering Research</dataField:department><dataField:emailAddress>agilanka@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Physical Sciences</dataField:firstName><dataField:lastName>Team</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Advanced Materials/Nanotechnology| Energy & Power| Microelectronics| Physical Science| Semiconductors, Materials & Processes]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Fluorescent Peptides for Membrane Tension Reporting and Biomarkers</title><link>https://canberra-ip.technologypublisher.com/tech/Fluorescent_Peptides_for_Membrane_Tension_Reporting_and_Biomarkers</link><description><![CDATA[<p >A peptide-based probe technology that enables real-time, non-invasive fluorescent detection and quantitation of cell membrane tension.&nbsp;</p>

<p >Background:<br />
The 2021 Nobel Prize in Physiology or Medicine was awarded for the discovery of Piezo channels, mechanosensitive ion channels that respond to cell membrane tension, translating mechanical force directly into electro-chemical signals. Piezo channels are involved in many normal physiological processes including sensing of touch, nociception, proprioception, control of cell volume and blood pressure, sensing fullness via stretch reception in the intestine and bladder, maintenance and remodeling of bone, epithelial and vascular tissues. They are also implicated in pathologies like cancer metastasis and Alzheimer&rsquo;s Disease. Despite considerable interest in these diseases and molecular pathways, research has historically been limited to highly technical biophysical labs due to the need for complex, low-throughput electrophysiology for monitoring channel activity, and advanced microscopy methods such as FLIM and FRET for measurement of membrane tension.</p>

<p ></p>

<p >Technology Overview:&nbsp;<br />
This novel peptide probe developed by University at Buffalo researchers is a fluorescent analog of the non-toxic inhibitor of Piezo channels, GsMTx4. It takes advantage of the well-defined tension-dependent mobility of the peptide in membranes to provide a quantitative measure of membrane tension that can be measured via simple visible light fluorescence microscopy without the need for advanced hardware or complex biophysical or microscopy techniques. With increasing tension in lipid bilayers, the probe penetrates more deeply into the hydrophobic environment of the membrane, increasing the quantum yield and brightness of attached fluorophores. A major advantage of this peptide over existing probes is that its sensing occurs in the dynamic range of the native Piezo channel and at non-inhibitory concentrations, enabling a proxy measure of Piezo activation. The probes are also simple to manufacture and are expected to be dramatically more cost effective than existing market technologies for membrane tension reporting.<br />
&nbsp;</p>

<p >https://buffalo.technologypublisher.com/files/sites/7525_inpart_image.jpg</p>

<p >Please note, header image is purely illustrative. Source: Kateryna_Kon, Adobe Stock.</p>

<p >Advantages:&nbsp;<br />
</p>

<ul>
	<li>Real-time high-throughput monitoring of membrane tension</li>
	<li>Sensitive to membrane tension relevant to normal physiology</li>
	<li>Simple and cost effective&nbsp;</li>
	<li>Non-invasive - sensitive detection at concentrations that don&rsquo;t interfere with Piezo channel function</li>
	<li>Compatible with two-photon microscopy for deep tissue imaging</li>
</ul>

<p >&nbsp;</p>

<p >Applications:&nbsp;</p>

<p ></p>

<ul>
	<li>Cell biology research for processes that involve membrane dynamics, e.g. wound healing, viral infection, endocytosis and membrane trafficking, cell motility, cancer invasion and metastasis</li>
	<li>Membrane dynamics readout for high-throughput drug screening&nbsp;</li>
	<li>Assays for liposome / LNP size and composition</li>
</ul>

<p >&nbsp;</p>

<p >Intellectual Property Summary:<br />
Provisional patent application filed</p>

<p >Stage of Development:<br />
</p>

<ul>
	<li>Proof of concept, biophysics validation</li>
	<li>TRL 3</li>
</ul>

<p ></p>

<p >Licensing Status:<br />
Available for licensing or collaboration</p>

<p >Licensing Potential:</p>

<p >Development partner &ndash; Commercial partner &ndash; Exclusive or non-exclusive</p>

<p >Additional Information:&nbsp;<br />
<a href="https://www.biorxiv.org/content/10.64898/2025.12.30.697119v1" target="_blank">BioRxiv article available here</a></p>

<p >https://buffalo.technologypublisher.com/files/sites/7525_pic_11.jpg</p>

<p >&copy;2025, Research Foundation for the State University of New York</p>]]></description><pubDate>Wed, 15 Apr 2026 08:47:04 GMT</pubDate><author>techtransfer@buffalo.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Fluorescent_Peptides_for_Membrane_Tension_Reporting_and_Biomarkers</guid><dataField:caseId>030-7525</dataField:caseId><dataField:lastUpdateDate>Thu, 16 Apr 2026 06:44:27 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>A peptide-based probe technology that enables real-time, non-invasive fluorescent detection and quantitation of cell membrane tension.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background><![CDATA[The 2021 Nobel Prize in Physiology or Medicine was awarded for the discovery of Piezo channels, mechanosensitive ion channels that respond to cell membrane tension, translating mechanical force directly into electro-chemical signals. Piezo channels are involved in many normal physiological processes including sensing of touch, nociception, proprioception, control of cell volume and blood pressure, sensing fullness via stretch reception in the intestine and bladder, maintenance and remodeling of bone, epithelial and vascular tissues. They are also implicated in pathologies like cancer metastasis and Alzheimer&rsquo;s Disease. Despite considerable interest in these diseases and molecular pathways, research has historically been limited to highly technical biophysical labs due to the need for complex, low-throughput electrophysiology for monitoring channel activity, and advanced microscopy methods such as FLIM and FRET for measurement of membrane tension.</p>

<p style="font-family:Times New Roman; font-size:12pt">]]></dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology><![CDATA[This novel peptide probe developed by University at Buffalo researchers is a fluorescent analog of the non-toxic inhibitor of Piezo channels, GsMTx4. It takes advantage of the well-defined tension-dependent mobility of the peptide in membranes to provide a quantitative measure of membrane tension that can be measured via simple visible light fluorescence microscopy without the need for advanced hardware or complex biophysical or microscopy techniques. With increasing tension in lipid bilayers, the probe penetrates more deeply into the hydrophobic environment of the membrane, increasing the quantum yield and brightness of attached fluorophores. A major advantage of this peptide over existing probes is that its sensing occurs in the dynamic range of the native Piezo channel and at non-inhibitory concentrations, enabling a proxy measure of Piezo activation. The probes are also simple to manufacture and are expected to be dramatically more cost effective than existing market technologies for membrane tension reporting.<br />]]></dataField:Technology><dataField:Picture>https://buffalo.technologypublisher.com/files/sites/7525_inpart_image.jpg</dataField:Picture><dataField:PictureRef>Please note, header image is purely illustrative. Source: Kateryna_Kon, Adobe Stock.</dataField:PictureRef><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[</p>

<ul>
	<li>Real-time high-throughput monitoring of membrane tension</li>
	<li>Sensitive to membrane tension relevant to normal physiology</li>
	<li>Simple and cost effective&nbsp;</li>
	<li>Non-invasive - sensitive detection at concentrations that don&rsquo;t interfere with Piezo channel function</li>
	<li>Compatible with two-photon microscopy for deep tissue imaging</li>
</ul>

<p style="font-family:Times New Roman; font-size:12pt">]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[</p>

<ul>
	<li>Cell biology research for processes that involve membrane dynamics, e.g. wound healing, viral infection, endocytosis and membrane trafficking, cell motility, cancer invasion and metastasis</li>
	<li>Membrane dynamics readout for high-throughput drug screening&nbsp;</li>
	<li>Assays for liposome / LNP size and composition</li>
</ul>

<p style="font-family:Times New Roman; font-size:12pt">]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus>Provisional patent application filed</dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment><![CDATA[</p>

<ul>
	<li>Proof of concept, biophysics validation</li>
	<li>TRL 3</li>
</ul>

<p style="font-family:Times New Roman; font-size:12pt">]]></dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>Available for licensing or collaboration</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential><![CDATA[Development partner &ndash; Commercial partner &ndash; Exclusive or non-exclusive]]></dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo><![CDATA[<a href="https://www.biorxiv.org/content/10.64898/2025.12.30.697119v1" target="_blank">BioRxiv article available here</a>]]></dataField:AdditionalInfo><dataField:Picture2>https://buffalo.technologypublisher.com/files/sites/7525_pic_11.jpg</dataField:Picture2><dataField:PictureRef2><![CDATA[&copy;2025, Research Foundation for the State University of New York]]></dataField:PictureRef2><dataField:inventorList><dataField:inventor><dataField:firstName>Thomas</dataField:firstName><dataField:lastName>Suchyna</dataField:lastName><dataField:title>Research Assoc. Professor</dataField:title><dataField:department>Physiology and Biophysics</dataField:department><dataField:emailAddress>suchyna@buffalo.edu</dataField:emailAddress><dataField:phoneNumber>716-829-5156</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Sergei</dataField:firstName><dataField:lastName>Sukharev</dataField:lastName><dataField:title></dataField:title><dataField:department>Biology</dataField:department><dataField:emailAddress>sukharev@umd.edu</dataField:emailAddress><dataField:phoneNumber>301.405.6912</dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Featured, Research Tool, Technologies, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>David</dataField:firstName><dataField:lastName>du Plessis</dataField:lastName><dataField:title>Licensing Manager</dataField:title><dataField:department></dataField:department><dataField:emailAddress>ddupless@buffalo.edu</dataField:emailAddress><dataField:phoneNumber>716-881-7542</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > University at Buffalo| Technology Classifications| Technology Classifications > Research Tools and Reagents| Technology Classifications > Screens and Assays| Technology Classifications > Biological Materials]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Electroless Plating Solution for Forming Metal Films on Inert Substrates (Case No. 2026-211)</title><link>https://canberra-ip.technologypublisher.com/tech/Electroless_Plating_Solution_for_Forming_Metal_Films_on_Inert_Substrates_(Case_No._2026-211)</link><description><![CDATA[<p><strong>Summary:</strong><br />
<br />
UCLA researchers in the Department of Chemistry &amp; Biochemistry have developed a novel electroless plating solution that facilitates metal deposition on inert polymers without conventional pre-treatment.</p>

<p><strong>Background: </strong><br />
<br />
Metal thin films deposited on inert polymer substrates are critical components in wearable electronics, sensors, and flexible electrodes. To create high purity and uniform polymer-metal thin-film composites, chemical vapor deposition (CVD) and physical vapor deposition (PVD) are utilized. While capable of producing high-quality films, these techniques typically require vacuum systems, elevated temperatures, and capital-intensive equipment, limiting compatibility with flexible substrates and increasing manufacturing costs. Electroless plating has shown promise as a solution-based technique that enables metal film deposition on chemically inert substrates via redox reactions, without the need for an external current. Despite this, electroless plating has significant limitations. Sensitization, a critical step in deposition, relies on acidic tin-based solutions which raise environmental and health concerns, an issue of particular relevance in wearable electronics. In addition, activation, a pre-treatment process in electroless plating, utilizes increasingly costly noble metals, which poses economic limitations for large-scale implementation. Thus, there is a need for an alternative electroless plating process that mitigates health risks while improving scalability and cost-effectiveness.</p>

<p><strong>Innovation:</strong><br />
<br />
Researchers at UCLA have developed an electroless plating solution capable of forming metal thin films on chemically inert substrates without the use of traditional sensitization and activation techniques. This formulation enables copper deposition on PI and PET films without the need for toxic tin sensitization or noble metal activation reagents. This methodology significantly simplifies the production of polymer-metal thin-film composites and compresses the processing timeline, as functional films form within minutes. The system&rsquo;s wide applicability is driven by a facile salt metathesis protocol, which allows for the deposition of many metals using standard solutions. The system can accommodate most transition metal ions used in industrial thin films while maintaining conventional film formation characteristics. Furthermore, the system minimizes the deleterious surface wetting issues found in aqueous solutions, enabling uniform plating on hydrophobic plastics and glass. The technology provides precise control over surface morphology, ensuring that prolonged plating time leads to smooth and uniform surfaces. In conclusion, this methodology provides a precise and widely applicable framework that improves the production of polymer-metal thin-film composites by simplifying the process and improving scalability.</p>

<p><strong>Potential Applications:</strong><br />
<br />
●&nbsp;&nbsp; &nbsp;Flexible Electronics and Circuits<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;Wearable biosensors<br />
●&nbsp;&nbsp; &nbsp;EMI/RFI Shielding<br />
●&nbsp;&nbsp; &nbsp;Advanced Sensors<br />
●&nbsp;&nbsp; &nbsp;Microfluidics<br />
●&nbsp;&nbsp; &nbsp;Aerospace and defense&nbsp;<br />
●&nbsp;&nbsp; &nbsp;Automotive materials<br />
●&nbsp;&nbsp; &nbsp;Any application where thin layers of copper are desired</p>

<p><strong>Advantages:</strong><br />
<br />
●&nbsp;&nbsp; &nbsp;Simplified pre-treatment<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;Cost effectiveness<br />
●&nbsp;&nbsp; &nbsp;Non-Toxic Reagents<br />
●&nbsp;&nbsp; &nbsp;Rapid processing<br />
●&nbsp;&nbsp; &nbsp;Scalability<br />
●&nbsp;&nbsp; &nbsp;Controllable thickness of applied metal films</p>

<p><strong>Development-To-Date:</strong><br />
<br />
Compound developed; validation in progress.</p>

<p><strong>Related Papers:</strong><br />
<br />
●&nbsp; &nbsp; Nava, Matthew., et al. &ldquo;Metal&ndash;Ligand Cooperativity Enables Zero-Valent Metal Transfer.&rdquo; Chemical Science, vol. 16, 2025, pp. 3888&ndash;3894. Royal Society of Chemistry, https://doi.org/10.1039/D4SC07938H</p>

<p><strong>Reference: </strong><br />
<br />
UCLA Case No. 2026-211</p>

<p><strong>Lead Inventors: </strong><br />
<br />
Matthew Nava, Oliver Garcia<br />
&nbsp;</p>]]></description><pubDate>Tue, 14 Apr 2026 15:03:27 GMT</pubDate><author>marketing@tdg.ucla.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Electroless_Plating_Solution_for_Forming_Metal_Films_on_Inert_Substrates_(Case_No._2026-211)</guid><dataField:caseId>2026-211</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 15:04:01 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Matthew</dataField:firstName><dataField:lastName>Nava</dataField:lastName><dataField:title>ASST PROF-AY</dataField:title><dataField:department>CHEMISTRY AND BIOCHEMISTRY [0980]</dataField:department><dataField:emailAddress>mjnava@ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Oliver</dataField:firstName><dataField:lastName>Garcia</dataField:lastName><dataField:title>TEACHG ASST-GSHIP</dataField:title><dataField:department>CHEMISTRY AND BIOCHEMISTRY [0980]</dataField:department><dataField:emailAddress>oliveregarcia13@ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Ed</dataField:firstName><dataField:lastName>Beres</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>edward.beres@tdg.ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Materials| Materials > Composite Materials| Materials > Fabrication Technologies| Materials > Functional Materials| Materials > Metals| Materials > Nanotechnology]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Method for performing federated learning in non-convex problems</title><link>https://canberra-ip.technologypublisher.com/tech/Method_for_performing_federated_learning_in_non-convex_problems</link><description><![CDATA[<p ></p>

<p >​<img src="https://rutgers.technologypublisher.com/files/sites/image1948.png"  /></p>

<p >FeCA roadmap. 1st column: The centralized dataset distributed to clients. 2nd column: The k-means clustering results on different clients under non-IID data sample scenario, where black triangles and squares represent centroids. 3rd column: Eliminating one-fit-many centroids in Algorithm 2, indicated by hollow squares and triangles. 4th column: Centroids sent to the server. 5th column: Aggregation of received centroids on the server where red crosses represent recovered centroids.</p>

<p ></p>

<p ><br />
<strong>Invention Summary:</strong> </p>

<p ></p>

<p >FeCA, a one-shot federated clustering method, provides data privacy and enhanced performance by leveraging models trained locally on users&rsquo; devices. Traditional centralized machine learning approaches often face limitations due to siloed, private datasets that are limited in quantity and diversity.</p>

<p ></p>

<p >Rutgers researchers have developed a method that developed a one-shot federated learning (provides data privacy by having models trained locally on a user&rsquo;s device) for clustering (partitions a dataset into different groups based on the similarity of individual datapoints) by first performing standard clustering on the user&rsquo;s device, refining the model, and then aggregating the refined model with that from other users&rsquo; devices. There is also a framework to expand this technique to other non-convex machine learning problems, including neural networks, enabling models to capture more consistent and nuanced patterns across user datasets.</p>

<p >&nbsp;</p>

<p ></p>

<p ><strong> Market Applications: </strong></p>

<ul>
	<li ><em>General clustering problems </em></li>
	<li ><em>Natural Language Processing </em></li>
	<li ><em>Healthcare disease detection -disease subtype analysis</em></li>
	<li ><em>Recommendation engines </em></li>
	<li ><em>Customer classification </em></li>
	<li ><em>Anomaly detection</em></li>
</ul>

<p ><strong>Advantages:</strong></p>

<ul>
	<li ><em>Minimal communication overhead </em></li>
	<li ><em>Allow for heterogeneous data/model to accelerate convergence </em></li>
	<li ><em>Safeguarding user privacy</em></li>
</ul>

<p ><strong>Publications: </strong></p>

<div class="WordSection1">
<ul>
	<li >Xu, J., Chen, H. Y., Chao, W. L., &amp; Zhang, Y. (2024). Jigsaw game: Federated clustering.&nbsp;Transactions on Machine Learning Research,&nbsp;2024</li>
</ul>
</div>

<div >&nbsp;</div>

<p ><strong>Intellectual Property &amp; Development Status:&nbsp;</strong>Provisional application filed.<strong> </strong>Patent pending. Available for licensing and/or research collaboration.&nbsp;For any business development and other collaborative partnerships, contact:&nbsp; <a href="mailto:marketingbd@research.rutgers.edu"  target="_blank">marketingbd@research.rutgers.edu</a> </p>]]></description><pubDate>Tue, 14 Apr 2026 13:32:35 GMT</pubDate><author>christopher.perkins@rutgers.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Method_for_performing_federated_learning_in_non-convex_problems</guid><dataField:caseId>2025-069</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 10:22:32 GMT</dataField:lastUpdateDate><dataField:Image><![CDATA[</span></span></span></span></p>

<p style="margin-bottom:11px; text-align:center"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">​</span></span></span></span></span><img src="https://rutgers.technologypublisher.com/files/sites/image1948.png" style="display:block; margin-left:auto; margin-right:auto" /></p>

<p style="text-align:center"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><span style="font-size:8.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">FeCA roadmap. 1st column: The centralized dataset distributed to clients. 2nd column: The k-means clustering results on different clients under non-IID data sample scenario, where black triangles and squares represent centroids. 3rd column: Eliminating one-fit</span></span><span style="font-size:8.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">-</span></span><span style="font-size:8.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">many centroids in Algorithm 2, indicated by hollow squares and triangles. 4th column: Centroids sent to the server. 5th column: Aggregation of received centroids on the server where red crosses represent recovered centroids.</span></span></span></span></span></span></p>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Image><dataField:AlgoliaSummary><![CDATA[</span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">FeCA, a one-shot </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">federated </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">clustering method, provides data privacy and enhanced performance by leveraging models trained locally on users&rsquo; devices. Traditional</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"> centralized </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">machine learning approaches often face limitations due to siloed</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">,</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"> private datasets </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">that are limited</span></span> <span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">in </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">quantity and diversity.</span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:AlgoliaSummary><dataField:Left><![CDATA[<strong>Invention Summary:</strong> </span></span></span></span></p>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"></span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">FeCA, a one-shot </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">federated </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">clustering method, provides data privacy and enhanced performance by leveraging models trained locally on users&rsquo; devices. Traditional</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"> centralized </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">machine learning approaches often face limitations due to siloed</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">,</span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"> private datasets </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">that are limited</span></span> <span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">in </span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">quantity and diversity.</span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"></span></span></span></span></span></p>

<p style="text-align:justify"><span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Rutgers researchers have developed a method that developed a one-shot federated learning (provides data privacy by having models trained locally on a user&rsquo;s device) for clustering (partitions a dataset into different groups based on the similarity of individual datapoints) by first performing standard clustering on the user&rsquo;s device, refining the model, and then aggregating the refined model with that from other users&rsquo; devices. There is also a framework to expand this technique to other non-convex machine learning problems, including neural networks, enabling models to capture more consistent and nuanced patterns across user datasets.</span></span></span></span></span></p>

<p style="text-align:justify">&nbsp;</p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Left><dataField:Right><![CDATA[<strong> Market Applications: </strong></span></span></span></span></p>

<ul>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">General clustering problems </span></span></span></em></span></span></span></span></li>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">Natural Language Processing </span></span></span></em></span></span></span></span></li>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Healthcare disease detection -disease subtype analysis</span></span></em></span></span></span></span></li>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">Recommendation engines </span></span></span></em></span></span></span></span></li>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">Customer classification </span></span></span></em></span></span></span></span></li>
	<li style="margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="text-autospace:none"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">Anomaly detection</span></span></span></em></span></span></span></span></li>
</ul>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-family:&quot;Palatino Linotype&quot;,serif">Advantages:</span></strong></span></span></span></p>

<ul>
	<li style="text-align:justify; margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="tab-stops:145.5pt"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Minimal communication overhead </span></span></em></span></span></span></span></li>
	<li style="text-align:justify; margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="tab-stops:145.5pt"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Allow for heterogeneous data/model to accelerate convergence </span></span></em></span></span></span></span></li>
	<li style="text-align:justify; margin-left:8px"><span style="font-size:11pt"><span style="line-height:normal"><span style="tab-stops:145.5pt"><span style="font-family:Calibri,sans-serif"><em><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Safeguarding user privacy</span></span></em></span></span></span></span></li>
</ul>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-family:&quot;Palatino Linotype&quot;,serif">Publications: </span></strong></span></span></span></p>

<div class="WordSection1">
<ul>
	<li style="text-align:justify; margin-left:8px"><span style="page:WordSection1"><span style="font-size:11pt"><span style="line-height:normal"><span style="tab-stops:145.5pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:9.0pt"><span style="background-color:white"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:black">Xu, J., Chen, H. Y., Chao, W. L., &amp; Zhang, Y. (2024). Jigsaw game: Federated clustering.&nbsp;</span></span></span></span><span style="font-size:9.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Transactions on Machine Learning Research,&nbsp;2024</span></span></span></span></span></span></span></li>
</ul>
</div>

<div style="page-break-after:always"><span style="display:none">&nbsp;</span></div>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Intellectual Property &amp; Development Status:&nbsp;</span></span></strong><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Provisional application filed.<strong> </strong></span></span><span style="font-size:11.0pt"><span style="background-color:white"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:#242424">Patent pending. Available for licensing and/or research collaboration.&nbsp;For any business development and other collaborative partnerships, contact:&nbsp; </span></span></span></span><a href="mailto:marketingbd@research.rutgers.edu" style="color:#0563c1; text-decoration:underline" target="_blank"><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">marketingbd@research.rutgers.edu</span></span></a> <span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Right><dataField:inventorList><dataField:inventor><dataField:firstName>Yuqian</dataField:firstName><dataField:lastName>Zhang</dataField:lastName><dataField:title>ASST PROFESSOR ACD YR</dataField:title><dataField:department>School of Engineering</dataField:department><dataField:emailAddress>yqz.zhang@rutgers.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Wei-Lun</dataField:firstName><dataField:lastName>Chao</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>chao.209@osu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Jinxuan</dataField:firstName><dataField:lastName>Xu</dataField:lastName><dataField:title>Student</dataField:title><dataField:department></dataField:department><dataField:emailAddress>jx185@scarletmail.rutgers.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Wenjuan</dataField:firstName><dataField:lastName>Zhu</dataField:lastName><dataField:title>Licensing Manager</dataField:title><dataField:department>Innovation Ventures</dataField:department><dataField:emailAddress>wz284@research.rutgers.edu</dataField:emailAddress><dataField:phoneNumber>848-932-4058</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Artificial Intelligence & Machine Learning| Technology Classifications > Software & Algorithms]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title><![CDATA[Pharmacological Treatment for Sleep Disorders Improving Sleep Quality & Architecture]]></title><link>https://canberra-ip.technologypublisher.com/tech?title=Pharmacological_Treatment_for_Sleep_Disorders_Improving_Sleep_Quality_%2b_Architecture</link><description><![CDATA[<p>Targeting Heat Shock Factor 1 (HSF1) via gene therapy or using pharmacological compounds targeting HSF1 (e.g. geranylgeranylacetone or macrocyclic peptides) can increase sleep stability, promote deeper sleep, reduce sleep fragmentation, and improve recovery from sleep loss.<br />
Problem:<br />
Millions of people worldwide suffer from disrupted sleep, whether due to modern &quot;24/7&quot; lifestyles, stress, aging and menopause, or underlying health conditions. Yet current treatments largely sedate patients without actually improving the quality of sleep - they can disrupt normal sleep architecture and fail to promote the deep, restorative stages that the brain and body need. This matters because poor sleep is not merely an inconvenience but is closely linked to cognitive decline, neurodegenerative disease, and reduced productivity. There is thus a critical need for therapies that restore how sleep naturally works, rather than simply masking symptoms.<br />
Solution:<br />
Dr. Reddy and his team showed that HSF1 overexpression in mice enhanced exhibited longer, uninterrupted sleep bouts and fewer awakenings. When mice were exposed to sleep deprivation, the mice overexpressing HSF1 exhibited enhanced recovery sleep efficiency which implies that HSF1 activation could mitigate the negative consequences of sleep loss, a feature with potential translational applications for individuals experiencing sleep deprivation.<br />
Technology:<br />
GGA: Geranylgeranylacetone (GGA) is a drug that has been safely used in Japan since 1984 to treat stomach ulcers. It has also been found to be a powerful activator of HSF1. With decades of clinical use and no reported neurological side effects, GGA is a strong candidate for repurposing to activate HSF1 in humans to improve sleep and treat sleep disorders. In mouse studies, GGA produced the same sleep benefits seen with direct HSF1 overexpression, including more stable sleep patterns and improved recovery after sleep loss. GGA shows the same HSF1-driven effects in fruit fly and roundworm sleep models, confirming that this mechanism is deeply conserved across species.&nbsp;<br />
<br />
Macrocyclic peptides: Beyond GGA, the team is developing AI-designed macrocyclic peptides, ring-shaped molecules engineered to activate HSF1 with greater potency and precision. These macrocycles are Pareto-optimized, meaning multiple competing properties such as potency, selectivity, and safety are balanced simultaneously rather than trading one off against another. Using proprietary techniques, the designs target optimal ADME (absorption, distribution, metabolism, and excretion) and brain penetration in vivo.&nbsp;<br />
<br />
Genetic expression: For severe sleep disorders linked to Alzheimer&#39;s, Parkinson&#39;s, or traumatic brain injury, AAV-mediated HSF1 overexpression could provide a one-time genetic intervention, with mRNA delivery as an adaptable alternative.<br />
<br />
Together, these HSF1 activators open a broad market opportunity, from everyday sleep improvement for professionals, parents, and aging populations (e.g. menopausal women) to cognitive enhancement for executives, athletes, and students seeking maximum restoration from limited sleep.<br />
Advantages:<br />
</p>

<ul>
	<li>First-in-class mechanism</li>
	<li>Restoration of natural sleep architecture at the molecular level</li>
	<li>Mechanism conserved across species (mice, fruit flies, roundworms), increasing translational confidence</li>
	<li>Minimal side effects: HSF1 activation does not impair cognition, motor function, or induce next-day drowsiness</li>
	<li>Non-addictive mechanism of action, unlike benzodiazepines and related sedatives</li>
	<li>Does not suppress REM or other essential sleep stages, unlike many current sleep drugs</li>
	<li>Potentially accelerated path to market by utilizing clinically tested GGA</li>
	<li>GGA&rsquo;s well-established safety profile and no reported neurological side effects</li>
	<li>Compatible with existing therapies for full sleep restoration</li>
	<li>Increase in sleep stability and reduction of sleep fragmentation</li>
	<li>Support of deeper sleep and improved recovery from sleep loss</li>
	<li>Potential to reduce total sleep time needed by improving restorative efficiency</li>
	<li>Broad therapeutic reach: applicable across lifestyle, wellness, and neurodegenerative disease markets</li>
	<li>Platform extensibility: GGA insights inform next-generation macrocyclic peptides and gene therapy approaches</li>
</ul>

<p>Stage of Development:<br />
</p>

<ul>
	<li>Preclinical</li>
</ul>

<p><br />
<img alt="" src="https://upenn.technologypublisher.com/files/sites/25-11089_image01.jpg"  /><br />
<br />
Intellectual Property:<br />
</p>

<ul>
	<li>Provisional filed</li>
</ul>

<p>Desired Partnerships:<br />
</p>

<ul>
	<li>Co-development</li>
	<li>Licensing</li>
</ul>

<p>Docket # 25-11089</p>]]></description><pubDate>Tue, 14 Apr 2026 13:16:05 GMT</pubDate><author>lbricha@upenn.edu</author><guid>https://canberra-ip.technologypublisher.com/tech?title=Pharmacological_Treatment_for_Sleep_Disorders_Improving_Sleep_Quality_%2b_Architecture</guid><dataField:caseId>25-11089-TpNCS</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 13:37:49 GMT</dataField:lastUpdateDate><dataField:brief>Targeting Heat Shock Factor 1 (HSF1) via gene therapy or using pharmacological compounds targeting HSF1 (e.g. geranylgeranylacetone or macrocyclic peptides) can increase sleep stability, promote deeper sleep, reduce sleep fragmentation, and improve recovery from sleep loss.</dataField:brief><dataField:contentproblem>Problem:</dataField:contentproblem><dataField:problem><![CDATA[Millions of people worldwide suffer from disrupted sleep, whether due to modern &quot;24/7&quot; lifestyles, stress, aging and menopause, or underlying health conditions. Yet current treatments largely sedate patients without actually improving the quality of sleep - they can disrupt normal sleep architecture and fail to promote the deep, restorative stages that the brain and body need. This matters because poor sleep is not merely an inconvenience but is closely linked to cognitive decline, neurodegenerative disease, and reduced productivity. There is thus a critical need for therapies that restore how sleep naturally works, rather than simply masking symptoms.]]></dataField:problem><dataField:contentsolution>Solution:</dataField:contentsolution><dataField:solution>Dr. Reddy and his team showed that HSF1 overexpression in mice enhanced exhibited longer, uninterrupted sleep bouts and fewer awakenings. When mice were exposed to sleep deprivation, the mice overexpressing HSF1 exhibited enhanced recovery sleep efficiency which implies that HSF1 activation could mitigate the negative consequences of sleep loss, a feature with potential translational applications for individuals experiencing sleep deprivation.</dataField:solution><dataField:contenttechnology>Technology:</dataField:contenttechnology><dataField:technology><![CDATA[GGA: Geranylgeranylacetone (GGA) is a drug that has been safely used in Japan since 1984 to treat stomach ulcers. It has also been found to be a powerful activator of HSF1. With decades of clinical use and no reported neurological side effects, GGA is a strong candidate for repurposing to activate HSF1 in humans to improve sleep and treat sleep disorders. In mouse studies, GGA produced the same sleep benefits seen with direct HSF1 overexpression, including more stable sleep patterns and improved recovery after sleep loss. GGA shows the same HSF1-driven effects in fruit fly and roundworm sleep models, confirming that this mechanism is deeply conserved across species.&nbsp;<br />
<br />
Macrocyclic peptides: Beyond GGA, the team is developing AI-designed macrocyclic peptides, ring-shaped molecules engineered to activate HSF1 with greater potency and precision. These macrocycles are Pareto-optimized, meaning multiple competing properties such as potency, selectivity, and safety are balanced simultaneously rather than trading one off against another. Using proprietary techniques, the designs target optimal ADME (absorption, distribution, metabolism, and excretion) and brain penetration in vivo.&nbsp;<br />
<br />
Genetic expression: For severe sleep disorders linked to Alzheimer&#39;s, Parkinson&#39;s, or traumatic brain injury, AAV-mediated HSF1 overexpression could provide a one-time genetic intervention, with mRNA delivery as an adaptable alternative.<br />
<br />
Together, these HSF1 activators open a broad market opportunity, from everyday sleep improvement for professionals, parents, and aging populations (e.g. menopausal women) to cognitive enhancement for executives, athletes, and students seeking maximum restoration from limited sleep.]]></dataField:technology><dataField:contentadvantages>Advantages:</dataField:contentadvantages><dataField:advantages><![CDATA[</p>

<ul>
	<li>First-in-class mechanism</li>
	<li>Restoration of natural sleep architecture at the molecular level</li>
	<li>Mechanism conserved across species (mice, fruit flies, roundworms), increasing translational confidence</li>
	<li>Minimal side effects: HSF1 activation does not impair cognition, motor function, or induce next-day drowsiness</li>
	<li>Non-addictive mechanism of action, unlike benzodiazepines and related sedatives</li>
	<li>Does not suppress REM or other essential sleep stages, unlike many current sleep drugs</li>
	<li>Potentially accelerated path to market by utilizing clinically tested GGA</li>
	<li>GGA&rsquo;s well-established safety profile and no reported neurological side effects</li>
	<li>Compatible with existing therapies for full sleep restoration</li>
	<li>Increase in sleep stability and reduction of sleep fragmentation</li>
	<li>Support of deeper sleep and improved recovery from sleep loss</li>
	<li>Potential to reduce total sleep time needed by improving restorative efficiency</li>
	<li>Broad therapeutic reach: applicable across lifestyle, wellness, and neurodegenerative disease markets</li>
	<li>Platform extensibility: GGA insights inform next-generation macrocyclic peptides and gene therapy approaches]]></dataField:advantages><dataField:contentstage>Stage of Development:</dataField:contentstage><dataField:stage><![CDATA[</p>

<ul>
	<li>Preclinical]]></dataField:stage><dataField:image><![CDATA[<br />
<img alt="" src="https://upenn.technologypublisher.com/files/sites/25-11089_image01.jpg" style="height:500px; width:725px" /><br />]]></dataField:image><dataField:contentip>Intellectual Property:</dataField:contentip><dataField:ip><![CDATA[</p>

<ul>
	<li>Provisional filed]]></dataField:ip><dataField:contentpartnerships>Desired Partnerships:</dataField:contentpartnerships><dataField:partnerships><![CDATA[</p>

<ul>
	<li>Co-development</li>
	<li>Licensing]]></dataField:partnerships><dataField:docket>Docket # 25-11089</dataField:docket><dataField:inventorList><dataField:inventor><dataField:firstName>Akhilesh Basi</dataField:firstName><dataField:lastName>Reddy</dataField:lastName><dataField:title>Associate Professor</dataField:title><dataField:department>SOM-Pharmacology</dataField:department><dataField:emailAddress>AKHILESH.REDDY@PENNMEDICINE.UPENN.EDU</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Shintaro</dataField:firstName><dataField:lastName>Yamazaki</dataField:lastName><dataField:title>Postdoctoral Researcher</dataField:title><dataField:department>SOM-Pharmacology</dataField:department><dataField:emailAddress>shintaro.yamazaki@pennmedicine.upenn.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Aging, Drug Target, Gene Therapy, Neurodegenerative Diseases, Protein/Peptide (Non-Antibody), Small Molecule, Women's Health, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Linara</dataField:firstName><dataField:lastName>Axanova</dataField:lastName><dataField:title>Interim Director, PSOM Licensing Group</dataField:title><dataField:department>Penn Center for Innovation</dataField:department><dataField:emailAddress>axanova@upenn.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Simulation-Based Wildfire Spread Modeling Tool for Community-Scale Risk Assessment (SWUIFT)</title><link>https://canberra-ip.technologypublisher.com/tech/Simulation-Based_Wildfire_Spread_Modeling_Tool_for_Community-Scale_Risk_Assessment_(SWUIFT)</link><description><![CDATA[<p> This technology enables community-scale wildfire risk assessment using a simulation-based model that predicts fire spread and damage within the wildland-urban interface, supporting proactive mitigation and emergency planning.</p>

<p>&nbsp;</p>

<p><strong>BACKGROUND:</strong></p>

<p> Communities and infrastructure owners currently lack effective tools to estimate wildfire spread and resulting damage at the community scale, particularly within the wildland-urban interface (WUI). Existing wildfire models often focus on large-scale fire behavior or wildland environments andD do not adequately capture fire propagation through built environments. This limitation constrains the ability of planners, utilities, and emergency responders to conduct proactive mitigation, scenario planning, and real-time decision-making. There is a critical need for modeling tools that can simulate wildfire behavior within communities to better inform risk assessment and resilience strategies.</p>

<p>&nbsp;</p>

<p><strong>TECHNOLOGY OVERVIEW:</strong></p>

<p> This University at Buffalo technology introduces SWUIFT, a simulation-based wildfire spread modeling tool designed to capture fire propagation within communities. The model represents both urban fuels (e.g., buildings and infrastructure) and vegetation within a unified computational framework, enabling estimation of fire arrival times, spread dynamics, and potential damage. SWUIFT incorporates efficient computational methods and accounts for uncertainties in environmental and structural conditions, allowing for robust scenario-based analysis. The platform supports detailed modeling of fire behavior as it transitions from wildland areas into densely built environments, providing actionable insights for community-level wildfire risk assessment.</p>

<p>&nbsp;</p>

<p>https://buffalo.technologypublisher.com/files/sites/7768_in-part_image.jpg</p>

<p>SE Viera Photo, https://stock.adobe.com/uk/images/359013282, stock.adobe.com</p>

<p>&nbsp;</p>

<p><strong>ADVANTAGES:</strong> </p>

<p> This technology provides one of the first explicit simulation frameworks for modeling wildfire spread within communities, addressing a key gap in existing wildfire modeling approaches. By integrating both urban and wildland fuels, it offers a more realistic representation of fire behavior in the wildland-urban interface. The model demonstrates efficient computational performance, enabling practical use in planning and decision-support contexts. It also incorporates uncertainty analysis, allowing users to evaluate a range of possible fire scenarios and outcomes, improving risk-informed decision-making.</p>

<p></p>

<p>&nbsp;</p>

<p><strong>APPLICATIONS:</strong></p>

<p> This technology can be applied in decision-support software for utilities, municipalities, and emergency management agencies to support wildfire risk assessment, mitigation planning, and emergency preparedness. It is suitable for scenario-based planning tools, infrastructure resilience analysis, and post-fire damage assessment. The platform can also be integrated into broader geospatial and climate risk modeling systems, as well as used in research and policy development related to wildfire management and community resilience.</p>

<p>&nbsp;</p>

<p><strong>INTELLECTUAL PROPERTY SUMMARY:</strong></p>

<p>&nbsp;</p>

<p>Provisional patent application 63/965,917 filed January 22, 2026.</p>

<p>&nbsp;</p>

<p><strong>STAGE OF DEVELOPMENT:</strong></p>

<p><a href="https://en.wikipedia.org/wiki/Technology_readiness_level"  target="_blank">Technology Readiness Level 8 (TRL 8)</a></p>

<p>&nbsp;</p>

<p><strong>LICENSING STATUS</strong>:</p>

<p>Available for licensing or collaboration</p>

<p>&nbsp;</p>

<p><strong>ADDITIONAL INFORMATION:</strong></p>

<p></p>

<p><img src="https://buffalo.technologypublisher.com/files/sites/image1947.png"  /></p>

<p>&nbsp;</p>

<p></p>]]></description><pubDate>Tue, 14 Apr 2026 11:06:20 GMT</pubDate><author>techtransfer@buffalo.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Simulation-Based_Wildfire_Spread_Modeling_Tool_for_Community-Scale_Risk_Assessment_(SWUIFT)</guid><dataField:caseId>030-7768</dataField:caseId><dataField:lastUpdateDate>Wed, 15 Apr 2026 08:46:15 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary><![CDATA[</span> This technology enables community-scale wildfire risk assessment using a simulation-based model that predicts fire spread and damage within the wildland-urban interface, supporting proactive mitigation and emergency planning.<span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:AlgoliaSummary><dataField:HDBackground><![CDATA[<strong>BACKGROUND:</strong></span><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:HDBackground><dataField:Background><![CDATA[</span> Communities and infrastructure owners currently lack effective tools to estimate wildfire spread and resulting damage at the community scale, particularly within the wildland-urban interface (WUI). Existing wildfire models often focus on large-scale fire behavior or wildland environments andD do not adequately capture fire propagation through built environments. This limitation constrains the ability of planners, utilities, and emergency responders to conduct proactive mitigation, scenario planning, and real-time decision-making. There is a critical need for modeling tools that can simulate wildfire behavior within communities to better inform risk assessment and resilience strategies.<span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:Background><dataField:HDTechnology><![CDATA[<strong>TECHNOLOGY OVERVIEW:</strong></span><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:HDTechnology><dataField:Technology><![CDATA[</span> This University at Buffalo technology introduces SWUIFT, a simulation-based wildfire spread modeling tool designed to capture fire propagation within communities. The model represents both urban fuels (e.g., buildings and infrastructure) and vegetation within a unified computational framework, enabling estimation of fire arrival times, spread dynamics, and potential damage. SWUIFT incorporates efficient computational methods and accounts for uncertainties in environmental and structural conditions, allowing for robust scenario-based analysis. The platform supports detailed modeling of fire behavior as it transitions from wildland areas into densely built environments, providing actionable insights for community-level wildfire risk assessment.<span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:Technology><dataField:Picture>https://buffalo.technologypublisher.com/files/sites/7768_in-part_image.jpg</dataField:Picture><dataField:PictureRef><![CDATA[</span></span></span></span>SE Viera Photo, https://stock.adobe.com/uk/images/359013282, stock.adobe.com<span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:PictureRef><dataField:HDAdvantages><![CDATA[<strong>ADVANTAGES:</strong>]]></dataField:HDAdvantages><dataField:Advantages><![CDATA[</span> This technology provides one of the first explicit simulation frameworks for modeling wildfire spread within communities, addressing a key gap in existing wildfire modeling approaches. By integrating both urban and wildland fuels, it offers a more realistic representation of fire behavior in the wildland-urban interface. The model demonstrates efficient computational performance, enabling practical use in planning and decision-support contexts. It also incorporates uncertainty analysis, allowing users to evaluate a range of possible fire scenarios and outcomes, improving risk-informed decision-making.</span></span></span></p>

<p><span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:Advantages><dataField:HDApplication><![CDATA[<strong>APPLICATIONS:</strong>]]></dataField:HDApplication><dataField:Application><![CDATA[</span> This technology can be applied in decision-support software for utilities, municipalities, and emergency management agencies to support wildfire risk assessment, mitigation planning, and emergency preparedness. It is suitable for scenario-based planning tools, infrastructure resilience analysis, and post-fire damage assessment. The platform can also be integrated into broader geospatial and climate risk modeling systems, as well as used in research and policy development related to wildfire management and community resilience.<span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:Application><dataField:HDPatentStatus><![CDATA[<strong>INTELLECTUAL PROPERTY SUMMARY:</strong>]]></dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[</span>Provisional patent application 63/965,917 filed January 22, 2026.<span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:PatentStatus><dataField:HDStageOfDevelopment><![CDATA[<strong>STAGE OF DEVELOPMENT:</strong>]]></dataField:HDStageOfDevelopment><dataField:StageOfDevelopment><![CDATA[</span><span style="font-family:&quot;Times New Roman&quot;,serif"><a href="https://en.wikipedia.org/wiki/Technology_readiness_level" style="color:#0563c1; text-decoration:underline" target="_blank">Technology Readiness Level 8 (TRL 8)</a></span><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:StageOfDevelopment><dataField:HDLicensingStatus><![CDATA[<strong>LICENSING STATUS</strong>:]]></dataField:HDLicensingStatus><dataField:LicensingStatus><![CDATA[</span><span style="font-family:Calibri, sans-serif">Available for licensing or collaboration</span><span style="font-family:Arial,sans-serif">]]></dataField:LicensingStatus><dataField:HDAdditionalInfo><![CDATA[<strong>ADDITIONAL INFORMATION:</strong>]]></dataField:HDAdditionalInfo><dataField:AdditionalInfo><![CDATA[</span></span></span></span></p>

<p><img src="https://buffalo.technologypublisher.com/files/sites/image1947.png" style="height:629px; width:722px" /></p>

<p>&nbsp;</p>

<p><span style="font-size:11pt"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-family:&quot;Arial&quot;,sans-serif">]]></dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Negar</dataField:firstName><dataField:lastName>Elhami-Khorasani</dataField:lastName><dataField:title>Associate Professor</dataField:title><dataField:department><![CDATA[Civil, Structural & Environmental Engineering]]></dataField:department><dataField:emailAddress>negarkho@buffalo.edu</dataField:emailAddress><dataField:phoneNumber>716-645-3019</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Fernando</dataField:firstName><dataField:lastName>Szasdi-Bardales</dataField:lastName><dataField:title>Former UB PhD student</dataField:title><dataField:department><![CDATA[Civil, Structural & Environmental Engineering]]></dataField:department><dataField:emailAddress>szasdi-bardales.research@outlook.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Nima</dataField:firstName><dataField:lastName>Masoudvaziri</dataField:lastName><dataField:title>Former UB PhD student</dataField:title><dataField:department><![CDATA[Civil, Structural & Environmental Engineering]]></dataField:department><dataField:emailAddress>nimamasoudvaziri@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Technologies, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Evan</dataField:firstName><dataField:lastName>Witmer</dataField:lastName><dataField:title>Licensing Manager</dataField:title><dataField:department>Technology Transfer</dataField:department><dataField:emailAddress>evanwitm@buffalo.edu</dataField:emailAddress><dataField:phoneNumber>(716) 645-8181</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > University at Buffalo| Technology Classifications > Agriculture| Technology Classifications > Environment]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Nano-therapeutics Targeting Cholesterol Efflux Transporter in Macrophages for Cancer Immunotherapy</title><link>https://canberra-ip.technologypublisher.com/tech/Nano-therapeutics_Targeting_Cholesterol_Efflux_Transporter_in_Macrophages_for_Cancer_Immunotherapy</link><description><![CDATA[<p ><strong>NU 2025-160</strong><br />
<br />
<strong>INVENTORS</strong></p>

<ul>
	<li >Jason Miska*

	<ul>
		<li >Feinberg School of Medicine, Department of Neurological Surgery</li>
	</ul>
	</li>
	<li >Peng Zhang*
	<ul>
		<li >Feinberg School of Medicine, Department of Neurological Surgery</li>
	</ul>
	</li>
</ul>

<p ><br />
<strong>SHORT DESCRIPTION</strong><br />
Novel nanoparticle technology that modulates macrophage cholesterol metabolism to boost anti-tumor immunity in GBM.<br />
<br />
<strong>BACKGROUND</strong><br />
Glioblastoma (GBM) is the most aggressive primary brain tumor in adults, and&nbsp;effective treatment options are severely limited. Current therapies deliver only modest survival benefits largely due to a profoundly immunosuppressive tumor microenvironment&nbsp;characterized by the predominance of tumor-associated macrophages (TAMs), which are a key driver of immunosuppression and therapy resistance.&nbsp;Cholesterol acts as a critical regulator of macrophage function, with high intracellular cholesterol levels triggering polarization toward a pro-inflammatory phenotype, while lower levels or efficient cholesterol efflux can promote polarization toward an anti-inflammatory phenotype. Moreover, GBM cells rely heavily on cholesterol, reprogramming their metabolism to import and accumulate massive amounts of it to support rapid cell membrane synthesis, proliferation, and survival. Modulating cholesterol efflux in TAMs&nbsp; has been shown to reprogram TAMs to achieve enhanced antigen presentation, increased production of pro-inflammatory cytokines, and significantly improved therapeutic outcomes in glioma models, especially when combined with radiation therapy and/or anti-PD-1 therapy. Therefore, targeting cholesterol efflux in TAMs has the potential to enhance anti-tumor immunity while simultaneously starving the tumor of essential nutrients, and represents a novel and promising approach in the treatment of GBM that is desperately needed.&nbsp;</p>

<p ><br />
<strong>ABSTRACT</strong><br />
<img alt="Kaplan-Meier survival curves for various experiments performed. A. Survival of CT-2A-bearing C57 mice treated with RT+ LNP. *** p&lt;0.001(Log-rank test). B. LNP target inhibition synergizes with anti-PD1 therapy. C. LNP target inhibition synergizes with radiation therapy in glioma model." src="https://nulive.technologypublisher.com/files/sites/2025-160.jpg"  />Northwestern researchers have developed a nanoparticle-based therapeutic strategy designed to inhibit cholesterol efflux in TAMs. This approach directs lipid nanoparticles to target these macrophages and inhibit their cholesterol efflux, leading to cholesterol accumulation and a switch toward a pro-inflammatory phenotype. In preclinical GBM models, this treatment reprogrammed TAMs and enhanced T cell-mediated anti-tumor responses, resulting in enhanced survival. This work establishes a new immunometabolic strategy with strong translational potential in overcoming GBM therapy resistance and delivering improved clinical outcomes.<br />
<br />
<strong>DEVELOPMENT STAGE</strong><br />
TRL-5 Prototype Validated in Relevant Environment: The therapy has demonstrated efficacy in preclinical GBM models, confirming key functions in a relevant in vivo setting.<br />
<br />
<strong>APPLICATIONS</strong></p>

<ul>
	<li >Glioblastoma treatment: Enhances anti-tumor immunity in aggressive brain tumors.</li>
	<li >Targeted inhibition: Inhibits key cholesterol transporters in macrophages.</li>
	<li >Cancer immunotherapy: Reprograms immunosuppressive tumor environments</li>
</ul>

<p ><strong>ADVANTAGES</strong></p>

<ul>
	<li >Novel target&nbsp;altering immunometabolism.</li>
	<li >Targeted delivery: Leverages functionalized lipid nanoparticles for precision therapy.</li>
	<li >Enhances immune response: Reprograms TAMs to a pro-inflammatory phenotype.</li>
	<li >Dual therapeutic effect: Reduces tumor support by inhibiting&nbsp;cholesterol efflux that fuels tumor cell survival.</li>
	<li >Improved survival: Shows strong efficacy in preclinical GBM models.</li>
	<li >Synergy with other therapeutic&nbsp;modalities: Improved outcomes when combined with radiation and/or immunotherapy</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<ul>
	<li >N/A</li>
</ul>

<p ><strong>IP STATUS</strong><br />
US Patent pending (63/956,990).<br />
<br />
<strong>CATEGORY/INDUSTRY PIPELINE</strong><br />
<img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2025-160.png"  />Therapeutics<br />
<br />
<strong>KEYWORDS</strong><br />
Cancer, oncology, nanotherapeutics, cholesterol efflux, macrophages, TAMs, glioblastoma, GBM, immunometabolism, immunotherapy, immune reprogramming, immunomodulation, lipid nanoparticles, LNP,&nbsp; targeted therapeutic</p>]]></description><pubDate>Tue, 14 Apr 2026 10:15:32 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Nano-therapeutics_Targeting_Cholesterol_Efflux_Transporter_in_Macrophages_for_Cancer_Immunotherapy</guid><dataField:caseId>2025-160</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:34:13 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Adjunct therapy, Brain cancer, Cancer/Oncology, CNS - Central Nervous System, Drug delivery, Immunotherapy, Nanoparticle, Neurologic disease, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>SEC61 Complex as a Novel Therapeutic Target to Enhance Immunotherapy Response in Glioblastoma</title><link>https://canberra-ip.technologypublisher.com/tech/SEC61_Complex_as_a_Novel_Therapeutic_Target_to_Enhance_Immunotherapy_Response_in_Glioblastoma</link><description><![CDATA[<div ><strong>NU 2023-011</strong><br />
<br />
<strong>INVENTORS</strong>
<ul>
	<li>Irina Balyasnikova*
	<ul>
		<li>Northwestern University Feinberg School of Medicine, Department of Neurological Surgery</li>
	</ul>
	</li>
	<li>Joseph Duffy</li>
</ul>
 <strong>SHORT DESCRIPTION</strong><br />
A targeted therapeutic approach that inhibits the SEC61 complex to enhance responses to immunotherapy in glioblastoma.<br />
<br />
<strong>BACKGROUND</strong><br />
<img alt=" Knockout of SEC61G sensitizes glioma cells to T-cell mediated killing. A. Cr51 release assay revealed a several-fold increase in cytotoxicity in response to targeted T-cell therapy in U87-SEC61G.KO compared to U87-NTC. B. Treatment of N10 and C. U87 glioma cells with SEC61 inhibitor A317 enhances responses to cytotoxic T cells in-co-culture assay." src="https://nulive.technologypublisher.com/files/sites/2023-011.jpg"  />Glioblastoma (GBM) is the most aggressive primary brain tumor in adults, and effective treatment options are severely limited. Current therapies, including surgery, radiation, and temozolomide, deliver only modest survival benefits largely due to a profoundly immunosuppressive tumor microenvironment. Moreover, while immunotherapy has delivered promising results with other types of cancer, it has not yet delivered clinical benefits for GBM due to tumor resistance. There is a pressing need for improved treatment methods that can overcome these barriers.<br />
<br />
<strong>ABSTRACT</strong><br />
Northwestern researchers have conducted an unbiased, genome-wide CRISPR knockout screen to identify genes that contribute to immunotherapeutic resistance in glioblastoma in the context of bispecific T-cell engager (BiTE) therapy. They found that inactivating SEC61G in vitro in glioma cell lines increases T-cell mediated cytotoxicity and upregulates MAPK pathway activation. Additionally, treatment of N10 and U87 glioma cells with SEC61 inhibitor enhances responses to cytotoxic T cells in co-culture assays. Furthermore, transcriptomic analysis confirmed that SEC61G is overexpressed and genomically amplified in a substantial portion of GBM patient samples. These findings indicate that targeting the SEC61 complex can enhance the efficacy of immunotherapy for glioblastoma.<br />
<br />
<strong>DEVELOPMENT STAGE</strong><br />
TRL-3 &ndash; Experimental Proof-of-Concept: Key functions have been validated in vitro using CRISPR knockout models in glioma cell lines to enhance T-cell therapy response.<br />
<br />
<strong>APPLICATIONS</strong>

<ul>
	<li>Improved immunotherapy for glioblastoma: Enhances patient response to targeted T-cell therapy.</li>
	<li>Gene-targeted therapy: Facilitates combination approaches with MAPK inhibitors.</li>
	<li>Personalized treatment strategies: Enables tailored interventions based on tumor gene expression.</li>
</ul>
 <strong>ADVANTAGES</strong>

<ul>
	<li>Enhances immunotherapy response: Boosts T-cell efficacy by modulating MAPK pathway activity.</li>
	<li>Overcomes tumor resistance: Disrupts a key component in GBM resistance mechanisms.</li>
	<li>Enables combinatorial treatment: Compatible with existing immunotherapeutic and targeted regimens.</li>
	<li>Validated approach: Demonstrated proof-of-concept with CRISPR knockout experiments.</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<p ><strong>IP STATUS</strong><br />
US Patent Pending (<a href="https://patents.google.com/patent/US20250099449A1/en?oq=+18%2f776%2c064" target="_blank">18/776,064</a>)<br />
<br />
<strong>CATEGORY/INDUSTRY PIPELINE</strong><br />
<img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2023-011.png"  />Therapeutics; Biomarkers &amp; Biomedical Research Tools<br />
<br />
<strong>KEYWORDS</strong><br />
GBM, Immunotherapy, SEC61 complex, MAPK, T-cell therapy, glioblastoma, cancer, oncology, resistance</p>
</div>

<p >&nbsp;</p>]]></description><pubDate>Tue, 14 Apr 2026 10:13:21 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/SEC61_Complex_as_a_Novel_Therapeutic_Target_to_Enhance_Immunotherapy_Response_in_Glioblastoma</guid><dataField:caseId>2023-011</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:31:20 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Brain cancer, Cancer/Oncology, Immunotherapy, Targeted therapy, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Anti-TYRP1 Bi-specific T cell Engager for Treatment of TYRP1-expressing melanoma</title><link>https://canberra-ip.technologypublisher.com/tech/Anti-TYRP1_Bi-specific_T_cell_Engager_for_Treatment_of_TYRP1-expressing_melanoma</link><description><![CDATA[<p ><strong>NU 2022-123</strong><br />
<br />
<strong>INVENTORS</strong></p>

<ul>
	<li>Irina Balyasnikova (Feinberg School of Medicine, Department of Neurological Surgery)*</li>
	<li>Isabelle Le Poole (Feinberg School of Medicine, Department of Dermatology)*</li>
</ul>

<p ><strong>SHORT DESCRIPTION</strong><br />
A bispecific T cell engager that targets CD3+ T cells and TYRP1-expressing melanoma cells.<br />
<img alt="Fold-change in tumor size in mice following subcutaneous injection of 888 A2 melanoma cells and treatment with a combination of the TYRP1 BTE and T cells or left untreated. Change in tumor size is shown from the onset of treatment, and the arrow indicates the repeat treatment date. TYRP1 BTE promotes T cell-mediated tumor growth suppression in vivo. " src="https://nulive.technologypublisher.com/files/sites/2022-1231.jpg"  /><br />
<strong>BACKGROUND</strong><br />
Melanoma is the deadliest form of skin cancer with an estimated 105,000 new cases and around 8,430 deaths expected in the United States in 2025. It is a UV-promoted form of skin cancer that readily metastasizes, and in patients in which metastasis has occurred, the survival rate is only 65% when the disease has spread to lymph nodes and 25% when distant spread has occurred. Current treatments for melanoma face high costs, poor specificity, limited effectiveness, and significant side effects; therefore, there is a clear unmet need for improved methods to target melanoma while minimizing adverse side effects.&nbsp; Melanoma is commonly infiltrated by T cells, a phenomenon known as a &ldquo;hot tumor&quot; which refers to cancer that has already triggered a strong immune response, has been infiltrated by immune cells like T cells, and is likely to respond well to immunotherapy. Bispecific T cell engagers (BiTEs) are a new type of immunotherapy which, when a tumor-specific cell surface antigen can be identified, can brings a patient&#39;s T-cells close to the cancer cells and activate the T-cells to kill the cancer. Tyrosinase-related protein 1 (TYRP1) is the most abundant protein expressed by melanocytic cells, and in melanoma tumor cells, the protein was recently shown to be partially trafficked to the cell surface. A novel therapeutic approach that exploits these characteristics of melanoma could address this unmet need and significantly improve clinical outcomes for patients.<br />
<br />
<strong>ABSTRACT</strong><br />
Northwestern researchers have developed a BiTE designed to target CD3&epsilon; expressed on the surface of T cells and TYRP1 expressed on the surface of melanoma cells. This innovative approach has been shown to trigger potent cytotoxic responses against melanoma cells with minimal damage to healthy tissues in vitro and in vivo evaluation in preclinical models have demonstrated its ability to mediate effective tumor cell killing. This therapeutic modality supports a simpler streamlined manufacturing process for an off-the-shelf product.</p>

<p ><br />
<strong>DEVELOPMENT STAGE</strong><br />
Early Preclinical - In Vivo PoC Data Available.<br />
<br />
<strong>APPLICATIONS</strong></p>

<ul>
	<li>Immunotherapy for melanoma: Applicable to both cutaneous and metastatic melanoma, including brain metastases.</li>
</ul>

<p ><strong>ADVANTAGES</strong></p>

<ul>
	<li>Improved specificity and safety: Minimizes potential side effects through targeted action.</li>
	<li>Overcomes immune evasion: Activates T cells independent of traditional activation pathways.</li>
	<li>Potent immune response: Induces strong cytotoxicity against melanoma cells, including bystander killing.</li>
	<li>Fast manufacturing: Simplifies production with an off-the-shelf format for rapid deployment.</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<p ><strong>IP STATUS</strong><br />
US patent pending (<a href="https://patents.google.com/patent/US20260049156A1/en?oq=US-2026-0049156-A1" target="_blank">19/103,495</a>).<br />
<br />
<strong>CATEGORY/INDUSTRY PIPELINE</strong><br />
<img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2022-123.png"  />Therapeutics<br />
<br />
<strong>KEYWORDS</strong><br />
Therapeutics, cancer, oncology, melanoma, immunotherapy, bispecific T cell engager, TYRP1, CD3, targeted therapy, off-the-shelf, biologic</p>]]></description><pubDate>Tue, 14 Apr 2026 10:10:19 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Anti-TYRP1_Bi-specific_T_cell_Engager_for_Treatment_of_TYRP1-expressing_melanoma</guid><dataField:caseId>2022-123</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:29:41 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Biologic, Cancer/Oncology, Immunotherapy, Melanoma, Targeted therapy, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>JNK Inhibitors Targeting Bergmann Glia Inflammation to Mitigate Spinocerebellar Ataxia and Other Neurodegenerative Disorders</title><link>https://canberra-ip.technologypublisher.com/tech/JNK_Inhibitors_Targeting_Bergmann_Glia_Inflammation_to_Mitigate_Spinocerebellar_Ataxia_and_Other_Neurodegenerative_Disorders</link><description><![CDATA[<p ><strong>NU2021-060</strong><br />
<br />
<strong>SHORT DESCRIPTION</strong> </p>

<p >Novel therapeutic strategy targeting Bergmann glia inflammation using JNK inhibition for treatment of spinocerebellar ataxia type 1 (SCA1) and other neurodegenerative disorders.<br />
<br />
<strong>INVENTORS</strong></p>


	
		
			<strong>INVENTORS</strong>

			<ul>
				<li>Puneet Opal*

				<ul>
					<li>Northwestern University Feinberg School of Medicine, Professor of Neurology</li>
				</ul>
				</li>
				<li>Chandrakanth Edamakanti</li>
			</ul>
			 <em>* Principal Investigator</em>
			
			<p ><strong>NU Tech ID&nbsp;&nbsp;</strong>NU 2021-060</p>

			<p ><strong>IP STATUS</strong></p>

			<p >US Patent Issued (<a href="https://patents.google.com/patent/US12414981B2/en?oq=US12414981B2" target="_blank">12,414,981</a>)</p>

			<p ><strong>DEVELOPMENT STAGE</strong></p>

			<p >TRL-3 Experimental Proof-of-Concept: Animal model studies reduced inflammation and improved motor function.</p>
			
		
	


<p ><br />
<strong>BACKGROUND</strong> </p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/2021060.png"  />Spinocerebellar ataxia type 1 (SCA1) is a rare and debilitating adult‑onset neurodegenerative disorder that causes progressive cerebellar and brainstem dysfunction leading to progressive loss of motor coordination, severe disability, and premature death. Current treatment options are limited and focus mainly on symptom management and supportive approaches like physiotherapy and occupational and speech therapy. The high cost and low efficacy of available treatments highlight a critical need for novel therapeutic approaches that address underlying neuroinflammatory mechanisms.<br />
<br />
<strong>ABSTRACT</strong></p>

<p >Northwestern researchers have&nbsp; developed a JNK inhibitor strategy to reduce neuroinflammation by targeting Bergmann glia in SCA1. Researchers observed a unique JNK-dependent c-Jun phosphorylation in Bergmann glia using human SCA autopsy samples. In an SCA1 mouse model, JNK inhibition decreased this inflammatory marker and led to significant improvements in both pathology and behavior. The results suggest that blocking the JNK pathway addresses a key contributor to neurodegeneration in SCA1 and potentially in other ataxic <img alt="Treatment of SCA1 mice with JNK inhibitor ameliorates the motor coordination impairment. " src="https://nulive.technologypublisher.com/files/sites/2021-060.png"  />syndromes.<br />
<br />
<strong>APPLICATIONS</strong></p>

<ul>
	<li>Therapeutic intervention for spinocerebellar ataxia: Offers a targeted treatment for SCA1 patients.</li>
	<li>Neuroinflammation reduction: Addresses inflammation in Bergmann glia across various neurodegenerative disorders.</li>
	<li>Preclinical research tool: Supports studies on JNK pathway modulation in animal models.</li>
	<li>Combination therapy potential: Can be paired with existing treatments to enhance clinical outcomes.</li>
</ul>

<p ><strong>ADVANTAGES</strong></p>

<ul>
	<li>Targets a specific inflammatory pathway: Focuses on the JNK-dependent phosphorylation in Bergmann glia.</li>
	<li>Improves pathological and behavioral outcomes: Validated in an SCA1 mouse model.</li>
	<li>Fills an unmet clinical need: Provides a novel approach where current therapies are limited.</li>
	<li>Potential for broader application: May benefit other ataxic syndromes with similar neuroinflammatory profiles.</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<ul>
	<li>Puneet Opal et al., <a href="https://link.springer.com/article/10.1186/s12974-023-02801-1" target="_blank">Reactive Bergmann glia play a central role in spinocerebellar ataxia inflammation via the JNK pathway</a>, J Neuroinflammation. May 26, 2023.</li>
</ul>

<p ><strong>CATEGORY/INDUSTRY PIPELINE</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2021-060.png"  />Therapeutics</p>

<p ><strong>KEYWORDS</strong></p>

<p >JNK inhibitor, neuroinflammation, spinocerebellar ataxia, SCA1, Bergmann glia, neurodegeneration, therapeutic, small molecule, neurodegenerative disease, CNS, rare disease</p>]]></description><pubDate>Tue, 14 Apr 2026 10:05:19 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/JNK_Inhibitors_Targeting_Bergmann_Glia_Inflammation_to_Mitigate_Spinocerebellar_Ataxia_and_Other_Neurodegenerative_Disorders</guid><dataField:caseId>2021-060</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:23:02 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Bergmann glia inflammation, Neurodegenerative disease, Neuroinflammation, Neurologic disease, Neurology, Rare diseases, SCA - Spinocerebellar ataxia, Small molecule, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Synthetic Receptors for IL-23</title><link>https://canberra-ip.technologypublisher.com/tech/Synthetic_Receptors_for_IL-23</link><description><![CDATA[<p ><strong>NU 2024-093</strong></p>

<p ><strong>SHORT DESCRIPTION</strong></p>

<p >Synthetic IL-23 receptors for cell engineering to enable real-time sensing and drive precise autoimmune and cancer immunotherapy interventions.</p>


	
		
			<strong>INVENTORS</strong>

			<ul>
				<li>Joshua Leonard*

				<ul>
					<li>McCormick School of Engineering,&nbsp;Department of Chemical and Biological Engineering</li>
				</ul>
				</li>
				<li>Aaron Morris</li>
				<li>William Corcoran</li>
			</ul>
			 <em>* Principal Investigator</em>
			
			<p ><strong>NU 2024-093</strong></p>

			<p ><strong>IP STATUS</strong></p>

			<p >US Patent Pending (<a href="https://patents.google.com/patent/US20260055177A1/en?oq=19%2f237%2c257" target="_blank">19/237,257</a>)</p>

			<p ><strong>DEVELOPMENT STAGE</strong></p>

			<p >TRL-3 Experimental Proof-of-Concept: In vitro demonstration validates the core function of synthetic IL-23 receptors.</p>
			
		
	


<p ><strong>BACKGROUND</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/2024-0931.png"  />Immune system dysfunction, particularly autoimmunity, affects millions worldwide. Interleukin 23 (IL-23) is an inflammatory cytokine secreted by activated immune cells that plays a key role in the development of inflammation, autoimmune disease, and the onset and progression of cancer. Several biologic drugs targeting IL-23 have been developed for treating autoimmune diseases including psoriasis and Crohn&rsquo;s disease. Although effective, these drugs are systemic in nature, only target one element of the inflammatory cascade, and require frequent injection, thus resulting in limited efficacy and imposing a high burden on patients. Cell therapies are a promising alternative for durable treatment of autoimmunity given they can be longer acting, can target and infiltrate specific tissues, and can be genetically engineered to deliver therapeutic products in response to specific environmental cues. However, for these therapies to fulfill that promise, the development of new receptors for cell engineering capable of sensing soluble cues and relaying that detection through orthogonal mechanisms independent of native pathways to trigger specific therapeutic functions is needed. </p>

<p ><strong >ABSTRACT</strong></p>

<p ><img alt="After 22 hours of treating cells with IL-10, ligand-treated conditions were significantly induced." src="https://nulive.technologypublisher.com/files/sites/picture151.jpg"  />Northwestern researchers have engineered synthetic receptors for interleukin-23 that convert natural soluble cytokine detection into a controlled, orthogonal signaling event. This technology converts human cytokine receptors into self-contained biosensors, preserving native ligand specificity while signaling through insulated, non-native pathways for safer, more programmable cell therapies. Its robust, modular architecture is tolerant to expression-level variability, supports multiplexed soluble-cue sensing and Boolean logic, and integrates cleanly with CARs and other effectors, thus reducing tuning burden and accelerating translation across cell types and delivery modalities. These receptors function in mammalian cells, demonstrate robust in vitro activity, and lay the groundwork for engineering tunable biosensors to program cellular responses in autoimmune and cancer immunotherapy applications.</p>

<p ><strong >APPLICATIONS</strong></p>

<ul >
	<li>Integration into CAR T cell therapies to enhance&nbsp;cell-based immunotherapies</li>
	<li>Programmable cell therapies to enable&nbsp;controlled therapeutic responses</li>
	<li>Biosensing to provides real-time monitoring of cytokine levels</li>
	<li>Research tool for cytokine signaling to facilitate&nbsp;studies on immune modulation</li>
</ul>

<p ><strong >ADVANTAGES</strong></p>

<ul >
	<li>Enhances specificity by offering&nbsp;orthogonal signaling that minimizes crosstalk with native pathways</li>
	<li>Durable response for&nbsp;long-lasting cell therapy effects compared to transient drug delivery</li>
	<li>Flexible design with adaptable architecture for diverse cytokine targets and applications</li>
	<li>Scalable manufacturing and integration ease&nbsp;into existing cell therapy production pipelines</li>
</ul>

<p ><strong >PUBLICATIONS</strong></p>

<ul >
	<li>Joshua Leonard et al., <a href="https://www.nature.com/articles/s41589-025-01986-1"  target="_blank">&quot;Conversion of natural cytokine receptors into orthogonal synthetic biosensors&quot;</a>, Nature, August 22, 2025</li>
	<li>Joshua Leonard et al., <a href="https://www.mccormick.northwestern.edu/news/articles/2025/08/building-smart-cell-sensors-for-safer-more-precise-cancer-therapies/"  target="_blank">&quot;Synthetic extracellular interleukin 23 biosensors&quot;</a>, Northwestern Engineering News, August 22, 2025</li>
</ul>

<p ><strong >CATEGORY/INDUSTRY PIPELINE</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2024-093.png"  />Biomarkers &amp; Biomedical Research Tools; Therapeutics</p>

<p ><strong >KEYWORDS</strong></p>

<p >synthetic receptor, IL-23, cytokine biosensor, cell therapy, autoimmunity, autoimmune disease, immunology, immunotherapy, orthogonal signaling, cell engineering, synthetic biology, targeted therapy, precision medicine</p>]]></description><pubDate>Tue, 14 Apr 2026 09:59:39 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Synthetic_Receptors_for_IL-23</guid><dataField:caseId>2024-093</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:18:20 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Autoimmune disease, Cell engineering, Cell therapy, Diagnostics, IBD - Inflammatory bowel disease, Immunology, Immunotherapy, Inflammation, Targeted therapy, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics| Life Sciences > Biomarkers & Biomedical Research Tools]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Responsive Probiotic Therapy for Local Detection and Treatment of IBD Flares</title><link>https://canberra-ip.technologypublisher.com/tech/Responsive_Probiotic_Therapy_for_Local_Detection_and_Treatment_of_IBD_Flares</link><description><![CDATA[<p ><strong>NU 2024-047</strong><br />
<br />
<strong>SHORT DESCRIPTION</strong></p>

<p >An engineered probiotic that senses intestinal inflammation via calprotectin and locally releases therapeutic antibodies in the gastrointestinal tract only during inflammatory flares.</p>


	
		
			<strong>INVENTORS</strong>

			<ul>
				<li>Arthur Prindle*

				<ul>
					<li>McCormick School of Engineering,&nbsp;Department of Chemical and Biological Engineering</li>
				</ul>
				</li>
				<li>Jonathan Xia</li>
			</ul>
			  <em>* Principal Investigator</em>
			
			<p ><strong>NU 2023-131, NU 2024-047</strong></p>

			<p ><strong>IP STATUS</strong></p>

			<p >Multiple US Patents pending (<a href="https://patents.google.com/patent/US20250034613A1/en?oq=18%2f775%2c012" target="_blank">18/775,012</a>;&nbsp;<a href="https://patents.google.com/patent/US20250339476A1/en?oq=19%2f198%2c291" target="_blank">19/198,291</a>)</p>

			<p ><strong>DEVELOPMENT STAGE</strong></p>

			<p >TRL-5 Prototype Validated in Relevant Environment: Calprotectin sensor performance has been confirmed using a DSS-induced colitis murine model.</p>
			
		
	


<p ><br />
<strong>BACKGROUND</strong></p>

<p ><img alt="Engineered E. coli Nissle 1917 (EcN) functions as an inflammation‑responsive sensor by detecting elevated calprotectin—an established clinical biomarker of IBD—and activating a GFP reporter only during intestinal flares. In healthy gut conditions, calprotectin levels remain low and the sensor strain stays inactive, whereas during an IBD flare, high calprotectin triggers GFP expression, enabling localized, real‑time reporting of disease activity." src="https://nulive.technologypublisher.com/files/sites/prindle_with_caption.png"  />Inflammatory bowel disease (IBD), including Crohn&rsquo;s disease and ulcerative colitis, is a chronic autoimmune condition marked by recurrent inflammation of the gastrointestinal (GI) tract, requiring long‑term management, which is associated with substantial morbidity, impaired quality of life, increased colorectal cancer risk, and significant healthcare costs. Globally, IBD affects an estimated 4.9 million people, with prevalence rising. While effective therapies exist, they are typically delivered systemically and can cause significant side effects due to prolonged immunosuppression. At the same time, disease monitoring relies on invasive or slow diagnostic methods, which can delay timely intervention during inflammatory flares. There is a critical need for therapeutic approaches that both detect intestinal inflammation noninvasively and deliver treatment locally, only when disease activity is present.&nbsp;</p>

<p ><br />
<strong>ABSTRACT</strong><br />
<img alt="Calprotectin-sensing EcN can reliably detect gut mucosal inflammation in vivo in the DSS-induced colitis mouse model. " src="https://nulive.technologypublisher.com/files/sites/prindle_2023-131.png"  />Northwestern researchers have developed an engineered probiotic capable of detecting markers indicative of active inflammation in the GI tract and releasing therapeutic antibodies in response for treatment of IBD. This invention integrates synthetic biology with microbial diagnostics. E. Coli Nissle 1917 (EcN)&mdash;a probiotic&nbsp;with established safety in humans&mdash;was engineered to produce and selectively release therapeutic antibodies in the GI tract only in the presence of calprotectin, the clinical gold standard biomarker of IBD. In both in vitro settings and a DSS-induced murine colitis model, the probiotic showed high sensitivity and specificity to inflammation. The platform distinguished active IBD from remission by quantifying reporter signals that track with clinical calprotectin levels. For disease management, the engineered probiotic can subsequently release a therapeutic antibody, such as anti-TNF-&alpha;.&nbsp;&nbsp;<br />
<br />
<strong>APPLICATIONS</strong></p>

<ul>
	<li>IBD Disease Activity Monitoring: Enables noninvasive tracking of gut inflammation.</li>
	<li>Early Intervention Strategies: Supports timely identification of IBD flares to prevent complications.</li>
	<li>IDB Disease Management: Enables&nbsp;precise, inflammation‑responsive medication delivery within the gastrointestinal tract.</li>
</ul>

<p ><br />
<strong>ADVANTAGES</strong></p>

<ul>
	<li>Noninvasive and rapid: Eliminates the need for colonoscopies while providing fast results.</li>
	<li>Highly sensitive and specific: Reduces&nbsp;systemic immunosuppression from IV infusions by enabling local, calprotectin-induced delivery of antibody therapeutics.</li>
	<li>Cost-effective: Reduces overall diagnostic expenses by streamlining monitoring processes.</li>
	<li>Real-time disease tracking: Supports immediate clinical decisions and proactive patient care.</li>
</ul>

<p ><br />
<strong>PUBLICATIONS</strong></p>

<ul>
	<li>Xia, J. Y.; Hepler, C.; Tran, P.; Waldeck, N. J.; Bass, J.; Prindle, A. <a href="https://doi.org/10.1073/pnas.2221121120" target="_blank">Engineered Calprotectin-Sensing Probiotics for IBD Surveillance in Humans</a> Proceedings of the National Academy of Sciences, 2023</li>
</ul>

<p ><br />
<strong>CATEGORY/INDUSTRY PIPELINE</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_prindle_2023-131_bundle.png"  />Healthcare Devices, Tools &amp; IT; Biomarkers &amp; Biomedical Research Tools; Therapeutics</p>

<p ><br />
<strong>KEYWORDS</strong></p>

<p >Inflammation, immunology, IBD, calprotectin, engineered probiotics, non-invasive monitoring, biosensor, synthetic biology, gut inflammation, diagnostics, autoimmunity, biologic, cell therapy, therapeutics</p>]]></description><pubDate>Tue, 14 Apr 2026 09:49:49 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Responsive_Probiotic_Therapy_for_Local_Detection_and_Treatment_of_IBD_Flares</guid><dataField:caseId>Prindle 2023-131</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 12:52:25 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Autoimmune disease, Biologic, Cell therapy, Diagnostics, Gastrointestinal and Hepatic disease, IBD - Inflammatory bowel disease, Immunology, Immunotherapy, Inflammation, Synthetic biology, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Active Electromagnetic Interference Suppression for Magnetic Resonance Imaging-Guided Interventions (Case No. 2026-217)</title><link>https://canberra-ip.technologypublisher.com/tech/Active_Electromagnetic_Interference_Suppression_for_Magnetic_Resonance_Imaging-Guided_Interventions_(Case_No._2026-217)</link><description><![CDATA[<p><strong>Summary:&nbsp;</strong><br />
<br />
UCLA researchers in the Department of Radiological Sciences have developed a software-based active electromagnetic interference suppression solution for real-time MRI-guided interventions.</p>

<p><strong>Background:&nbsp;</strong><br />
<br />
Microwave ablation (MWA) has emerged as the preferred thermal ablation modality for treating non-surgical patients with primary and metastatic liver malignancies. The clinical success of thermal ablation depends critically on image guidance to ensure sufficient ablation margins while minimizing collateral thermal damage. Traditional image guidance, using modalities such as computed tomography (CT) and ultrasound, is constrained by limited soft tissue contrast and relies on surrogate markers of the ablation zone progression that do not reliably capture true ablation margins. These limitations reduce procedural precision and hinder real-time assessment of thermal dose delivery. Magnetic resonance imaging (MRI)-guided MWA addresses these shortcomings by providing superior soft tissue visualization and enabling real-time, non-invasive temperature monitoring through MR thermometry. This combination enhances targeting accuracy, intra-procedural monitoring, and treatment control, positioning MRI-guided MWA as a highly promising modality for minimally invasive tumor management.&nbsp;</p>

<p>However, broader clinical adoption of MRI-guided MWA remains limited by electromagnetic interference (EMI) emitted from MWA systems during active operation. EMI contaminates MRI data, obscuring visualization of the microwave antenna, tissue structures, and ablation zone boundaries &mdash; increasing the risk of incomplete treatment or collateral thermal damage. Beyond MWA, EMI poses challenges whenever insufficiently shielded powered devices are introduced into the MRI scanner room, constraining the range of MRI-conditional tools and monitoring equipment that can be used during procedures. Existing EMI mitigation approaches rely on specialized hardware modifications (e.g., additional shielding layers or in-line filters) or require suspending energy delivery during image acquisition. These approaches increase system complexity, disrupt therapeutic protocols, and are impractical for routine clinical workflows. Therefore, there is a critical need for a streamlined solution that enables reliable EMI suppression and integrates seamlessly into clinical workflows for MRI-guided interventions.</p>

<p><strong>Innovation:&nbsp;</strong><br />
<br />
To overcome the limitations of existing EMI mitigation approaches, researchers at UCLA have developed a software-based active EMI suppression (AES) framework that restores MRI signal integrity without requiring specialized hardware modifications or workflow disruptions. The framework leverages an unloaded body array coil&mdash;an existing clinical MRI system component&mdash;to capture raw EMI signatures independently of primary imaging data. This architecture enables seamless integration into existing MRI infrastructure without interfering with image acquisition or procedural workflow. The system characterizes and models the EMI signal on a frame-by-frame basis and adaptively subtracts it from the primary imaging coil data, enabling dynamic, real-time EMI suppression during active microwave ablation.</p>

<p>In controlled testing environments, the technology achieved a 40-fold signal-to-noise ratio (SNR) improvement in phantoms and a 13-fold improvement in vivo, with an EMI suppression rate exceeding 92%. These gains restore image fidelity sufficiently to enable consistent intra-procedural MRI visualization of anatomical details and ablation zone boundaries. The AES framework also preserves thermometric accuracy, maintaining a mean absolute temperature error of &lt;1.4 &deg;C in heated regions and &lt;0.3 &deg;C in non-heated tissue. This level of accuracy supports thermal dose monitoring and helps protect surrounding healthy structures. By eliminating the need for specialized shielding hardware or procedural workarounds, this software-driven AES solution directly addresses key infrastructure and workflow barriers and could facilitate broader clinical adoption of MRI-guided MWA and other MRI-guided interventions affected by EMI.&nbsp;</p>

<p><strong>Potential Applications:</strong><br />
<br />
●&nbsp;&nbsp; &nbsp;MRI-guided Thermal and Non-Thermal Ablation<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;MWA, radiofrequency ablation, laser interstitial thermal therapy, focused ultrasound, cryoablation, pulsed field ablation, histotripsy<br />
●&nbsp;&nbsp; &nbsp;MRI-Guided Surgical &amp; Robotic Interventions<br />
●&nbsp;&nbsp; &nbsp;Interventional Oncology &amp; Cardiology&nbsp;<br />
●&nbsp;&nbsp; &nbsp;Neuromodulation &amp; Brain Interventions&nbsp;<br />
●&nbsp;&nbsp; &nbsp;High-Risk Anatomical Interventions (e.g., proximity to critical structures)&nbsp;<br />
●&nbsp;&nbsp; &nbsp;Relaxed MRI Suite Shielding Requirements&nbsp;<br />
●&nbsp;&nbsp; &nbsp;Expanded MRI-Conditional Device Integration (e.g., monitors, tools, implants)&nbsp;<br />
●&nbsp;&nbsp; &nbsp;Point-of-Care &amp; Low-Field MRI Environments</p>

<p><strong>Advantages:</strong><br />
<br />
●&nbsp;&nbsp; &nbsp;Streamlined Clinical Workflow<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;Continuous, real-time visualization<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;No pre-training or separate calibration needed<br />
●&nbsp;&nbsp; &nbsp;Seamless Hardware and Software Integration<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;Leverages standard, existing MRI receiver coils &mdash; no custom hardware<br />
&nbsp; &nbsp; &nbsp;○&nbsp;&nbsp; &nbsp;Software-only solution, readily integrable into vendor or open-source reconstruction pipelines<br />
●&nbsp;&nbsp; &nbsp;Superior Intra-procedural Image Quality Preservation<br />
●&nbsp;&nbsp; &nbsp;Enhanced Patient Safety During Interventional Procedures<br />
●&nbsp;&nbsp; &nbsp;Reliable Real-time MRI and MR Temperature Monitoring&nbsp;</p>

<p><strong>Development-To-Date:</strong><br />
<br />
First successful demonstration of the invention in controlled gel phantom and in vivo pig liver model</p>

<p><strong>Related Papers:</strong><br />
●&nbsp;&nbsp; &nbsp;Dai, Qing, et al. &ldquo;Active Electromagnetic Interference Suppression for Real-Time MR Thermometry During MR-Guided Microwave Ablation.&rdquo; Annual Meeting of the International Society for Magnetic Resonance in Medicine (ISMRM), 2025, Honolulu, Hawai&rsquo;i, USA, 0677.</p>

<p><strong>Reference: </strong><br />
<br />
UCLA Case No. 2026-217</p>

<p><strong>Lead Inventor: </strong><br />
<br />
Holden H. Wu<br />
&nbsp;</p>]]></description><pubDate>Tue, 14 Apr 2026 09:46:04 GMT</pubDate><author>marketing@tdg.ucla.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Active_Electromagnetic_Interference_Suppression_for_Magnetic_Resonance_Imaging-Guided_Interventions_(Case_No._2026-217)</guid><dataField:caseId>2026-217</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 09:46:04 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Holden</dataField:firstName><dataField:lastName>Wu</dataField:lastName><dataField:title>PROF-HCOMP</dataField:title><dataField:department>RADIOLOGICAL SCIENCES [1685]</dataField:department><dataField:emailAddress>holdenwu@mednet.ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Qing</dataField:firstName><dataField:lastName>Dai</dataField:lastName><dataField:title>Tech Fellow</dataField:title><dataField:department>RADIOLOGICAL SCIENCES [1685]</dataField:department><dataField:emailAddress>qdai@ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Nikolaus</dataField:firstName><dataField:lastName>Traitler</dataField:lastName><dataField:title>Business Development Officer (BDO)</dataField:title><dataField:department>TECHNOLOGY DEVELOPMENT GROUP [3094]</dataField:department><dataField:emailAddress>nick.traitler@tdg.ucla.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Software & Algorithms| Software & Algorithms > AI Algorithms| Software & Algorithms > Artificial Intelligence & Machine Learning| Software & Algorithms > Image Processing| Medical Devices| Medical Devices > Medical Imaging| Medical Devices > Medical Imaging > MRI| Life Science Research Tools| Life Science Research Tools > Microscopy And Imaging| Life Science Research Tools > Lab Equipment| Medical Devices > Monitoring And Recording Systems| Therapeutics| Therapeutics > CNS and Neurology| Therapeutics > Immunology And Immunotherapy| Therapeutics > Inflammation And Inflammatory Diseases| Mechanical| Mechanical > Instrumentation| Mechanical > Sensors| Electrical| Electrical > Electronics & Semiconductors| Electrical > Signal Processing| Electrical > Instrumentation| Electrical > Imaging]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Bi-specific Lipid Nanoparticles for Boosting Antitumor Immunity in Glioblastoma</title><link>https://canberra-ip.technologypublisher.com/tech/Bi-specific_Lipid_Nanoparticles_for_Boosting_Antitumor_Immunity_in_Glioblastoma</link><description><![CDATA[<p ><strong>NU 2022-151</strong></p>

<p ><strong>SHORT DESCRIPTION</strong></p>

<p >A bispecific lipid nanoparticle that bridges tumor-associated myeloid cells (TAMCs) and glioma cells by dual checkpoint blockade and simultaneously reprograms TAMCs into antitumor effectors via targeted delivery of a STING agonist.</p>


	
		
			<strong>INVENTORS</strong>

			<ul>
				<li>Maciej Lesniak*

				<ul>
					<li>Northwestern University Feinberg School of Medicine, Department of Neurological Surgery</li>
				</ul>
				</li>
				<li>Peng Zhang</li>
			</ul>
			 <em>* Principal Investigator</em>
			
			<p ><strong>NU 2022-151</strong></p>

			<p ><strong>IP STATUS</strong></p>

			<p >&nbsp;US Patent&nbsp;filed (19/122,639).</p>

			<p ><strong>DEVELOPMENT STAGE</strong></p>

			<p >TRL-5 Prototype Validated in Relevant Environment: Preclinical murine studies demonstrate significant antitumor efficacy when combined with radiotherapy.</p>
			
		
	


<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/blnp_sting_img.png"  /><strong>BACKGROUND</strong></p>

<p >Glioblastoma is the most common and highly aggressive primary malignant brain tumor, accounting for roughly half of all malignant brain tumors and about 12,000 new cases annually in the U.S. Standard-of-care remains maximal safe surgical resection followed by radiotherapy and temozolomide-based chemotherapy; however, with a 5‑year survival around 6&ndash;7% and median overall survival at about 12&ndash;18 months, glioblastoma remains the leading cause of brain tumor&ndash;related death and is responsible for the majority of deaths among primary brain tumor patients. Current glioblastoma treatments, including radiation therapy, often trigger immune resistance and promote tumor evasion through immune checkpoint upregulation, contributing to near-universal recurrence, and face challenges such as high treatment costs and limited efficacy, underscoring a critical need for new and more effective treatment strategies.</p>

<p ><strong>ABSTRACT</strong></p>

<p >Northwestern scientists developed a bispecific lipid nanoparticle (B-LNP) <strong><img alt="" src="https://nulive.technologypublisher.com/files/sites/2022-1512.png"  /></strong>that targets tumor-associated myeloid cells (TAMCs) and glioma cells via dual ligation of CD47 and PD-L1. The nanoparticle blocks these immune checkpoints and delivers a STING agonist (diABZI) to reprogram TAMCs into antitumor effectors. In preclinical murine models, the B-LNP, when combined with radiotherapy, increased phagocytosis and T cell activation leading to significant tumor regression.</p>

<p ><strong>APPLICATIONS</strong></p>

<ul >
	<li>Glioblastoma treatment: Enhances antitumor immune responses in brain tumors.</li>
	<li>Combination therapy with radiotherapy: Boosts radiation efficacy through immune reprogramming.</li>
	<li>Targeted immunotherapy: Delivers STING agonists directly to tumor-associated myeloid cells.</li>
	<li>Nanoparticle-mediated drug delivery: Improves precision and safety in immune checkpoint blockade.</li>
</ul>

<p ><strong>ADVANTAGES</strong></p>

<ul >
	<li>Enhances immune cell phagocytosis: Blocks dual immune checkpoints for focused antitumor activity.</li>
	<li>Synergizes with radiotherapy: Amplifies tumor regression when used with standard treatments.</li>
	<li>Promotes durable responses: Reprograms myeloid cells to sustain long-term antitumor immunity.</li>
	<li>Precision delivery: Targets specific immune cells, reducing off-target effects and improving safety.</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<ul >
	<li>&nbsp;&nbsp;Maciej Lesniak et al., <a href="https://www.nature.com/articles/s41467-023-37328-9" target="_blank">STING agonist-loaded, CD47/PD-L1-targeting nanoparticles potentiate antitumor immunity and radiotherapy for glioblastoma</a>.&nbsp;Nature Communications. Mar 23, 2023.</li>
</ul>

<p ><strong>CATEGORY/INDUSTRY PIPELINE</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2022-151.png"  />Healthcare Devices, Tools &amp; IT; Therapeutics</p>

<p ><strong >KEYWORDS</strong></p>

<p >Cancer, oncology, glioblastoma, brain cancer, bispecific lipid nanoparticles, immunotherapy, tumor-associated myeloid cells, STING agonist, immune checkpoint blockade, radiotherapy, nanoparticle, drug delivery, targeted therapy</p>]]></description><pubDate>Tue, 14 Apr 2026 09:35:47 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Bi-specific_Lipid_Nanoparticles_for_Boosting_Antitumor_Immunity_in_Glioblastoma</guid><dataField:caseId>2022-151</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 11:15:08 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Brain cancer, Cancer/Oncology, Drug delivery, Immunotherapy, Nanoparticle, Nanotechnology, Targeted therapy, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Recombinant Annexin Therapy for Muscle, Cardiac, and Neuronal Cell Membrane Repair</title><link>https://canberra-ip.technologypublisher.com/tech?title=Recombinant_Annexin_Therapy_for_Muscle%2c_Cardiac%2c_and_Neuronal_Cell_Membrane_Repair</link><description><![CDATA[<p class="subheader" ><strong>NU 2022-008</strong></p>

<p class="subheader" ><strong>SHORT DESCRIPTION</strong></p>

<p class="subheader" >An annexin-based biological therapeutic that enhances the body&#39;s natural cell membrane repair process to reduce skeletal muscle, cardiac, and neuronal cell death and preserve tissue function.</p>

<p class="subheader" ><strong>INVENTORS</strong></p>


	
		
			<strong>INVENTORS</strong>

			<ul>
				<li>Elizabeth McNally*
				<ul>
					<li>Feinberg School of Medicine, Department of Medicine (Cardiology Division)</li>
				</ul>
				</li>
				<li>Alexis Demonbreun
				<ul>
					<li>Feinberg School of Medicine, Department of Pharmacology</li>
				</ul>
				</li>
				<li>
				<ul>
				</ul>
				Robert Vassar

				<ul>
					<li>Feinberg School of Medicine, Department of Neurology</li>
				</ul>
				</li>
				<li>Dominic Fullenkamp</li>
				<li>Katherine Sadleir</li>
			</ul>
			<em>* Principal Investigator</em>
			
			<p ><strong>NU Tech ID:&nbsp;&nbsp;</strong>NU 2018-119, 2022-008</p>

			<p ><strong>IP STATUS</strong></p>

			<p >Multiple US Patents pending (<a href="https://patents.google.com/patent/US20220143136A1/en?oq=US-2022-0143136-A1" target="_blank">17/416,018</a>, <a href="https://patents.google.com/patent/US20250195609A1/en?oq=US-2025-0195609-A1" target="_blank">18/838,195</a>) and several OUS&nbsp;Patents granted (<a href="https://patents.google.com/patent/EP3897689B1/en?oq=3897689" target="_blank">3897689</a>) and pending (CA, AU, CN, JP).&nbsp;</p>

			<p ><strong>DEVELOPMENT STAGE</strong></p>

			<p >TRL-3 - Experimental Proof-of-Concept Active R&amp;D: Key functionalities have been validated in preclinical models.</p>
			
		
	


<p class="subheader" ><strong>BACKGROUND</strong></p>

<p ><strong><img alt="" src="https://nulive.technologypublisher.com/files/sites/image_for_ncs2.png"  /></strong>Cell membrane integrity is critical for cell survival and function, and its disruption in excitable tissues such as muscle, cardiac, and neuronal cells, disturbs ionic homeostasis, signaling, and cell survival. &nbsp;When repair mechanisms are impaired or defective, membrane disruption drives tissue loss and organ dysfunction and contributes to the development of various chronic conditions including Duchenne and Becker muscular dystrophies, ischemic injury, and membrane‑fragility cardiomyopathies, and neuropathies resulting from traumatic brain injury, spinal cord injury, and post‑cardiac arrest brain injury. Together, these conditions affect millions of people each year. Existing therapies focus on slowing disease progression and improving downstream consequences, but leave the initial membrane injury and defective repair largely unaddressed, and currently there are no broadly approved therapies aimed at enhancing of plasma membrane repair. The high cost and limited efficacy of current treatments demonstrate the need for improved membrane repair solutions</p>

<p class="subheader" ><strong>ABSTRACT</strong></p>

<p >This technology developed by Northwestern researchers provides compositions and methods for treatment of cellular membrane injury. Annexins are essential for the calcium-dependent process of sealing membrane breaches. This invention entails administering a recombinant version of the annexin A6 protein to directly bolster the endogenous membrane repair machinery in cardiac, neuronal, and muscle tissues. Preclinical studies in animal models reveal that annexin A6 rapidly localizes at injury sites to form repair caps. The technology leverages both intracellular and extracellular mechanisms to enhance membrane resealing. These results support its potential to restore cellular integrity and function following injury.</p>

<p class="subheader" ><strong>APPLICATIONS</strong></p>

<ul>
	<li>Cardiac repair: Treatment following acute myocardial injury.</li>
	<li>Neurological repair: Management of traumatic brain and spinal cord injuries.</li>
	<li>Muscular dystrophy management: Enhancing membrane repair in chronic muscle disorders.</li>
	<li>Preventive therapy: Reducing cell damage in high-risk patients.</li>
</ul>

<p class="subheader" ><strong>ADVANTAGES</strong></p>

<ul>
	<li>Accelerates membrane repair: Rapidly localizes to injury sites to reduce repair time.</li>
	<li>Reduces long-term tissue damage: Minimizes secondary cell loss post injury.</li>
	<li>Enhances recovery: Supports cell survival and functional recovery.</li>
	<li>Broad applicability: Serves both acute and chronic conditions across multiple tissues.</li>
</ul>

<p ><strong>PUBLICATIONS</strong></p>

<ul>
	<li>Demonbreun AR, Bogdanovic E, Vaught LA, Reiser NL, Fallon KS, Long AM, Oosterbaan CC, Hadhazy M, Page PG, Joseph PRB, Cowen G, Telenson AM, Khatri A, Sadleir KR, Vassar R, McNally EM, <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC9431694/" target="_blank">A conserved annexin A6-mediated membrane repair mechanism in muscle, heart and nerve</a>, JCI Insight, 2022 Jul 22.</li>
</ul>

<p class="subheader" ><strong>CATEGORY/INDUSTRY PIPELINE</strong></p>

<p ><img alt="" src="https://nulive.technologypublisher.com/files/sites/qr-code_2018-119_bundle.png"  />Therapeutics; Biomarkers &amp; Biomedical Research Tools</p>

<p class="subheader" ><strong>KEYWORDS</strong></p>

<p >Annexin, membrane repair, cardiac injury, neuronal injury, recombinant protein, therapeutic agent, acute therapy, chronic disorder, cell membrane, cardiovascular, muscular dystrophy, TBI, SCI, DMD, MI, reperfusion injury, rare disease</p>]]></description><pubDate>Tue, 14 Apr 2026 09:32:34 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech?title=Recombinant_Annexin_Therapy_for_Muscle%2c_Cardiac%2c_and_Neuronal_Cell_Membrane_Repair</guid><dataField:caseId>McNally 2022-008</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 12:52:51 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Biologic, Cardiomyopathy, DMD - Duchenne muscular dystrophy, Inflammation, Membrane injury and repair, Neurodegenerative disease, Rare diseases, SCI - Spinal cord injury, TBI - Traumatic brain injury, Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Michael</dataField:firstName><dataField:lastName>Fiske</dataField:lastName><dataField:title>Invention Manager</dataField:title><dataField:department>MED-NUIN</dataField:department><dataField:emailAddress>michael.fiske@northwestern.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life Sciences > Therapeutics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>A Smartwatch-integrable, non-invasive RF bioimpedance wearable system for continuous, equitable blood pressure monitoring</title><link>https://canberra-ip.technologypublisher.com/tech?title=A_Smartwatch-integrable%2c_non-invasive_RF_bioimpedance_wearable_system_for_continuous%2c_equitable_blood_pressure_monitoring</link><description><![CDATA[<p>This technology is a smartwatch-compatible, low-power wearable that uses radio frequency bioimpedance and AI to continuously and non-invasively monitor blood pressure, offering accurate, skin color-independent readings and robust performance compared to traditional optical sensors.</p>

<h2>Background</h2>

<p>Blood pressure (BP) monitoring is a cornerstone of cardiovascular health management, as hypertension is a leading risk factor for heart disease, stroke, and other serious conditions. Traditionally, BP is measured intermittently using inflatable cuffs, which can be uncomfortable and impractical for continuous monitoring. The growing prevalence of wearable health devices, such as smartwatches, has driven demand for non-invasive, continuous BP monitoring solutions that are comfortable, unobtrusive, and suitable for everyday use. Continuous BP monitoring can provide valuable insights into an individual&rsquo;s cardiovascular health, enable early detection of hypertension, and support personalized healthcare interventions. As such, there is a significant need for wearable technologies that can deliver accurate, reliable, and equitable BP measurements across diverse populations.</p>

<p>Current approaches to wearable BP monitoring predominantly rely on photoplethysmography (PPG), an optical technique that estimates BP by analyzing blood volume changes in the microvascular bed of tissue. However, PPG-based systems face several critical limitations. Their accuracy is often compromised in individuals with darker skin tones due to reduced optical penetration and weaker light-artery interactions, leading to biased readings and inequitable healthcare outcomes. Additionally, PPG sensors are highly susceptible to motion artifacts, which can distort measurements during daily activities and reduce reliability. Integration of PPG sensors into wearable devices also requires precise alignment and intimate skin contact, which can be uncomfortable and limit user compliance. These challenges highlight the need for alternative, robust, and equitable BP monitoring methods that can overcome the shortcomings of current optical and contact-based technologies.</p>

<h2>Technology Description</h2>

<p>This technology is a smartwatch-integrable, low-power wearable system designed for continuous, non-invasive blood pressure monitoring using radio frequency (RF) bioimpedance and artificial intelligence. By repurposing a standard inverted F-type Wi-Fi antenna from a commercial smartwatch and mounting it on a 3D-printed nylon substrate within a watch strap, the system operates in a non-contact manner to measure the reflection parameter (S11) of an RF signal at the tissue-artery interface. This allows it to detect changes in arterial bioimpedance, which correlate with blood flow and blood pressure. The system extracts both frequency and time-domain features from these bioimpedance signals and processes them with an AdaBoosted Decision Tree regressor to estimate systolic and diastolic blood pressure. The approach is robust to variations in skin color, less susceptible to motion artifacts than optical methods, and is easily integrated into existing smartwatch infrastructure, achieving accuracy comparable to medical-grade photoplethysmography (PPG) sensors and meeting BHS/AAMI standards.</p>

<p>What differentiates this technology is its unique combination of RF bioimpedance sensing and AI-driven analysis, which overcomes significant limitations of current wearable blood pressure monitors, particularly those relying on PPG. Unlike PPG, which can be biased by skin pigmentation and is sensitive to motion, this RF-based solution provides equitable, reliable measurements across diverse populations and in real-world conditions. Its non-contact design enhances user comfort and device durability, while leveraging existing smartwatch hardware simplifies manufacturing and integration, reducing cost and complexity. Preliminary studies demonstrate that its accuracy rivals medical-grade devices, with mean absolute errors well within clinical standards. The platform&rsquo;s adaptability to other wearable forms, such as rings, and its potential for broader health monitoring applications&mdash;ranging from stress and mood detection to pharmaceutical studies&mdash;further distinguish it as a transformative advancement in wearable health technology.</p>

<h2>Benefits</h2>

<ul>
	<li>Continuous, non-invasive blood pressure monitoring integrated into a smartwatch form factor</li>
	<li>Robust to skin color variations, eliminating bias common in optical PPG-based devices</li>
	<li>Non-contact measurement enhances user comfort and reduces need for precise sensor placement</li>
	<li>Lower power consumption suitable for wearable, continuous monitoring</li>
	<li>Reduced susceptibility to motion artifacts compared to optical and radar methods</li>
	<li>Utilizes existing smartwatch Wi-Fi antennas for simplified integration and reduced system complexity</li>
	<li>Achieves clinically relevant accuracy meeting BHS and AAMI standards</li>
	<li>Potential for expansion to other health monitoring applications such as stress, hydration, and pharmaceutical effects</li>
</ul>

<h2>Commercial Applications</h2>

<ul>
	<li>Continuous blood pressure monitoring</li>
	<li>Remote hypertension management</li>
	<li>Equitable health tracking wearables</li>
	<li>Population health analytics</li>
	<li>Pharmaceutical effect monitoring</li>
</ul>

<h2>Additional Information</h2>

<p>This wearable system continuously monitors blood pressure non-invasively. It repurposes a smartwatch Wi-Fi antenna to measure radio frequency bioimpedance (S11) at the tissue-artery interface. Extracted frequency and time-domain features from these signals are processed by an AdaBoosted Decision Tree regressor to estimate systolic and diastolic BP. This RF-based approach offers robustness to skin color and motion artifacts.</p>

<h2>Intellectual Property</h2>

<p><a href="https://patents.google.com/patent/WO2026025035A1/en?oq=PCT%2fUS2025%2f039271+" target="_blank">PCT/US2025/039271 </a></p>

<p>&nbsp;</p>

<p>&nbsp;</p>]]></description><pubDate>Tue, 14 Apr 2026 08:21:19 GMT</pubDate><author>intranet@discoveries.utexas.edu</author><guid>https://canberra-ip.technologypublisher.com/tech?title=A_Smartwatch-integrable%2c_non-invasive_RF_bioimpedance_wearable_system_for_continuous%2c_equitable_blood_pressure_monitoring</guid><dataField:caseId>8475 AKI</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 08:21:19 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Deji</dataField:firstName><dataField:lastName>Akinwande</dataField:lastName><dataField:title>Associate Professor</dataField:title><dataField:department>Electrical and Computer Engineering</dataField:department><dataField:emailAddress>deji@ece.utexas.edu</dataField:emailAddress><dataField:phoneNumber>512-471-4345</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Neelotpala</dataField:firstName><dataField:lastName>Kumar</dataField:lastName><dataField:title>Graduate student</dataField:title><dataField:department>ECE</dataField:department><dataField:emailAddress>neelotk@utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Solomon</dataField:firstName><dataField:lastName>Leo</dataField:lastName><dataField:title>Research Assistant</dataField:title><dataField:department>Chemical Engineering</dataField:department><dataField:emailAddress>Solomon.leo@utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Jiahui</dataField:firstName><dataField:lastName>Zhao</dataField:lastName><dataField:title>Doctoral Student</dataField:title><dataField:department>Kinesiology and Health Education</dataField:department><dataField:emailAddress>jiahzhao@utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Sophie</dataField:firstName><dataField:lastName>Lalande</dataField:lastName><dataField:title>Assistant Professor</dataField:title><dataField:department>Kinesiology and Health Education</dataField:department><dataField:emailAddress>sophie.lalande@austin.utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jacob</dataField:firstName><dataField:lastName>Grohman</dataField:lastName><dataField:title>Business Development Specialist</dataField:title><dataField:department>Life Sciences</dataField:department><dataField:emailAddress>jacob.grohman@discoveries.utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Life sciences > Medical technology > Medical devices]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>True</dataField:isFeatured></item><item><title>Vox Deorum</title><link>https://canberra-ip.technologypublisher.com/tech/Vox_Deorum</link><description><![CDATA[<p>This technology is a hybrid large language model (LLM) that connects artificial intelligence (AI) agents into open source 4X and grand strategy games. Vox Deorum enables the observation and comparison of reasoning and decision-making across different AI agents within a game environment, while also facilitating interaction between human players and AI agents. The technology has the potential to enhance human&ndash;AI decision making, support the evaluation, training, and optimization of generative AI and agent-based systems, and drive innovation in the design of strategy games.&nbsp;<br />
<br />
<strong>Background:&nbsp;</strong><br />
Large Language Models&rsquo; capacity to reason in natural language makes them promising for use in 4X (eXploration, eXpansion, eXploitation, and eXtermination) and grand strategy games. LLMs could enable more natural human-AI gameplay interactions such as collaboration and negotiation. However, these games can be challenging due to their complexity and long-horizon nature, which can affect LLMs&rsquo; latency and create enormous costs. Vox Deorum addresses this through a hybrid structure that uses LLMs for strategic decision making while specialized subsystems handle tactical execution.<br />
<br />
<strong>Applications:&nbsp;</strong></p>

<ul>
	<li>Strategy games / grand strategy games / 4X games</li>
	<li>AI in games</li>
	<li>AI agents</li>
	<li>Open-source games</li>
	<li>Video game development</li>
</ul>

<p><br />
<strong>Advantages:&nbsp;</strong></p>

<ul>
	<li>Improved decision making in games</li>
	<li>Evolving game design with AI</li>
	<li>Enhanced user experience in games</li>
	<li>Opportunities for human&ndash;AI interaction during gameplay</li>
</ul>]]></description><pubDate>Mon, 13 Apr 2026 09:28:42 GMT</pubDate><author>JianlingL@tla.arizona.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Vox_Deorum</guid><dataField:caseId>UA26-182</dataField:caseId><dataField:lastUpdateDate>Mon, 13 Apr 2026 09:28:42 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>John</dataField:firstName><dataField:lastName>Chen</dataField:lastName><dataField:title></dataField:title><dataField:department>College of Information Science</dataField:department><dataField:emailAddress>johnchen@arizona.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lyndsay</dataField:firstName><dataField:lastName>Troyer</dataField:lastName><dataField:title><![CDATA[Licensing Associate, Software & Copyright]]></dataField:title><dataField:department></dataField:department><dataField:emailAddress>LyndsayT@arizona.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Creative Works & Copyright| Technology Classifications > Software & Information Technology > Open Source]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Benchmarking Off-Grid Edge AI on Legacy Devices for Sustainable Deployment</title><link>https://canberra-ip.technologypublisher.com/tech/Benchmarking_Off-Grid_Edge_AI_on_Legacy_Devices_for_Sustainable_Deployment</link><description><![CDATA[<p>This technology presents a sustainable, off-grid edge AI system that leverages legacy devices and renewable energy to enable intelligent computing in resource-limited environments.&nbsp;</p>

<p>Background: <br />
Traditional artificial intelligence infrastructures depend heavily on continuous internet connectivity and advanced, energy-demanding hardware, restricting their deployment in rural or underdeveloped regions. Additionally, many areas lack the necessary infrastructure to support such systems, leading to limited access to AI-driven solutions. There is a growing need to create efficient, low-cost, and eco-friendly AI platforms that can operate autonomously in off-grid settings without compromising performance or privacy. This technology was developed to address these challenges by rethinking AI deployment in ways that are sustainable, inclusive, and adaptable to existing hardware resources.</p>

<p>Technology Overview: &nbsp;<br />
This innovation introduces a modular edge AI architecture capable of running entirely off-grid through integration with renewable energy sources like solar and wind power. It benchmarks distributed AI inference across a range of hardware platforms, including single-board computers and GPU-accelerated devices, to optimize the balance between budget constraints, available computational resources, energy consumption, and processing performance. A distinguishing feature is its platform-agnostic design, enabling the use of legacy smartphones repurposed as sensor interfaces. This not only reduces electronic waste but also enhances user privacy by minimizing data transmission over networks. The system supports multiple deployment modes to adapt to varied operational scenarios and resource availability. Its versatility has been proven through field trials in diverse environments like the Adirondacks, highlighting its potential for real-world applications. By enabling intelligent data processing at the edge without reliance on constant connectivity, this technology facilitates equitable access to AI capabilities while promoting environmental sustainability.&nbsp;</p>

<p>https://suny.technologypublisher.com/files/sites/adobestock_857930286.jpeg<br />
Photo for reference only, not a depiction of the invention.</p>

<p>Advantages: &nbsp;<br />
&bull;&nbsp;&nbsp; &nbsp;Energy Efficiency: Operates entirely on modular renewable energy sources, reducing dependence on fossil fuels and grid power.<br />
&bull;&nbsp;&nbsp; &nbsp;Platform Agnostic: Compatible with a wide range of hardware, including repurposed legacy devices, ensuring broad accessibility and cost-effectiveness.<br />
&bull;&nbsp;&nbsp; &nbsp;Reduced E-Waste: Extends the usable life of existing devices, minimizing environmental impact and resource consumption.<br />
&bull;&nbsp;&nbsp; &nbsp;Enhanced Privacy: Localized data processing limits exposure of sensitive information by reducing the need for cloud connectivity.<br />
&bull;&nbsp;&nbsp; &nbsp;Flexible Deployment: Supports multiple modes to adapt to different hardware capacities and deployment environments.<br />
&bull;&nbsp;&nbsp; &nbsp;Validated in Real-World Conditions: Proven effectiveness through field trials in remote and resource-constrained locations.&nbsp;</p>

<p>Applications: &nbsp;<br />
&bull;&nbsp;&nbsp; &nbsp;Education: Enabling AI-driven educational tools and resources in remote areas lacking stable internet access.<br />
&bull;&nbsp;&nbsp; &nbsp;Agriculture: Supporting smart farming practices through localized data analysis and sensor integration.<br />
&bull;&nbsp;&nbsp; &nbsp;Emergency Response: Facilitating autonomous and reliable AI systems for disaster and wilderness survival scenarios.<br />
&bull;&nbsp;&nbsp; &nbsp;Environmental Monitoring: Deploying edge AI to collect and analyze ecological data in off-grid natural reserves.<br />
&bull;&nbsp;&nbsp; &nbsp;Rural Development: Providing infrastructure-independent intelligent solutions to improve quality of life and economic opportunities.&nbsp;</p>

<p>Intellectual Property Summary: <br />
Proprietary know-how; patent strategy pending</p>

<p>Stage of Development: <br />
TRL 4</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>]]></description><pubDate>Mon, 13 Apr 2026 09:28:03 GMT</pubDate><author>IEA@rfsuny.org</author><guid>https://canberra-ip.technologypublisher.com/tech/Benchmarking_Off-Grid_Edge_AI_on_Legacy_Devices_for_Sustainable_Deployment</guid><dataField:caseId>270-2427</dataField:caseId><dataField:lastUpdateDate>Tue, 14 Apr 2026 07:29:52 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>This technology presents a sustainable, off-grid edge AI system that leverages legacy devices and renewable energy to enable intelligent computing in resource-limited environments.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background>Traditional artificial intelligence infrastructures depend heavily on continuous internet connectivity and advanced, energy-demanding hardware, restricting their deployment in rural or underdeveloped regions. Additionally, many areas lack the necessary infrastructure to support such systems, leading to limited access to AI-driven solutions. There is a growing need to create efficient, low-cost, and eco-friendly AI platforms that can operate autonomously in off-grid settings without compromising performance or privacy. This technology was developed to address these challenges by rethinking AI deployment in ways that are sustainable, inclusive, and adaptable to existing hardware resources.</dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology>This innovation introduces a modular edge AI architecture capable of running entirely off-grid through integration with renewable energy sources like solar and wind power. It benchmarks distributed AI inference across a range of hardware platforms, including single-board computers and GPU-accelerated devices, to optimize the balance between budget constraints, available computational resources, energy consumption, and processing performance. A distinguishing feature is its platform-agnostic design, enabling the use of legacy smartphones repurposed as sensor interfaces. This not only reduces electronic waste but also enhances user privacy by minimizing data transmission over networks. The system supports multiple deployment modes to adapt to varied operational scenarios and resource availability. Its versatility has been proven through field trials in diverse environments like the Adirondacks, highlighting its potential for real-world applications. By enabling intelligent data processing at the edge without reliance on constant connectivity, this technology facilitates equitable access to AI capabilities while promoting environmental sustainability.</dataField:Technology><dataField:Picture>https://suny.technologypublisher.com/files/sites/adobestock_857930286.jpeg</dataField:Picture><dataField:PictureRef>Photo for reference only, not a depiction of the invention.</dataField:PictureRef><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[&bull;&nbsp;&nbsp; &nbsp;Energy Efficiency: Operates entirely on modular renewable energy sources, reducing dependence on fossil fuels and grid power.<br />
&bull;&nbsp;&nbsp; &nbsp;Platform Agnostic: Compatible with a wide range of hardware, including repurposed legacy devices, ensuring broad accessibility and cost-effectiveness.<br />
&bull;&nbsp;&nbsp; &nbsp;Reduced E-Waste: Extends the usable life of existing devices, minimizing environmental impact and resource consumption.<br />
&bull;&nbsp;&nbsp; &nbsp;Enhanced Privacy: Localized data processing limits exposure of sensitive information by reducing the need for cloud connectivity.<br />
&bull;&nbsp;&nbsp; &nbsp;Flexible Deployment: Supports multiple modes to adapt to different hardware capacities and deployment environments.<br />
&bull;&nbsp;&nbsp; &nbsp;Validated in Real-World Conditions: Proven effectiveness through field trials in remote and resource-constrained locations.]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[&bull;&nbsp;&nbsp; &nbsp;Education: Enabling AI-driven educational tools and resources in remote areas lacking stable internet access.<br />
&bull;&nbsp;&nbsp; &nbsp;Agriculture: Supporting smart farming practices through localized data analysis and sensor integration.<br />
&bull;&nbsp;&nbsp; &nbsp;Emergency Response: Facilitating autonomous and reliable AI systems for disaster and wilderness survival scenarios.<br />
&bull;&nbsp;&nbsp; &nbsp;Environmental Monitoring: Deploying edge AI to collect and analyze ecological data in off-grid natural reserves.<br />
&bull;&nbsp;&nbsp; &nbsp;Rural Development: Providing infrastructure-independent intelligent solutions to improve quality of life and economic opportunities.]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus>Proprietary know-how; patent strategy pending</dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>TRL 4</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:inventorList><dataField:inventor><dataField:firstName>Asela</dataField:firstName><dataField:lastName>Abeya</dataField:lastName><dataField:title>Lecturer</dataField:title><dataField:department></dataField:department><dataField:emailAddress>abeyaa@sunypoly.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Nick</dataField:firstName><dataField:lastName>LeJeune</dataField:lastName><dataField:title>Assistant Professor</dataField:title><dataField:department><![CDATA[Interactive Media & Game Design]]></dataField:department><dataField:emailAddress>lejeunc@sunypoly.edu</dataField:emailAddress><dataField:phoneNumber>(315) 351-3576</dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>artificial intelligence for social good, benchmark, Energy-Aware Inference, Large language models, Legacy-Phone Clients, Modular Edge AI, Off-Grid AI, renewable energy, solar energy, Sustainable Computing, Technologies, wind energy, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Austin</dataField:firstName><dataField:lastName>Winter</dataField:lastName><dataField:title>Senior Associate, IP and Licensing, Patent Agent</dataField:title><dataField:department><![CDATA[Industry & External Affairs]]></dataField:department><dataField:emailAddress>austin.winter@rfsuny.org</dataField:emailAddress><dataField:phoneNumber>(518) 434-7022</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > SUNY Polytechnic Institute| Technology Classifications > Artificial Intelligence| Technology Classifications > Energy Conservation]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Hardware-Based Security Gateway for IoT and Wireless Sensor Networks</title><link>https://canberra-ip.technologypublisher.com/tech/Hardware-Based_Security_Gateway_for_IoT_and_Wireless_Sensor_Networks</link><description><![CDATA[<h3><em>Protects Iot Data by Shifting Security Processing from Software to a Secure Model for Faster, Lower-Latency Communication</em></h3>

<p>This hardware-based security gateway for Internet of Things (IoT) and wireless sensor networks protects data by shifting security processing from software to a secure module, enabling faster, lower-latency communication and thermal performance while strengthening security. Globally, more than 29 billion devices are connected to the internet, many of them operating as resource-constrained sensors and edge nodes. These heterogeneous devices often rely on software-only security, which increases processor load, power use, and delay and exposes keys to malware and physical tampering. As deployments expand to dynamic, infrastructure-intensive environments such as industrial and remote sites, gateways must secure increasingly large data streams between device networks, edge systems, and cloud services. However, traditional software-only gateways fail to secure communication without degrading performance.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida developed a hardware-based security gateway for IoT and wireless sensor networks that integrates a dedicated hardware security module (HSM) to isolate cryptographic operations from the main processor. By implementing hardware-based encryption, key storage, and tamper detection, the system improves performance while enhancing security across heterogeneous IoT deployments. This security gateway has been validated in infrastructure-intensive environments such as construction sites and supports broader industrial and edge computing applications.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>Secure, low-latency edge gateway that protects IoT sensor data and control traffic for construction sites and other industrial edge computing environments</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Off-loads security processing to dedicated hardware, reducing network latency and network connection time by nearly 6% compared to software-based security</li>
	<li>Lowers encryption time by 44% and decryption delay by 57%, enabling faster data transfer to edge and cloud analytics platforms</li>
	<li>Shifts cryptographic processing to hardware, lowering gateway operating temperature and improving long-term system reliability</li>
	<li>Protects cryptographic keys in isolated hardware, preventing extraction even if software is compromised</li>
	<li>Detects physical tampering at the gateway level, enabling automatic alerts that support real-time responses to hardware attacks and intrusion attempts</li>
	<li>Secures IoT communications in remote and infrastructure-heavy environments, supporting deployment in construction and other industrial settings</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>This hardware-based security system for IoT and wireless sensor networks secures data by integrating a hardware security module (HSM) into an IoT gateway that connects diverse devices to edge and cloud networks. The gateway software manages device communication, while the HSM performs all cryptographic operations, including key generation, secure storage, encryption, decryption, and digital signing, independent of the main processor. The gateway routes incoming device data through the HSM, which enforces encryption and authentication before transmission beyond the local network. The security module generates and stores cryptographic keys entirely within hardware, preventing exposure to system memory or application software. The HSM also monitors physical integrity, enabling detection of tampering or unauthorized access.</p>]]></description><pubDate>Mon, 13 Apr 2026 07:20:10 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Hardware-Based_Security_Gateway_for_IoT_and_Wireless_Sensor_Networks</guid><dataField:caseId>MP26029</dataField:caseId><dataField:lastUpdateDate>Mon, 13 Apr 2026 07:28:45 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Aaron</dataField:firstName><dataField:lastName>Costin</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>DCP-CONSTRUCTION MGMT</dataField:department><dataField:emailAddress>aaron.costin@ufl.edu</dataField:emailAddress><dataField:phoneNumber>352-273-1150</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Janise</dataField:firstName><dataField:lastName>McNair</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>EG-ELECTRICAL / COMPUTER ENG</dataField:department><dataField:emailAddress>jymcnair@ufl.edu</dataField:emailAddress><dataField:phoneNumber>352-392-0911</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Kyle</dataField:firstName><dataField:lastName>Morman</dataField:lastName><dataField:title>PhD Candidate</dataField:title><dataField:department>DCP-RINKER SCH OF CONSTR MGMT</dataField:department><dataField:emailAddress>kyle.morman420@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Quadri</dataField:firstName><dataField:lastName>Abiru</dataField:lastName><dataField:title>Former Student</dataField:title><dataField:department>UF ENGINEERING - ELECTRICAL / COMPUTER ENG</dataField:department><dataField:emailAddress>quadriabiru@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Uday Kiran</dataField:firstName><dataField:lastName>Sunkara</dataField:lastName><dataField:title>Former Employee</dataField:title><dataField:department>ELECTRICAL AND COMPUTER ENGINEERING</dataField:department><dataField:emailAddress>udaysunkara02@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Electrical| Technology Classifications > Software > Others]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>AI-Powered Skill Assessment and Credentialing System for Interactive Digital Applications</title><link>https://canberra-ip.technologypublisher.com/tech/AI-Powered_Skill_Assessment_and_Credentialing_System_for_Interactive_Digital_Applications</link><description><![CDATA[<div ><strong>Invention Description</strong></div>

<div >Interactive digital applications like video games, simulations, and virtual training environments are valuable tools for learning and professional development, offering dynamic environments that facilitate complex problem-solving and collaboration in dynamic, unstructured situations. However, effectively measuring the knowledge acquired within these experiences is difficult, as current evaluation systems are inadequate. Adapting these applications for assessment is often impossible or impractical, especially when dealing with proprietary software lacking available source code. As a result, assessment is typically limited to specialized educational tools that use pre-existing logging mechanisms, rather than broader, immersive environments</div>

<div >&nbsp;</div>

<div >Researchers at Arizona State University have created a novel AI-based assessment and credentialling system that captures and analyzes user interaction data, including video and audio, from games or simulations without requiring source code access. It employs computer vision and natural language processing to interpret user inputs and application events, mapping demonstrated competencies to skill tags within a personalized knowledge graph. Credentials are issued when skills are verified, enabling integration with external platforms while ensuring privacy through anonymization and encryption. The system supports both real-time and post-activity assessments across diverse domains.</div>

<div >&nbsp;</div>

<div >This technology offers an innovative AI-based system to evaluate learning by analyzing user interactions with unmodified digital applications to generate skill credentials.</div>

<div >&nbsp;</div>

<div ><strong>Potential Applications</strong></div>

<ul>
	<li >Educational platforms for formative and summative assessment</li>
	<li >Military and professional training simulations</li>
	<li >Esports player skill evaluation and development</li>
	<li >Corporate training and certification programs</li>
	<li >Gamified learning environments and serious games</li>
</ul>

<div ><strong>Benefits and Advantages</strong></div>

<ul>
	<li >Non-invasive integration with existing applications without source code access</li>
	<li >Multimodal data capture including video, audio, and interaction logs</li>
	<li >Advanced AI techniques for accurate skill recognition and semantic mapping</li>
	<li >Personalized skill tracking through user-specific knowledge graphs</li>
	<li >Real-time and post hoc analysis capabilities</li>
	<li >Privacy-preserving mechanisms including data anonymization and encryption</li>
	<li >Seamless credential issuance and external system integration</li>
</ul>]]></description><pubDate>Fri, 10 Apr 2026 17:51:56 GMT</pubDate><author>ip@skysonginnovations.com</author><guid>https://canberra-ip.technologypublisher.com/tech/AI-Powered_Skill_Assessment_and_Credentialing_System_for_Interactive_Digital_Applications</guid><dataField:caseId>M25-283P</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 17:51:56 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Mark</dataField:firstName><dataField:lastName>Ollila</dataField:lastName><dataField:title>Program Director and Professor of Practice</dataField:title><dataField:department>Herberger Institute for Design and the Arts</dataField:department><dataField:emailAddress>mark.ollila@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Mark</dataField:firstName><dataField:lastName>Naufel</dataField:lastName><dataField:title>Director of Strategic Projects</dataField:title><dataField:department>Knowledge Enterprise</dataField:department><dataField:emailAddress>Mark@primer.net</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Elina</dataField:firstName><dataField:lastName>Ollila</dataField:lastName><dataField:title>Professor of Practice</dataField:title><dataField:department>School of Arts, Media and Engineering</dataField:department><dataField:emailAddress>elina.ollila@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Physical Sciences</dataField:firstName><dataField:lastName>Team</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName>Artificial Intelligence/Machine Learning| Educational| Physical Science</dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Smart Low Power ECG Patch with Integrated Real Time Cardiac Analytics</title><link>https://canberra-ip.technologypublisher.com/tech/Smart_Low_Power_ECG_Patch_with_Integrated_Real_Time_Cardiac_Analytics</link><description><![CDATA[<p>This wearable ECG patch offers continuous heart monitoring while fixing common issues with current devices, such as bulky designs, short battery life, and missed data when signals are sent elsewhere for processing. By analyzing data directly on the device, it reduces power use and provides real-time heart rate, HRV, and irregular heartbeat information in a small, comfortable patch designed for long-term wear.</p>

<p>&nbsp;</p>

<p>Background: <br />
Ambulatory ECG monitoring systems often require bulky hardware, frequent battery changes, or off board signal processing that causes data gaps, missed alerts, and degraded signal fidelity. Noise, motion artifacts, and static transmission schemes further reduce reliability, while few devices integrate real time analytics with adaptive power management in a discreet, wearable patch.</p>

<p>&nbsp;</p>

<p>Technology Overview: <br />
This invention is a flexible two lead ECG patch powered by a CR2032 battery and implemented on a TI CC2640 microcontroller under TI RTOS. It acquires ECG at 400 Hz and performs real time artifact rejection using dynamic baseline matching and amplitude and frequency gating, followed by R peak detection and calculation of instantaneous heart rate and four time domain HRV metrics. Valid ECG segments and derived parameters are transmitted over secure BLE using ECC key exchange and AES 128 encryption, with dynamic transmit power control based on RSSI. Four power saving modes govern data transmission and sleep intervals, including event triggered modes that suppress artifact intervals and extend operating life to approximately 250 hours.</p>

<p>&nbsp;</p>

<p>Advantages: <br />
<br />
&bull; Provides continuous autonomous ECG monitoring with onboard analytics<br />
&bull; Improves signal fidelity using real time noise and motion artifact rejection<br />
&bull; Extends battery life through adaptive duty cycling and dynamic BLE power control<br />
&bull; Reduces data transmission volume by suppressing artifact segments<br />
&bull; Enhances security with ECC based key exchange and AES 128 encryption<br />
&bull; Improves comfort via a thin flexible two lead adhesive patch design<br />
&bull; Calculates HRV metrics on device to minimize external processing needs<br />
&bull; Supports low cost disposable deployment with simple coin cell power<br />
</p>

<p>&nbsp;</p>

<p>Applications: <br />
<br />
&bull; Remote patient monitoring<br />
&bull; Ambulatory arrhythmia detection<br />
&bull; Clinical research and drug safety trials<br />
&bull; Athlete training and recovery tracking<br />
&bull; Industrial worker health and safety monitoring<br />
</p>

<p>&nbsp;</p>

<p>Intellectual Property Summary: <br />
<br />
&bull; United States 11,883,176 - Issued 01/30/2024<br />
</p>

<p>&nbsp;</p>

<p>Stage of Development: <br />
Prototype validated under continuous monitoring conditions</p>

<p>&nbsp;</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>

<p>&nbsp;</p>

<p>Licensing Potential: <br />
Strong potential for adoption by medical device manufacturers, digital health platforms, and remote monitoring providers seeking low power, real time cardiac analytics in a comfortable, long duration wearable format.</p>

<p>&nbsp;</p>

<p>Additional Information: <br />
Prototype performance validation data and continuous monitoring results available upon request.</p>

<p>&nbsp;</p>

<p>Inventors:<br />
Kanad Ghose, Sandeep Mittal</p>]]></description><pubDate>Fri, 10 Apr 2026 13:33:58 GMT</pubDate><author>innovation@binghamton.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Smart_Low_Power_ECG_Patch_with_Integrated_Real_Time_Cardiac_Analytics</guid><dataField:caseId>RB628</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 13:36:08 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>This wearable ECG patch offers continuous heart monitoring while fixing common issues with current devices, such as bulky designs, short battery life, and missed data when signals are sent elsewhere for processing. By analyzing data directly on the device, it reduces power use and provides real-time heart rate, HRV, and irregular heartbeat information in a small, comfortable patch designed for long-term wear.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background>Ambulatory ECG monitoring systems often require bulky hardware, frequent battery changes, or off board signal processing that causes data gaps, missed alerts, and degraded signal fidelity. Noise, motion artifacts, and static transmission schemes further reduce reliability, while few devices integrate real time analytics with adaptive power management in a discreet, wearable patch.</dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology>This invention is a flexible two lead ECG patch powered by a CR2032 battery and implemented on a TI CC2640 microcontroller under TI RTOS. It acquires ECG at 400 Hz and performs real time artifact rejection using dynamic baseline matching and amplitude and frequency gating, followed by R peak detection and calculation of instantaneous heart rate and four time domain HRV metrics. Valid ECG segments and derived parameters are transmitted over secure BLE using ECC key exchange and AES 128 encryption, with dynamic transmit power control based on RSSI. Four power saving modes govern data transmission and sleep intervals, including event triggered modes that suppress artifact intervals and extend operating life to approximately 250 hours.</dataField:Technology><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[<br />
&bull; Provides continuous autonomous ECG monitoring with onboard analytics<br />
&bull; Improves signal fidelity using real time noise and motion artifact rejection<br />
&bull; Extends battery life through adaptive duty cycling and dynamic BLE power control<br />
&bull; Reduces data transmission volume by suppressing artifact segments<br />
&bull; Enhances security with ECC based key exchange and AES 128 encryption<br />
&bull; Improves comfort via a thin flexible two lead adhesive patch design<br />
&bull; Calculates HRV metrics on device to minimize external processing needs<br />
&bull; Supports low cost disposable deployment with simple coin cell power<br />]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[<br />
&bull; Remote patient monitoring<br />
&bull; Ambulatory arrhythmia detection<br />
&bull; Clinical research and drug safety trials<br />
&bull; Athlete training and recovery tracking<br />
&bull; Industrial worker health and safety monitoring<br />]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[<br />
&bull; United States 11,883,176 - Issued 01/30/2024<br />]]></dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>Prototype validated under continuous monitoring conditions</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential>Strong potential for adoption by medical device manufacturers, digital health platforms, and remote monitoring providers seeking low power, real time cardiac analytics in a comfortable, long duration wearable format.</dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo>Prototype performance validation data and continuous monitoring results available upon request.</dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Kanad</dataField:firstName><dataField:lastName>Ghose</dataField:lastName><dataField:title>Professor and Chair</dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>ghose@cs.binghamton.edu</dataField:emailAddress><dataField:phoneNumber>(607) 777-4608</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Sandeep</dataField:firstName><dataField:lastName>Mittal</dataField:lastName><dataField:title>Graduate Student</dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>smittal2@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>NSF I-Corps, XCEED, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jitendra</dataField:firstName><dataField:lastName>Jain</dataField:lastName><dataField:title>Director, Technology Transfer</dataField:title><dataField:department></dataField:department><dataField:emailAddress>jjain@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > Binghamton University| Technology Classifications| Technology Classifications > Medical Devices]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>AI-Driven Floor Plan Understanding for Indoor/Outdoor Navigation</title><link>https://canberra-ip.technologypublisher.com/tech?title=AI-Driven_Floor_Plan_Understanding_for_Indoor%2fOutdoor_Navigation</link><description><![CDATA[<p>This technology enables Vision Language Models to interpret raw floor plan images and generate accurate navigation plans without requiring structured digital maps. By combining visual and text-based reasoning, it allows robots and smart devices to understand spaces directly from images. The result is flexible, scalable navigation that works wherever a map image is available.</p>

<p>Background: <br />
Mobile robots and smart devices have difficulty using human-oriented floor plan images because these maps are not machine-readable and require extensive preprocessing. Existing systems depend on structured digital maps or environment-specific training, and they often fail to interpret complex spatial relationships or large open spaces. As a result, robots and assistive devices cannot reliably generate navigation plans directly from raw map images, limiting their usefulness in real-world environments.</p>

<p>Technology Overview: <br />
The invention applies Vision Language Models to parse floor plan images and produce navigation instructions from combined visual and textual prompts. A floor plan image and a task description containing start and goal locations are provided to the VLM, which generates a multi-step action sequence for reaching the goal. The approach achieves high accuracy on navigation tasks, performing especially well on small and moderately complex maps. It leverages commercially available VLMs such as GPT-4o and Claude 3.5 to reason over unstructured map images without specialized preprocessing.</p>

<p>Advantages: <br />
<br />
&bull; Enables VLMs to interpret raw floor plan images for navigation<br />
&bull; Achieves high accuracy in multi-step navigation tasks<br />
&bull; Integrates visual and textual reasoning for flexible task specification<br />
&bull; Eliminates dependency on structured or preprocessed digital maps<br />
&bull; Adapts to mobile robots and consumer devices without environment-specific training<br />
&bull; Improves accessibility by supporting natural language interaction<br />
&bull; Extends to robotics, urban planning, and emergency response use cases<br />
&bull; Provides a competitive advantage in autonomous indoor navigation systems<br />
</p>

<p>Applications: <br />
<br />
&bull; Mobile robotics navigation<br />
&bull; Smartphone-based indoor navigation<br />
&bull; Assistive navigation for visually impaired users<br />
&bull; Indoor/outdoor navigation in dynamic environments<br />
&bull; Emergency response planning<br />
&bull; Urban infrastructure mapping<br />
</p>

<p>Intellectual Property Summary: <br />
<br />
&bull; United States 63/884,317 Provisional Filed 09/18/2025 Status Filed<br />
</p>

<p>Stage of Development: <br />
Prototype</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>

<p>Licensing Potential: <br />
Strong potential for robotics developers, navigation software providers, and assistive technology companies seeking flexible, map-agnostic navigation solutions powered by AI-driven visual and language reasoning.</p>

<p>Additional Information: <br />
Additional technical details and evaluation results available upon request.</p>

<p>Inventors:<br />
Jeremy Blackburn, David DeFazio, Hrudayangam Mehta, Shiqi Zhang</p>]]></description><pubDate>Fri, 10 Apr 2026 13:33:46 GMT</pubDate><author>innovation@binghamton.edu</author><guid>https://canberra-ip.technologypublisher.com/tech?title=AI-Driven_Floor_Plan_Understanding_for_Indoor%2fOutdoor_Navigation</guid><dataField:caseId>RB769</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 13:37:36 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>This technology enables Vision Language Models to interpret raw floor plan images and generate accurate navigation plans without requiring structured digital maps. By combining visual and text-based reasoning, it allows robots and smart devices to understand spaces directly from images. The result is flexible, scalable navigation that works wherever a map image is available.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background>Mobile robots and smart devices have difficulty using human-oriented floor plan images because these maps are not machine-readable and require extensive preprocessing. Existing systems depend on structured digital maps or environment-specific training, and they often fail to interpret complex spatial relationships or large open spaces. As a result, robots and assistive devices cannot reliably generate navigation plans directly from raw map images, limiting their usefulness in real-world environments.</dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology>The invention applies Vision Language Models to parse floor plan images and produce navigation instructions from combined visual and textual prompts. A floor plan image and a task description containing start and goal locations are provided to the VLM, which generates a multi-step action sequence for reaching the goal. The approach achieves high accuracy on navigation tasks, performing especially well on small and moderately complex maps. It leverages commercially available VLMs such as GPT-4o and Claude 3.5 to reason over unstructured map images without specialized preprocessing.</dataField:Technology><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[<br />
&bull; Enables VLMs to interpret raw floor plan images for navigation<br />
&bull; Achieves high accuracy in multi-step navigation tasks<br />
&bull; Integrates visual and textual reasoning for flexible task specification<br />
&bull; Eliminates dependency on structured or preprocessed digital maps<br />
&bull; Adapts to mobile robots and consumer devices without environment-specific training<br />
&bull; Improves accessibility by supporting natural language interaction<br />
&bull; Extends to robotics, urban planning, and emergency response use cases<br />
&bull; Provides a competitive advantage in autonomous indoor navigation systems<br />]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[<br />
&bull; Mobile robotics navigation<br />
&bull; Smartphone-based indoor navigation<br />
&bull; Assistive navigation for visually impaired users<br />
&bull; Indoor/outdoor navigation in dynamic environments<br />
&bull; Emergency response planning<br />
&bull; Urban infrastructure mapping<br />]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[<br />
&bull; United States 63/884,317 Provisional Filed 09/18/2025 Status Filed<br />]]></dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>Prototype</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential>Strong potential for robotics developers, navigation software providers, and assistive technology companies seeking flexible, map-agnostic navigation solutions powered by AI-driven visual and language reasoning.</dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo>Additional technical details and evaluation results available upon request.</dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Shiqi</dataField:firstName><dataField:lastName>Zhang</dataField:lastName><dataField:title>Assistant Professor</dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>zhangs@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>David</dataField:firstName><dataField:lastName>DeFazio</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>ddefazi1@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Hrudayangam</dataField:firstName><dataField:lastName>Mehta</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>hmehta@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Jeremy</dataField:firstName><dataField:lastName>Blackburn</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>jblackbu@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Technologies, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Mehdi</dataField:firstName><dataField:lastName>Zadshir</dataField:lastName><dataField:title>Technology Transfer Manager</dataField:title><dataField:department></dataField:department><dataField:emailAddress>mzadshir@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > Binghamton University| Technology Classifications| Technology Classifications > Computers]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Privacy-Preserving Intelligent Search for Distributed Video Surveillance</title><link>https://canberra-ip.technologypublisher.com/tech/Privacy-Preserving_Intelligent_Search_for_Distributed_Video_Surveillance</link><description><![CDATA[<p>This technology lets users search surveillance video in real time using simple descriptions, solving the problem that current systems rely on sending large amounts of video or using biometric tools that are slow and raise privacy concerns. By processing data closer to where it is collected, the system delivers faster results, protects privacy, and uses much less network bandwidth.</p>

<p>&nbsp;</p>

<p>Background: <br />
Large-scale surveillance networks produce overwhelming volumes of video data that are difficult to analyze in real time, especially when operators have only general descriptions rather than precise identifiers. Centralized systems that transmit raw video create latency, scalability limits, and privacy concerns, while supervised biometric tools such as facial recognition are insufficient for vague queries and raise ethical issues. As a result, current systems struggle to provide efficient, privacy-preserving search capabilities for mission-critical environments.</p>

<p>&nbsp;</p>

<p>Technology Overview: <br />
The invention is an interactive surveillance system operating on an edge&ndash;fog&ndash;cloud architecture. Edge nodes perform human pose estimation to locate keypoints and crop body regions before extracting initial color features. Fog nodes receive only these features and apply clustering to determine dominant colors and map RGB centroids to human-readable labels through a predefined dictionary. Operators issue high-level queries such as clothing color, which are matched against extracted features to return relevant frames and camera IDs in under two seconds. The system uses a containerized microservices design for scalability and minimizes privacy risk by avoiding transmission of raw video.</p>

<p>&nbsp;</p>

<p>Advantages: <br />
<br />
&bull; Enables real time querying using high level semantic descriptions<br />
&bull; Preserves privacy by eliminating raw video transmission<br />
&bull; Reduces network load through edge based feature extraction<br />
&bull; Improves scalability with microservices architecture<br />
&bull; Delivers sub two second query response for mission critical use<br />
&bull; Operates effectively on low cost edge hardware<br />
&bull; Supports decentralized processing for system resilience<br />
&bull; Allows flexible searching without biometric identifiers<br />
</p>

<p>&nbsp;</p>

<p>Applications: <br />
<br />
&bull; Public infrastructure security<br />
&bull; Private facility security and loss prevention<br />
&bull; Emergency search and rescue<br />
&bull; Smart city forensic search<br />
&bull; Industrial safety monitoring<br />
</p>

<p>&nbsp;</p>

<p>Intellectual Property Summary: <br />
<br />
&bull; United States 12,211,277 - Issued 01/28/2025<br />
</p>

<p>&nbsp;</p>

<p>Stage of Development: <br />
Prototype</p>

<p>&nbsp;</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>

<p>&nbsp;</p>

<p>Licensing Potential: <br />
Strong potential for adoption by security system providers, smart city developers, and infrastructure operators seeking real-time, privacy-preserving video analytics with reduced bandwidth and scalable edge deployment for mission-critical environments.</p>

<p>&nbsp;</p>

<p>Additional Information: <br />
Prototype system demonstrations and performance validation details available upon request.</p>

<p>&nbsp;</p>

<p>Inventors:<br />
Yu Chen, Seyed yahya Nikouei</p>]]></description><pubDate>Fri, 10 Apr 2026 13:24:10 GMT</pubDate><author>innovation@binghamton.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Privacy-Preserving_Intelligent_Search_for_Distributed_Video_Surveillance</guid><dataField:caseId>RB640</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 13:29:25 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>This technology lets users search surveillance video in real time using simple descriptions, solving the problem that current systems rely on sending large amounts of video or using biometric tools that are slow and raise privacy concerns. By processing data closer to where it is collected, the system delivers faster results, protects privacy, and uses much less network bandwidth.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background>Large-scale surveillance networks produce overwhelming volumes of video data that are difficult to analyze in real time, especially when operators have only general descriptions rather than precise identifiers. Centralized systems that transmit raw video create latency, scalability limits, and privacy concerns, while supervised biometric tools such as facial recognition are insufficient for vague queries and raise ethical issues. As a result, current systems struggle to provide efficient, privacy-preserving search capabilities for mission-critical environments.</dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology><![CDATA[The invention is an interactive surveillance system operating on an edge&ndash;fog&ndash;cloud architecture. Edge nodes perform human pose estimation to locate keypoints and crop body regions before extracting initial color features. Fog nodes receive only these features and apply clustering to determine dominant colors and map RGB centroids to human-readable labels through a predefined dictionary. Operators issue high-level queries such as clothing color, which are matched against extracted features to return relevant frames and camera IDs in under two seconds. The system uses a containerized microservices design for scalability and minimizes privacy risk by avoiding transmission of raw video.]]></dataField:Technology><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[<br />
&bull; Enables real time querying using high level semantic descriptions<br />
&bull; Preserves privacy by eliminating raw video transmission<br />
&bull; Reduces network load through edge based feature extraction<br />
&bull; Improves scalability with microservices architecture<br />
&bull; Delivers sub two second query response for mission critical use<br />
&bull; Operates effectively on low cost edge hardware<br />
&bull; Supports decentralized processing for system resilience<br />
&bull; Allows flexible searching without biometric identifiers<br />]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[<br />
&bull; Public infrastructure security<br />
&bull; Private facility security and loss prevention<br />
&bull; Emergency search and rescue<br />
&bull; Smart city forensic search<br />
&bull; Industrial safety monitoring<br />]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[<br />
&bull; United States 12,211,277 - Issued 01/28/2025<br />]]></dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>Prototype</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential>Strong potential for adoption by security system providers, smart city developers, and infrastructure operators seeking real-time, privacy-preserving video analytics with reduced bandwidth and scalable edge deployment for mission-critical environments.</dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo>Prototype system demonstrations and performance validation details available upon request.</dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Yu</dataField:firstName><dataField:lastName>Chen</dataField:lastName><dataField:title>Professor</dataField:title><dataField:department><![CDATA[Electrical & Computer Engineering]]></dataField:department><dataField:emailAddress>ychen@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Seyed yahya</dataField:firstName><dataField:lastName>Nikouei</dataField:lastName><dataField:title></dataField:title><dataField:department>Electrical and Computer Engineering</dataField:department><dataField:emailAddress>snikoue1@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Matthew</dataField:firstName><dataField:lastName>Quimby</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>mquimby1@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > Binghamton University| Technology Classifications| Technology Classifications > Engineering]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Adaptive 360-degree Real-time Video Communication System</title><link>https://canberra-ip.technologypublisher.com/tech/Adaptive_360-degree_Real-time_Video_Communication_System</link><description><![CDATA[<p>This technology enables high-quality real-time 360-degree video communication by adapting video content to each user&rsquo;s viewport. By concentrating resolution where the user is actually looking, it reduces bandwidth waste and improves visual clarity under tight latency constraints. The result is an efficient, immersive communication experience optimized for real-time interaction while maintaining performance across varying network conditions.</p>

<p>Background: <br />
Real-time 360-degree video communication requires transmitting full spherical video frames even though users view only a small portion at any moment, wasting bandwidth and degrading viewport quality. Low-latency requirements prevent the use of buffering, complex prediction models, or heavy processing borrowed from on-demand streaming, and existing real-time communication frameworks are not designed to optimize 360-degree content. This leads to inefficient transmission, poor visual fidelity in the user&rsquo;s field of view, and difficulty meeting real-time performance constraints.</p>

<p>Technology Overview: <br />
The invention uses content-adaptive oriented projection techniques to dynamically reshape 360-degree video frames so that pixel density is concentrated in a user&rsquo;s current viewing direction. Real-time viewport feedback and network conditions determine projection parameters, which are applied using GPU-accelerated transformations for low-latency processing. Projection metadata is transmitted using RTP header extensions, allowing receivers to accurately reverse the transformation and display high-quality viewport content while minimizing transmission of unviewed pixels.</p>

<p>Advantages: <br />
<br />
&bull; Improves viewport visual quality through dynamic projection<br />
&bull; Reduces bandwidth consumption by minimizing unviewed pixel transmission<br />
&bull; Achieves real-time performance using GPU-accelerated transformations<br />
&bull; Integrates seamlessly with existing WebRTC workflows<br />
&bull; Enhances user experience with adaptive content and bitrate control<br />
</p>

<p>Applications: <br />
<br />
&bull; Immersive video conferencing<br />
&bull; Industrial telepresence and remote inspection<br />
&bull; Real-time medical telementoring<br />
&bull; Interactive immersive content delivery<br />
</p>

<p>Intellectual Property Summary: <br />
<br />
&bull; United States &ndash; 63/090,273 &ndash; Provisional &ndash; Filed 10/11/2020 &ndash; Issued 10/12/2020 &ndash; Status: Converted<br />
&bull; United States &ndash; 17/449,893 &ndash; US20220116441A1 &ndash; Patent No. 11,785,069 &ndash; Utility &ndash; Filed 10/4/2021 &ndash; Issued 10/10/2023 &ndash; Status: Patented<br />
</p>

<p>Stage of Development: <br />
Prototype</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>

<p>Licensing Potential: <br />
Strong potential for adoption by video communication platforms, immersive media providers, and telepresence solution developers seeking bandwidth-efficient, low-latency, and high-quality 360-degree streaming technologies.</p>

<p>Additional Information: <br />
Additional technical details and implementation information available upon request.</p>

<p>Inventors:<br />
Yao Liu, Shuoqian Wang</p>]]></description><pubDate>Fri, 10 Apr 2026 13:21:51 GMT</pubDate><author>innovation@binghamton.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Adaptive_360-degree_Real-time_Video_Communication_System</guid><dataField:caseId>RB645</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 13:25:19 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary><![CDATA[This technology enables high-quality real-time 360-degree video communication by adapting video content to each user&rsquo;s viewport. By concentrating resolution where the user is actually looking, it reduces bandwidth waste and improves visual clarity under tight latency constraints. The result is an efficient, immersive communication experience optimized for real-time interaction while maintaining performance across varying network conditions.]]></dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background><![CDATA[Real-time 360-degree video communication requires transmitting full spherical video frames even though users view only a small portion at any moment, wasting bandwidth and degrading viewport quality. Low-latency requirements prevent the use of buffering, complex prediction models, or heavy processing borrowed from on-demand streaming, and existing real-time communication frameworks are not designed to optimize 360-degree content. This leads to inefficient transmission, poor visual fidelity in the user&rsquo;s field of view, and difficulty meeting real-time performance constraints.]]></dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology><![CDATA[The invention uses content-adaptive oriented projection techniques to dynamically reshape 360-degree video frames so that pixel density is concentrated in a user&rsquo;s current viewing direction. Real-time viewport feedback and network conditions determine projection parameters, which are applied using GPU-accelerated transformations for low-latency processing. Projection metadata is transmitted using RTP header extensions, allowing receivers to accurately reverse the transformation and display high-quality viewport content while minimizing transmission of unviewed pixels.]]></dataField:Technology><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[<br />
&bull; Improves viewport visual quality through dynamic projection<br />
&bull; Reduces bandwidth consumption by minimizing unviewed pixel transmission<br />
&bull; Achieves real-time performance using GPU-accelerated transformations<br />
&bull; Integrates seamlessly with existing WebRTC workflows<br />
&bull; Enhances user experience with adaptive content and bitrate control<br />]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[<br />
&bull; Immersive video conferencing<br />
&bull; Industrial telepresence and remote inspection<br />
&bull; Real-time medical telementoring<br />
&bull; Interactive immersive content delivery<br />]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[<br />
&bull; United States &ndash; 63/090,273 &ndash; Provisional &ndash; Filed 10/11/2020 &ndash; Issued 10/12/2020 &ndash; Status: Converted<br />
&bull; United States &ndash; 17/449,893 &ndash; US20220116441A1 &ndash; Patent No. 11,785,069 &ndash; Utility &ndash; Filed 10/4/2021 &ndash; Issued 10/10/2023 &ndash; Status: Patented<br />]]></dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>Prototype</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential>Strong potential for adoption by video communication platforms, immersive media providers, and telepresence solution developers seeking bandwidth-efficient, low-latency, and high-quality 360-degree streaming technologies.</dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo>Additional technical details and implementation information available upon request.</dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Shuoqian</dataField:firstName><dataField:lastName>Wang</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>swang130@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Yao</dataField:firstName><dataField:lastName>Liu</dataField:lastName><dataField:title></dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>yaoliu@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Technologies, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jitendra</dataField:firstName><dataField:lastName>Jain</dataField:lastName><dataField:title>Director, Technology Transfer</dataField:title><dataField:department></dataField:department><dataField:emailAddress>jjain@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > Binghamton University| Technology Classifications > Computers]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Ultra-Efficient Encoded ECG System for Real-Time Arrhythmia Detection</title><link>https://canberra-ip.technologypublisher.com/tech/Ultra-Efficient_Encoded_ECG_System_for_Real-Time_Arrhythmia_Detection</link><description><![CDATA[<p>This technology enables real-time arrhythmia detection using a wearable ECG patch, solving a key problem with current devices that must transmit large amounts of raw heart data, which quickly drains battery life. By sending only compact, encoded features instead of full waveforms, it drastically reduces data volume and power use, supporting long-term continuous monitoring on small, battery-powered devices.</p>

<p>Background: <br />
Continuous arrhythmia monitoring with wearable ECG sensors is limited by the large data volumes required to transmit raw or compressed waveforms, which consume significant power and shorten device lifespan. Battery-powered wearables struggle to support long-term operation because frequent recharging interrupts monitoring, reduces compliance, and burdens users. Existing compression techniques still demand substantial computation or sacrifice diagnostic detail, making it difficult to achieve reliable real-time detection under tight energy and bandwidth constraints.</p>

<p>Technology Overview: <br />
The invention uses a Smart ECG Patch that acquires ECG signals, detects R-peaks, removes artifacts, and encodes each cardiac cycle into 14 integer parameters representing QRS morphology and instantaneous heart rate. This compact representation is transmitted via low-power Bluetooth to a host device, where a BiLSTM-based classifier performs real-time arrhythmia detection across seven categories. The system incorporates adaptive power management and secure transmission using ECC cryptography and AES-128 encryption, enabling efficient, continuous monitoring.</p>

<p>Advantages: <br />
<br />
&bull; Reduces data transmission through compact ECG feature encoding<br />
&bull; Extends battery life by minimizing wireless communication demands<br />
&bull; Supports real-time arrhythmia detection using a lightweight encoded signal<br />
&bull; Lowers computational load on wearable hardware<br />
&bull; Maintains diagnostic accuracy using a BiLSTM classifier trained on encoded features<br />
&bull; Enables efficient continuous monitoring on small, battery-powered devices<br />
</p>

<p>Applications: <br />
<br />
&bull; Remote cardiac monitoring<br />
&bull; Wearable health and fitness tracking<br />
&bull; Military physiological monitoring<br />
&bull; First-responder physiological monitoring<br />
&bull; Athletic performance tracking<br />
&bull; Recovery tracking<br />
</p>

<p>Intellectual Property Summary: <br />
<br />
&bull; United States US 2024-0188876 &ndash; Pending<br />
</p>

<p>Stage of Development: <br />
Prototype demonstrated under continuous monitoring conditions</p>

<p>Licensing Status: <br />
This technology is available for licensing.</p>

<p>Licensing Potential: <br />
Strong potential for wearable medical device manufacturers, digital health platforms, and remote patient monitoring providers seeking energy-efficient, real-time cardiac monitoring solutions with extended battery life and reduced data transmission requirements.</p>

<p>Additional Information: <br />
Information available upon request.</p>

<p>Inventors:<br />
Kanad Ghose, Sandeep Mittal</p>

<p>&nbsp;</p>]]></description><pubDate>Fri, 10 Apr 2026 13:10:13 GMT</pubDate><author>innovation@binghamton.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Ultra-Efficient_Encoded_ECG_System_for_Real-Time_Arrhythmia_Detection</guid><dataField:caseId>RB654</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 13:16:43 GMT</dataField:lastUpdateDate><dataField:AlgoliaSummary>This technology enables real-time arrhythmia detection using a wearable ECG patch, solving a key problem with current devices that must transmit large amounts of raw heart data, which quickly drains battery life. By sending only compact, encoded features instead of full waveforms, it drastically reduces data volume and power use, supporting long-term continuous monitoring on small, battery-powered devices.</dataField:AlgoliaSummary><dataField:HDBackground>Background:</dataField:HDBackground><dataField:Background>Continuous arrhythmia monitoring with wearable ECG sensors is limited by the large data volumes required to transmit raw or compressed waveforms, which consume significant power and shorten device lifespan. Battery-powered wearables struggle to support long-term operation because frequent recharging interrupts monitoring, reduces compliance, and burdens users. Existing compression techniques still demand substantial computation or sacrifice diagnostic detail, making it difficult to achieve reliable real-time detection under tight energy and bandwidth constraints.</dataField:Background><dataField:HDTechnology>Technology Overview:</dataField:HDTechnology><dataField:Technology>The invention uses a Smart ECG Patch that acquires ECG signals, detects R-peaks, removes artifacts, and encodes each cardiac cycle into 14 integer parameters representing QRS morphology and instantaneous heart rate. This compact representation is transmitted via low-power Bluetooth to a host device, where a BiLSTM-based classifier performs real-time arrhythmia detection across seven categories. The system incorporates adaptive power management and secure transmission using ECC cryptography and AES-128 encryption, enabling efficient, continuous monitoring.</dataField:Technology><dataField:HDAdvantages>Advantages:</dataField:HDAdvantages><dataField:Advantages><![CDATA[<br />
&bull; Reduces data transmission through compact ECG feature encoding<br />
&bull; Extends battery life by minimizing wireless communication demands<br />
&bull; Supports real-time arrhythmia detection using a lightweight encoded signal<br />
&bull; Lowers computational load on wearable hardware<br />
&bull; Maintains diagnostic accuracy using a BiLSTM classifier trained on encoded features<br />
&bull; Enables efficient continuous monitoring on small, battery-powered devices<br />]]></dataField:Advantages><dataField:HDApplication>Applications:</dataField:HDApplication><dataField:Application><![CDATA[<br />
&bull; Remote cardiac monitoring<br />
&bull; Wearable health and fitness tracking<br />
&bull; Military physiological monitoring<br />
&bull; First-responder physiological monitoring<br />
&bull; Athletic performance tracking<br />
&bull; Recovery tracking<br />]]></dataField:Application><dataField:HDPatentStatus>Intellectual Property Summary:</dataField:HDPatentStatus><dataField:PatentStatus><![CDATA[<br />
&bull; United States US 2024-0188876 &ndash; Pending<br />]]></dataField:PatentStatus><dataField:HDStageOfDevelopment>Stage of Development:</dataField:HDStageOfDevelopment><dataField:StageOfDevelopment>Prototype demonstrated under continuous monitoring conditions</dataField:StageOfDevelopment><dataField:HDLicensingStatus>Licensing Status:</dataField:HDLicensingStatus><dataField:LicensingStatus>This technology is available for licensing.</dataField:LicensingStatus><dataField:HDLicensingPotential>Licensing Potential:</dataField:HDLicensingPotential><dataField:LicensingPotential>Strong potential for wearable medical device manufacturers, digital health platforms, and remote patient monitoring providers seeking energy-efficient, real-time cardiac monitoring solutions with extended battery life and reduced data transmission requirements.</dataField:LicensingPotential><dataField:HDAdditionalInfo>Additional Information:</dataField:HDAdditionalInfo><dataField:AdditionalInfo>Information available upon request.</dataField:AdditionalInfo><dataField:inventorList><dataField:inventor><dataField:firstName>Kanad</dataField:firstName><dataField:lastName>Ghose</dataField:lastName><dataField:title>Professor and Chair</dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>ghose@cs.binghamton.edu</dataField:emailAddress><dataField:phoneNumber>(607) 777-4608</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Sandeep</dataField:firstName><dataField:lastName>Mittal</dataField:lastName><dataField:title>Graduate Student</dataField:title><dataField:department>Computer Science</dataField:department><dataField:emailAddress>smittal2@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Technologies, XCEED, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jitendra</dataField:firstName><dataField:lastName>Jain</dataField:lastName><dataField:title>Director, Technology Transfer</dataField:title><dataField:department></dataField:department><dataField:emailAddress>jjain@binghamton.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Campus > Binghamton University| Technology Classifications > Healthcare IT]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Heart Rate-Based PTSD Classification System</title><link>https://canberra-ip.technologypublisher.com/tech/Heart_Rate-Based_PTSD_Classification_System</link><description><![CDATA[<h4>Application</h4>

<p>This technology delivers an objective, data‑driven PTSD assessment based on heart activity, addressing the absence of standardized physiological criteria and reducing dependence on subjective self‑reports.</p>

<h4>Key Benefits</h4>

<ul>
	<li>Uses measurable physiological signals rather than self-reported symptoms.</li>
	<li>Employs non-invasive electrocardiography or wearable sensors for heart activity data collection.</li>
	<li>Machine learning-based classifier enhances diagnostic reliability and long-term monitoring of illness severity.</li>
</ul>

<h4>Market Summary</h4>

<p>PTSD affects millions of individuals globally, with particularly high prevalence among military and veteran populations and a significant presence in the broader public. Despite its impact, PTSD diagnosis and ongoing assessment still rely largely on subjective self-reporting and clinical judgment, increasing the risk of missed or inaccurate diagnoses and suboptimal care. As healthcare delivery expands across clinical, military, and virtual environments, there is growing demand for objective, scalable solutions that support accurate screening and continuous monitoring. Tools that deliver reliable physiological insights can enable earlier identification, support personalized treatment decisions, and ultimately improve long-term outcomes for individuals living with PTSD.</p>

<h4>Technical Summary</h4>

<p>Emory researchers have developed a system utilizing a novel heart rate-based window segmentation strategy that analyzes RR interval data &mdash; the time between two consecutive R-waves &mdash; on an electrocardiogram (ECG) from electrocardiography or similar heart activity measurements. It identifies quiescent segments of RR intervals to extract heart rate variability (HRV) features, which reflects overall variability in heartbeats and autonomic nervous system function. These features are compared against a machine learning classifier trained on data from individuals with and without PTSD, enabling determination of PTSD status or severity.</p>

<h4>Development Stage</h4>

<p>Validated using ECG recordings from human subjects.</p>

<p><strong>Publication</strong> Reinertsen, E., et al. (2017). Heart rate-based window segmentation improves accuracy of classifying posttraumatic stress disorder using heart rate variability measures. <em>Physiological Measurement</em>, 38(6), 1061&ndash;1076. https://doi.org/10.1088/1361-6579/aa6e9c</p>]]></description><pubDate>Fri, 10 Apr 2026 12:15:37 GMT</pubDate><author>emoryott@inteummail.com</author><guid>https://canberra-ip.technologypublisher.com/tech/Heart_Rate-Based_PTSD_Classification_System</guid><dataField:caseId>17042</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 12:15:37 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Gari</dataField:firstName><dataField:lastName>Clifford</dataField:lastName><dataField:title><![CDATA[Professor & Chair]]></dataField:title><dataField:department>SOM: BMI: Admin</dataField:department><dataField:emailAddress>gari@dbmi.emory.edu</dataField:emailAddress><dataField:phoneNumber>404-712-0163</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Erik</dataField:firstName><dataField:lastName>Reinertsen</dataField:lastName><dataField:title>PhD Student; Research Fellow/Trainee</dataField:title><dataField:department>SOM: Biomedical Engineering</dataField:department><dataField:emailAddress>erikrtn@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Amit J.</dataField:firstName><dataField:lastName>Shah</dataField:lastName><dataField:title>Associate Professor</dataField:title><dataField:department>SPH: Epidemiology</dataField:department><dataField:emailAddress>ajshah3@emory.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Shamim</dataField:firstName><dataField:lastName>Nemati</dataField:lastName><dataField:title>Adjunct Assistant Professor, Biomedical Informatics</dataField:title><dataField:department>SOM: BMI: Admin</dataField:department><dataField:emailAddress>snemati@health.ucsd.edu</dataField:emailAddress><dataField:phoneNumber>405-850-4751</dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords>Algorithm, AI, and Machine Learning, Cardiovascular Treatments, Non-Therapeutics, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Shweta</dataField:firstName><dataField:lastName>Ghai</dataField:lastName><dataField:title>Licensing Associate</dataField:title><dataField:department>Office Of Technology Transfer</dataField:department><dataField:emailAddress>shweta.ghai@emory.edu</dataField:emailAddress><dataField:phoneNumber>404-785-9340</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[TechPub Algolia > Diagnostics]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters><![CDATA[<link rel=“canonical” href=”https://emoryott.technologypublisher.com/techcase/17042 />

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<p>Example: The National Cancer Institute (NCI) seeks research co-development partners and/or licensees for a collection of T-cell receptors (TCRs) that specifically target the mutated KRAS antigen.</p>

<p>This technology encompasses a DNA methylation&ndash;based diagnostic platform designed to improve the accuracy and consistency of cancer classification, with demonstrated utility for tumors of the central nervous system, kidney, and hematopoietic system. By identifying disease-specific methylation signatures, the approach reduces interobserver variability and enhances diagnostic confidence. The central nervous system (CNS) classifier is built from a curated reference set of 16,567 methylation profiles and organizes tumors into 22 families and 133 clinically relevant diagnostic classes, including 21 newly developed methylation classes not represented in other existing tools. Across multiple independent validation cohorts (n = 5,875), the classifier demonstrated robust performance, and in a clinical-impact analysis of 1,204 NIH validation cases, methylation profiling materially influenced final diagnosis in 74.4% of cases by refining, increasing precision, or reclassifying. The CNS classifier was deployed as a user-facing software tool, MethylScape Analysis, which streamlines methylation-based classification workflows for CNS tumors (https://methylscape.ccr.cancer.gov/). The development of multiple specialized classifiers supports a more granular understanding of tumor biology and&nbsp; informed clinical decision-making.</p>

<h2>Description of Technology:</h2>

<p>Accurate CNS tumor classification can be challenging when tumors show overlapping histology, limited tissue or atypical features. A meaningful fraction of cases remains unclassified or assigned with limited confidence with current molecular tools. These diagnostic ambiguities directly affect subtype and grade assignment which, in turn, influence treatment planning, prognosis, and clinical trial eligibility. Variability across observers and institutions can lead to additional testing, delays, and inconsistent diagnoses.</p>

<p>The NCI/Bethesda classifier addresses this gap using DNA methylation patterns as a robust molecular fingerprint. It applies a stratified machine learning framework to extend diagnostic coverage and improve assignment confidence for CNS tumors. The classifier was developed from a rigorously curated reference set of over 16k methylation profiles, structured into 22 tumor families and 133 clinically relevant diagnostic classes and includes 21 recently developed methylation classes not represented in existing tools. The approach has been validated across multiple independent cohorts (n = 5,875) and supports deployment through MethylScape, a public web-based portal that streamlines classifier execution for broad accessibility. In an NIH validation cohort analysis of 1,204 high-confidence matches with pre-methylation diagnoses available, methylation profiling confirmed the initial diagnosis in 25.6% of cases while driving clinically meaningful diagnostic evolution in the remainder, including refined diagnosis (subtyping) in 14.6%, new diagnosis with increased precision in 54.7%, and substantial diagnostic reclassification in 5.0%&mdash;changes that are expected to affect patient management in the reclassification subset.</p>

<p>Renal neoplasms present a parallel diagnostic challenge due to morphologic and molecular heterogeneity, overlapping microscopic features, and interobserver variability. As a result, a subset of cases are unclassifiable even after immunohistochemical, mutation and cytogenetic workups. To address this, the Kidney Classifier component of this platform leverages genome-wide DNA methylation profiling (feasible on formalin-fixed paraffin-embedded tissue using robust array-based methods). It was developed through examination of methylation signatures from over 2,000 renal neoplasms, identifying 23 coherent methylation groups that correlate with known tumor types and reveal clinically relevant novel subtypes. A machine learning classifier trained on 1,284 samples was externally tested on 287 renal neoplasms, demonstrating &gt;90% concordance between expected neoplasm type and high-score methylation-based classification, with discordant cases highlighting opportunities for diagnostic reclassification and improved precision in challenging renal tumor evaluations.</p>

<p>Licensing and collaboration opportunities include commercial development of methylation-based diagnostic tests and/or software-enabled classification solutions for clinical laboratories, reference labs, and diagnostic companies. Partners may engage in external validation (retrospective and prospective), assay standardization, integration into pathology workflows and reporting systems, and extension of classifier coverage to additional tumor types and multi-institutional datasets. Consistent with consensus recommendations for complementary classifiers, the inventors are also interested in collaborations that: (1) operationalize multi-classifier strategies (concordant/complementary prediction to increase confidence; (2) leverage discordance to trigger orthogonal follow-up) and (3) accelerate clinical translation through scalable deployment models- including CLIA laboratory workflows and regulated diagnostic pathways.</p>

<h2>Potential Commercial Applications:</h2>

<ul>
	<li>Molecular classification and diagnosis of CNS and kidney tumors, including difficult-to-classify and low-confidence cases</li>
	<li>Diagnostic subtyping aligned to WHO-guided entities</li>
	<li>Reference-lab and hospital-lab deployment</li>
	<li>Clinical trial stratification and translational research cohort harmonization</li>
	<li>Multi-classifier diagnostic decision support</li>
	<li>Cancer treatment development</li>
</ul>

<h2>Competitive Advantages:</h2>

<ul>
	<li>Developed from a rigorously curated, large reference set of methylation profiles</li>
	<li>Clinically relevant CNS diagnostic</li>
	<li>CNS tumor methylation classes not represented in existing tools, expanding diagnostic coverage</li>
	<li>Clinical-impact analysis creating superior diagnostic precision</li>
	<li>Superior classifier for kidney cancer</li>
	<li>Superior classifiers for multiple solid, difficult-to-diagnose tumors</li>
	<li>Integrative into clinical workflows, improving diagnostic practices and enhancing patient care</li>
</ul>]]></description><pubDate>Fri, 10 Apr 2026 11:34:38 GMT</pubDate><author>nihott@nih.gov</author><guid>https://canberra-ip.technologypublisher.com/tech/DNA_Methylation-Based_Cancer_Diagnostics_for_Accurate_Tumor_Classification</guid><dataField:caseId>TAB-5088</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 11:34:38 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Kenneth</dataField:firstName><dataField:lastName>Aldape</dataField:lastName><dataField:title>Chief, Senior Investigator</dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Ziedulla</dataField:firstName><dataField:lastName>Abdullaev</dataField:lastName><dataField:title>Scientist Contractor</dataField:title><dataField:department>DIR</dataField:department><dataField:emailAddress>zabdullaev@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>301-594-2221</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Rustamzhon</dataField:firstName><dataField:lastName>Turakulov</dataField:lastName><dataField:title>Bioinformatic Scientist (contractor)</dataField:title><dataField:department></dataField:department><dataField:emailAddress>rust.turakulov@nih.gov</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Stefania</dataField:firstName><dataField:lastName>Pittaluga</dataField:lastName><dataField:title>Staff Clinician</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>stefpitt@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>301-480-8465</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Mark</dataField:firstName><dataField:lastName>Raffeld</dataField:lastName><dataField:title>Head, Diagnostics Core and Staff Clinician</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>mraff@box-m.nih.gov</dataField:emailAddress><dataField:phoneNumber>301-480-8927</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Elaine</dataField:firstName><dataField:lastName>Jaffe</dataField:lastName><dataField:title>Head, Hematopathology Section</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>elainejaffe@nih.gov</dataField:emailAddress><dataField:phoneNumber>301-480-8040</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Omkar</dataField:firstName><dataField:lastName>Singh</dataField:lastName><dataField:title>Postdoctoral Fellow</dataField:title><dataField:department></dataField:department><dataField:emailAddress>omkar.singh@nih.gov</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Antonios</dataField:firstName><dataField:lastName>Papanicolau-Sengos</dataField:lastName><dataField:title>Staff Clinician</dataField:title><dataField:department></dataField:department><dataField:emailAddress>antonios.papanicolau-sengos@nih.gov</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Jaime</dataField:firstName><dataField:lastName>Greene</dataField:lastName><dataField:title>Technology Licensing Specialist</dataField:title><dataField:department></dataField:department><dataField:emailAddress>greenejaime@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>240-276-6633</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Application > Diagnostics| TherapeuticArea > Oncology| Collaboration Sought > Collaboration| Collaboration Sought > Licensing]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Advanced Pulsed-Laser Synthesis for Metal Carbides</title><link>https://canberra-ip.technologypublisher.com/tech/Advanced_Pulsed-Laser_Synthesis_for_Metal_Carbides</link><description><![CDATA[<p ><strong>NU 2025-190</strong></p>

<p ><strong>SHORT DESCRIPTION</strong><br />
A pulsed-laser synthesis method for making advanced metastable materials, including metal carbides and nitrides.</p>


	
		
			<strong>INVENTORS</strong>

			<ul >
				<li>Bryan Hunter*</li>
				<li>Alexis Magana</li>
				<li>Christopher Nowak</li>
			</ul>
			 <em>* Principal Investigator</em>
			
			<p><strong>NU 2025-190</strong></p>

			<p><strong>IP STATUS</strong></p>

			<p>Provisional Application Filed (joint with Harvard University)</p>

			<p><strong>DEVELOPMENT STAGE</strong></p>

			<p>TRL-3 - Experimental Proof-of-Concept: Active R&amp;D is initiated and key functions have been validated in a lab environment.</p>
			
		
	


<p><img alt="" src="https://nulive.technologypublisher.com/files/sites/lead_carbide_redo.png"  /></p>

<p ><strong>BACKGROUND</strong><br />
Metal carbides are a broad class of compounds containing metal-carbon bonds, endowing them with extreme durability, high melting points, and unique electronic properties that make them amenable to a variety of technological applications. Carbides are often employed at extreme temperatures and pressures for this reason. Despite their value, carbide synthesis presents many challenges, and certain metals do not form well-defined carbides at all.&nbsp;Current synthesis methods rarely yield new binary compounds, especially for metals like lead that poorly dissolve carbon. Conventional high-temperature and chemical protocols often require extreme conditions and incur high costs. There remains a need for innovative processes capable of producing advanced refractory materials.<br />
&nbsp;</p>

<p ><strong>ABSTRACT</strong><br />
Northwestern researchers report the synthesis of lead(II) carbide (Pb<sub>2</sub>C) using pulsed-laser synthesis (PuLS) in an unsaturated liquid hydrocarbon. PuLS accesses the &ldquo;impossible carbide&rdquo; by reaching extreme temperatures and pressures. Lead(II) carbide was characterized as a layered, hexagonal methide with paramagnetic behavior at room temperature using microscopy and spectroscopy. This technology enables further exploration of previously inaccessible compounds and opens new avenues for discovering novel carbides with unique structural and electronic properties.</p>

<p ><strong>APPLICATIONS</strong></p>

<ul >
	<li>Synthesis of many metastable materials, including nitrides and carbides (difficult to manufacture)</li>
	<li>Lead&nbsp;carbide&nbsp;in&nbsp;itself&nbsp;has&nbsp;not&nbsp;been&nbsp;explored&nbsp;(e.g. magnetic properties/superconductivity),&nbsp;though&nbsp;other&nbsp;lead&nbsp;compounds&nbsp;have&nbsp;seen&nbsp;huge&nbsp;utility&nbsp;(e.g. perovskites)&nbsp;</li>
	<li>Potential applications in high-temperature components, catalytic reactors, electronic contacts, and optical coatings</li>
</ul>

<p ><strong>ADVANTAGES</strong></p>

<ul >
	<li>Provides a general&nbsp;method to produce nanoparticles of unique composition and structure (PuLS)&nbsp;</li>
	<li>Produces metastable materials</li>
	<li>Uses a new flow-through&nbsp;technology&nbsp;that maximizes&nbsp;product&nbsp;formation</li>
</ul>

<p ><strong>CATEGORY/INDUSTRY PIPELINE</strong><br />
Materials and Industrial Processes; Engineering &amp; Technology</p>

<p ><strong>KEYWORDS</strong><br />
pulsed-laser synthesis,&nbsp;lead carbide,&nbsp;refractory materials, high-temperature synthesis, nanomaterials, metal carbides</p>

<p ><strong>INVO CONTACT&nbsp;</strong></p>

<p><a href="https://www.invo.northwestern.edu/about/our-team/anne-isabelle-henry-phd.html" target="_blank"><strong>Anne-Isabelle Henry Baruch, PhD</strong></a></p>

<p>Senior Invention Manager</p>

<p>(847) 491-4629</p>

<p><a href="mailto:a-henry@northwestern.edu" target="_blank">a-henry@northwestern.edu</a></p>]]></description><pubDate>Fri, 10 Apr 2026 10:37:10 GMT</pubDate><author>dragos@northwestern.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Advanced_Pulsed-Laser_Synthesis_for_Metal_Carbides</guid><dataField:caseId>2025-190</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 10:38:04 GMT</dataField:lastUpdateDate><dataField:inventorList></dataField:inventorList><dataField:keywords>Materials, Metals, Nanoparticle, </dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Anne-Isabelle</dataField:firstName><dataField:lastName>Baruch</dataField:lastName><dataField:title>Senior Invention Manager</dataField:title><dataField:department>Innovation and New Ventures</dataField:department><dataField:emailAddress>a-henry@northwestern.edu</dataField:emailAddress><dataField:phoneNumber>847/491-2952</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Physical Sciences > Materials and Industrial Processes]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Modular Scanning Probe Microscopy (SPM) Head and Compact UHV Probe Transfer System</title><link>https://canberra-ip.technologypublisher.com/tech/Modular_Scanning_Probe_Microscopy_(SPM)_Head_and_Compact_UHV_Probe_Transfer_System</link><description><![CDATA[<p ></p>

<p >​<img src="https://rutgers.technologypublisher.com/files/sites/mp-2025-010p_image-20260410103603-1.png"  /><img src="https://rutgers.technologypublisher.com/files/sites/image1946.png"  /></p>

<p >Connection of STM head to transfer mechanism in RT chamber</p>

<p ></p>

<p ><br />
<strong>Invention Summary:</strong> </p>

<p ></p>

<p >Traditional scanning probe microscopy (SPM) systems face a range of significant technical and operational challenges that hinder performance and flexibility. Rigid, hard-wired connections restrict head configurations, while probe transfers between chambers risk compromising vacuum integrity. Large instrument footprints and cumbersome navigation systems make operation in confined ultra-high vacuum (UHV) and high magnetic field environments particularly difficult. Cryogen-free STM setups are further hampered by pulse tube-induced vibrations that degrade imaging quality, and conventional large vertical translation stages add maintenance burden, higher operating costs, and extended pump-down times. The lack of multi-modal capability within a single instrument limits experimental versatility, while vacuum leaks and dead space introduced during probe translation create additional inefficiencies that slow research progress.</p>

<p ></p>

<p >Rutgers inventors have developed a novel modular SPM head featuring a unique weak spring and pin electrical connection system that allows easy mechanical and electrical coupling. This design supports in situ switching among scanning tunneling microscopy (STM), atomic force microscopy (AFM), and magnetic force microscopy (MFM) modes and facilitates transfer between atmospheric pressure, UHV chambers, and cryogenic or high magnetic field environments without breaking vacuum. The compact probe transfer mechanism replaces bulky traditional translation stages with a small-footprint, flexible design that shuttles probes between spatially separated sites within UHV systems, significantly reducing system size, pump down times, and leakage risks while improving measurement precision under demanding experimental conditions.</p>

<p ><strong> Market Applications: </strong></p>

<ul>
	<li >Advanced materials &amp; nanotechnology labs requiring compact, modular, multi-modal SPM solutions.</li>
	<li >Low-temperature, high magnetic field &amp; cryogen-free research facilities demanding atomic-resolution STM imaging.</li>
	<li >Quantum materials &amp; surface science research requiring precise, reliable probe exchange in controlled environments.</li>
	<li >Academic, industrial R&amp;D &amp; cryogenic instrumentation manufacturers seeking flexible, vibration-sensitive SPM upgrades.</li>
</ul>

<p ><strong>Advantages:</strong></p>

<ul>
	<li >Modular plug-and-play design enables flexible multi-modal integration across multiple UHV systems, supporting effortless switching between STM, AFM, and MFM without breaking vacuum.</li>
	<li >Compact all-in-one architecture integrates movement and vibration isolation into a reduced footprint, enabling atomic-resolution STM imaging in cryogen-free cryostats.</li>
	<li >Enhanced reliability and stability through automatic height locking, separate vacuum seals, and real-time sensors minimizing experimental disruptions.</li>
</ul>

<p ><strong>Publications: </strong></p>

<ul>
	<li >&bull; <a href="https://doi.org/10.1063/5.0212244"  target="_blank">Coe, Angela M., Guohong Li, and Eva Y. Andrei. &quot;Cryogen-free modular scanning tunneling microscope operating at 4-K in high magnetic field on a compact ultra-high vacuum platform.&quot;&nbsp;<em>Review of Scientific Instruments</em>&nbsp;95.8 (2024).</a> <a href="https://doi.org/10.1063/5.0212244"  target="_blank">https://doi.org/10.1063/5.0212244</a> </li>
	<li >&bull; Coe, Angela M., Guohong Li, and Eva Y. Andrei. &quot;Flexible internal transporter with gravity-assisted mechanism for vertical transfer of microscope head.&quot;&nbsp;<em>Review of Scientific Instruments</em>&nbsp;96.5 (2025). <a href="https://doi.org/10.1063/5.0264135"  target="_blank">https://doi.org/10.1063/5.0264135</a></li>
</ul>

<p ><strong>Intellectual Property &amp; Development Status:&nbsp;&nbsp;</strong>&nbsp;Issued U.S. patents: US12098026B2, US11474127B2, US12360136B2.&nbsp;Pending U.S. divisional application: US20250033878A1.&nbsp;&nbsp;Pending U.S. non-provisional application. Available for licensing and/or research collaboration.&nbsp;For any business development and other collaborative partnerships, contact:&nbsp; <a href="mailto:marketingbd@research.rutgers.edu"  target="_blank">marketingbd@research.rutgers.edu</a> </p>]]></description><pubDate>Fri, 10 Apr 2026 07:39:21 GMT</pubDate><author>christopher.perkins@rutgers.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Modular_Scanning_Probe_Microscopy_(SPM)_Head_and_Compact_UHV_Probe_Transfer_System</guid><dataField:caseId>MP-2025-010P</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 07:39:21 GMT</dataField:lastUpdateDate><dataField:Image><![CDATA[</span></span></span></span></p>

<p style="margin-bottom:11px; text-align:center"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">​</span></span></span></span></span><img src="https://rutgers.technologypublisher.com/files/sites/mp-2025-010p_image-20260410103603-1.png" style="height:15px; width:15px" /><img src="https://rutgers.technologypublisher.com/files/sites/image1946.png" style="display:block; margin-left:auto; margin-right:auto" /></p>

<p style="margin-bottom:11px; text-align:center"><span style="font-size:9.0pt"><span style="line-height:115%"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="color:#221e1f">Connection of STM head to transfer mechanism in RT chamber</span></span></span></span></p>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Image><dataField:AlgoliaSummary><![CDATA[</span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Traditional scanning probe microscopy (SPM) systems face a range of significant technical and operational challenges that hinder performance and flexibility. Rigid, hard-wired connections restrict head configurations, while probe transfers between chambers risk compromising vacuum integrity. Large instrument footprints and cumbersome navigation systems make operation in confined ultra-high vacuum (UHV) and high magnetic field environments particularly difficult. Cryogen-free STM setups are further hampered by pulse tube-induced vibrations that degrade imaging quality, and conventional large vertical translation stages add maintenance burden, higher operating costs, and extended pump-down times. The lack of multi-modal capability within a single instrument limits experimental versatility, while vacuum leaks and dead space introduced during probe translation create additional inefficiencies that slow research progress.</span></span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:AlgoliaSummary><dataField:Left><![CDATA[<strong>Invention Summary:</strong> </span></span></span></span></p>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"></span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Traditional scanning probe microscopy (SPM) systems face a range of significant technical and operational challenges that hinder performance and flexibility. Rigid, hard-wired connections restrict head configurations, while probe transfers between chambers risk compromising vacuum integrity. Large instrument footprints and cumbersome navigation systems make operation in confined ultra-high vacuum (UHV) and high magnetic field environments particularly difficult. Cryogen-free STM setups are further hampered by pulse tube-induced vibrations that degrade imaging quality, and conventional large vertical translation stages add maintenance burden, higher operating costs, and extended pump-down times. The lack of multi-modal capability within a single instrument limits experimental versatility, while vacuum leaks and dead space introduced during probe translation create additional inefficiencies that slow research progress.</span></span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif"></span></span></span></span></span></p>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Rutgers inventors have developed a novel modular SPM head featuring a unique weak spring and pin electrical connection system that allows easy mechanical and electrical coupling. This design supports in situ switching among scanning tunneling microscopy (STM), atomic force microscopy (AFM), and magnetic force microscopy (MFM) modes and facilitates transfer between atmospheric pressure, UHV chambers, and cryogenic or high magnetic field environments without breaking vacuum. The compact probe transfer mechanism replaces bulky traditional translation stages with a small-footprint, flexible design that shuttles probes between spatially separated sites within UHV systems, significantly reducing system size, pump down times, and leakage risks while improving measurement precision under demanding experimental conditions.</span></span></span></span></span></span><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Left><dataField:Right><![CDATA[<strong> Market Applications: </strong></span></span></span></span></p>

<ul>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="tab-stops:list 0in left 145.5pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Advanced materials &amp; nanotechnology labs requiring compact, modular, multi-modal SPM solutions.</span></span></span></span></span></span></span></li>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="tab-stops:list 0in left 145.5pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Low-temperature, high magnetic field &amp; cryogen-free research facilities demanding atomic-resolution STM imaging.</span></span></span></span></span></span></span></li>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="tab-stops:list 0in left 145.5pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Quantum materials &amp; surface science research requiring precise, reliable probe exchange in controlled environments.</span></span></span></span></span></span></span></li>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="tab-stops:list 0in left 145.5pt"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Academic, industrial R&amp;D &amp; cryogenic instrumentation manufacturers seeking flexible, vibration-sensitive SPM upgrades.</span></span></span></span></span></span></span></li>
</ul>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-family:&quot;Palatino Linotype&quot;,serif">Advantages:</span></strong></span></span></span></p>

<ul>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Modular plug-and-play design enables flexible multi-modal integration across multiple UHV systems, supporting effortless switching between STM, AFM, and MFM without breaking vacuum.</span></span></span></span></span></span></li>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Compact all-in-one architecture integrates movement and vibration isolation into a reduced footprint, enabling atomic-resolution STM imaging in cryogen-free cryostats.</span></span></span></span></span></span></li>
	<li style="text-align:justify"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Enhanced reliability and stability through automatic height locking, separate vacuum seals, and real-time sensors minimizing experimental disruptions.</span></span></span></span></span></span></li>
</ul>

<p style="margin-bottom:11px"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-family:&quot;Palatino Linotype&quot;,serif">Publications: </span></strong></span></span></span></p>

<ul>
	<li style="margin-left: -42px; text-align: justify;"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">&bull; </span></span><a href="https://doi.org/10.1063/5.0212244" style="color:blue; text-decoration:underline" target="_blank"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Coe, Angela M., Guohong Li, and Eva Y. Andrei. &quot;Cryogen-free modular scanning tunneling microscope operating at 4-K in high magnetic field on a compact ultra-high vacuum platform.&quot;&nbsp;<em>Review of Scientific Instruments</em>&nbsp;95.8 (2024).</span></span></a> <a href="https://doi.org/10.1063/5.0212244" style="color:blue; text-decoration:underline" target="_blank"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">https://doi.org/10.1063/5.0212244</span></span></a> </span></span></span></span></li>
	<li style="margin-left: -42px; text-align: justify;"><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">&bull; </span></span><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Coe, Angela M., Guohong Li, and Eva Y. Andrei. &quot;Flexible internal transporter with gravity-assisted mechanism for vertical transfer of microscope head.&quot;&nbsp;<em>Review of Scientific Instruments</em>&nbsp;96.5 (2025).</span></span> <a href="https://doi.org/10.1063/5.0264135" style="color:blue; text-decoration:underline" target="_blank"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">https://doi.org/10.1063/5.0264135</span></span></a></span></span></span></span></li>
</ul>

<p style="margin-bottom:11px; text-align:justify"><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><strong><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">Intellectual Property &amp; Development Status:&nbsp;&nbsp;</span></span></strong></span></span></span><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">&nbsp;Issued U.S. patents: US12098026B2, US11474127B2, US12360136B2.&nbsp;</span></span></span></span></span></span><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">Pending U.S. divisional application: US20250033878A1.&nbsp;</span></span></span></span></span></span><span style="font-size:11pt"><span style="text-justify:inter-ideograph"><span style="line-height:normal"><span style="font-family:Calibri,sans-serif"><span style="font-size:10.0pt"><span style="font-family:&quot;Times New Roman&quot;,serif">&nbsp;Pending U.S. non-provisional application</span></span></span></span></span></span><span style="font-size:12pt"><span style="line-height:normal"><span style="font-family:&quot;Times New Roman&quot;,serif"><span style="font-size:11.0pt"><span style="background-color:white"><span style="font-family:&quot;Palatino Linotype&quot;,serif"><span style="color:#242424">. Available for licensing and/or research collaboration.&nbsp;For any business development and other collaborative partnerships, contact:&nbsp; </span></span></span></span><a href="mailto:marketingbd@research.rutgers.edu" style="color:#0563c1; text-decoration:underline" target="_blank"><span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">marketingbd@research.rutgers.edu</span></span></a> <span style="font-size:11.0pt"><span style="font-family:&quot;Palatino Linotype&quot;,serif">]]></dataField:Right><dataField:inventorList></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Eusebio</dataField:firstName><dataField:lastName>Pires</dataField:lastName><dataField:title>TechAdvance Manager</dataField:title><dataField:department>Research Commercialization</dataField:department><dataField:emailAddress>ep620@research.rutgers.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Physical Sciences & Engineering]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Nucleophosmin 1 (NPM1) Mutation-Specific T Cell Receptors for Targeted Treatment of Acute Myeloid Leukemia</title><link>https://canberra-ip.technologypublisher.com/tech/Nucleophosmin_1_(NPM1)_Mutation-Specific_T_Cell_Receptors_for_Targeted_Treatment_of_Acute_Myeloid_Leukemia</link><description><![CDATA[<h2>Summary:&nbsp;</h2>

<p>The NCI seeks research co-development partners or licensees for Nucleophosmin 1 (NPM1) Mutation-Specific T Cell Receptors for Targeted Treatment of Acute Myeloid Leukemia.</p>

<h2>Description of Technology:&nbsp;</h2>

<p>Acute myeloid leukemia (AML) is a rare form of blood cancer affecting myeloid stem and progenitor cells, associated with a poor prognosis and a 5-year survival rate of ~33%. Current treatments, including intensive chemotherapy and stem cell transplantation, are not suitable for all patients and can cause significant toxicities, including low blood cell counts, infection and graft-versus-host disease. Therefore, there is a need for safer and more effective treatments.&nbsp;</p>

<p>This specific invention concerns the isolation of two highly specific T cell receptors (TCRs), known as TCR6 and TCR7, recognizing a neoepitope, AVEEVSLRK. The neoepitope is derived from mutant Nucleophosmin 1 (NPM1) and presented in the context of HLA-A*11:01. Pre-clinical results for these TCRs revealed robust and specific cytotoxicity against a leukemia cell line and several patient-derived AML samples expressing the NPM1 mutation and HLA-A*11:01. Furthermore, they showed no cross-reactivity to normal peripheral blood mononuclear cells, structurally similar peptides or unrelated HLA alleles. These results suggest these novel TCRs represent a potential adoptive T cell therapy for the treatment of AML.</p>

<h2>Potential Commercial Applications:&nbsp;</h2>

<ul>
	<li>Acute myeloid leukemia patients expressing HLA-A*11:01.&nbsp;</li>
</ul>

<h2>Competitive Advantages:</h2>

<ul>
	<li>Highly specific targeting of mutant NPM1</li>
	<li>Minimed off-target effects with enhanced safety profile</li>
	<li>&bull;Significant unmet medical need for AML patients</li>
</ul>]]></description><pubDate>Fri, 10 Apr 2026 06:41:17 GMT</pubDate><author>nihott@nih.gov</author><guid>https://canberra-ip.technologypublisher.com/tech/Nucleophosmin_1_(NPM1)_Mutation-Specific_T_Cell_Receptors_for_Targeted_Treatment_of_Acute_Myeloid_Leukemia</guid><dataField:caseId>TAB-5097</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 06:45:33 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Vid</dataField:firstName><dataField:lastName>Leko</dataField:lastName><dataField:title>Physician Scientist Early Investigator</dataField:title><dataField:department>Immune Deficiency Cellular Therapy Program</dataField:department><dataField:emailAddress>vid.leko@nih.gov</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Aidan</dataField:firstName><dataField:lastName>Pursley</dataField:lastName><dataField:title>Fellow</dataField:title><dataField:department></dataField:department><dataField:emailAddress>aidan.pursley@nih.gov</dataField:emailAddress><dataField:phoneNumber>240-858-7867</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Kenichi</dataField:firstName><dataField:lastName>Hanada</dataField:lastName><dataField:title>Staff Scientist/Visiting Scientist</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>HanadaK@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>240-858-3774</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Zhiya</dataField:firstName><dataField:lastName>Yu</dataField:lastName><dataField:title>Research Fellow</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>zhiya_yu@nih.gov</dataField:emailAddress><dataField:phoneNumber>240-858-3812</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Catherine</dataField:firstName><dataField:lastName>Ade</dataField:lastName><dataField:title>CRTA Post-Doctoral Fellow</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>Catherine.ade@nih.gov</dataField:emailAddress><dataField:phoneNumber>240-760-6154</dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>James</dataField:firstName><dataField:lastName>Yang</dataField:lastName><dataField:title>Senior Principal Investigator</dataField:title><dataField:department>CCR</dataField:department><dataField:emailAddress>JamesYang@mail.nih.gov</dataField:emailAddress><dataField:phoneNumber>301-496-1574</dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Abritee</dataField:firstName><dataField:lastName>Dhal</dataField:lastName><dataField:title>Technology Transfer Manager</dataField:title><dataField:department></dataField:department><dataField:emailAddress>abritee.dhal@nih.gov</dataField:emailAddress><dataField:phoneNumber>301-451-2796</dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Application > Therapeutics| TherapeuticArea > Oncology| Collaboration Sought > Collaboration| Collaboration Sought > Licensing]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Vegetation Anchoring System for Coastal Restoration</title><link>https://canberra-ip.technologypublisher.com/tech/Vegetation_Anchoring_System_for_Coastal_Restoration</link><description><![CDATA[<h3><em>Secures Landscape Plant Plugs, Preventing Displacement Due to Environmental Forces</em></h3>

<p>This vegetation anchoring device secures plants used for coastal restoration projects. Coastal wetlands and shorelines provide important ecological services, including storm protection, improved water quality, and habitat for wildlife. However, erosion, storm activity, and rising sea levels are degrading many of these environments, increasing the need for effective coastal restoration strategies. The global coastal protection systems market size reached $18 billion USD in 2024 and is expected to reach $46 billion USD by 2033, with a compound aggregate growth rate of 12.60%. Coastal restoration projects often involve planting vegetation using landscape plugs, which are small, containerized plants with established roots that are easy to transport and plant in large quantities. Existing erosion control methods can help stabilize shorelines, but they are not designed to hold individual plant plugs. Additionally, currents and sediment movement can dislodge newly planted vegetation in coastal environments before roots have fully developed. There is a need for anchoring devices specifically designed to withstand harsh coastal environmental conditions.</p>

<p>&nbsp;</p>

<p>Researchers at the University of Florida are developing a carrier for plants to help secure and anchor vegetation used in coastal restoration. The device is designed specifically to hold landscape plant plugs in place in coastal substrates where traditional stakes or containers are ineffective due to soft sediments and harsh environmental conditions.</p>

<p>&nbsp;</p>

<h3>Application</h3>

<p>Anchors plant plugs in place, reducing the risk of displacing newly planted vegetation used in coastal restoration and shoreline stabilization projects</p>

<p>&nbsp;</p>

<h3>Advantages</h3>

<ul>
	<li>Keeps newly planted vegetation in place, enabling root systems to establish themselves in the surrounding substrate</li>
	<li>Includes openings for water circulation, supporting root growth into the surrounding sediment</li>
	<li>Designed for installation without specialized equipment, enabling manual deployment in restoration sites</li>
	<li>Manufactured using biodegradable material, ensuring the anchors do not persist in the aquatic environment</li>
</ul>

<p>&nbsp;</p>

<h3>Technology</h3>

<p>The system uses three primary components&mdash;a perforated basket, a thread cap, and an insertion spike&mdash;function together to secure a landscape plant plug in coastal substrates. The perforated basket holds the plant plug and its growing medium while allowing water movement and root growth through the surrounding openings. The threaded cap then attaches to the basket and secures the plug in position, enabling it to remain stable during environmental exposure. Finally, extending from the bottom of the basket is an insertion spike that penetrates the coastal substrate and anchors the device in place. The anchor is required only during the time the plant establishes a root system; therefore, the anchors are produced using biodegradable materials to ensure they do not persist in the aquatic environment. The device gradually breaks down after the vegetation becomes established.</p>]]></description><pubDate>Fri, 10 Apr 2026 05:52:35 GMT</pubDate><author>saradagen@ufl.edu</author><guid>https://canberra-ip.technologypublisher.com/tech/Vegetation_Anchoring_System_for_Coastal_Restoration</guid><dataField:caseId>MP26032</dataField:caseId><dataField:lastUpdateDate>Fri, 10 Apr 2026 06:12:04 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Julie</dataField:firstName><dataField:lastName>Bruck</dataField:lastName><dataField:title>Faculty</dataField:title><dataField:department>DCP-LANDSCAPE ARCHITECTURE</dataField:department><dataField:emailAddress>jbruck@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Christopher</dataField:firstName><dataField:lastName>Bonura</dataField:lastName><dataField:title>Employee</dataField:title><dataField:department>DCP-LANDSCAPE ARCHITECTURE</dataField:department><dataField:emailAddress>c.bonura@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Lenny</dataField:firstName><dataField:lastName>Terry</dataField:lastName><dataField:title>Assistant Director</dataField:title><dataField:department>OR-TECHNOLOGY LICENSING</dataField:department><dataField:emailAddress>lterry@ufl.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Technology Classifications > Engineering > Civil| Technology Classifications > Engineering > Materials]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>AI-Driven Security Framework for Over-the-Air Computation in Concentrated Solar Power Systems</title><link>https://canberra-ip.technologypublisher.com/tech/AI-Driven_Security_Framework_for_Over-the-Air_Computation_in_Concentrated_Solar_Power_Systems</link><description><![CDATA[<div ><strong>Invention Description</strong></div>

<div >Concentrated Solar Power (CSP) systems increasingly rely on real-time data aggregation through advanced communication frameworks such as Over-the-Air Computation (AirComp) in emerging 6G-IoT environments. However, these systems are vulnerable to signal interference and jamming attacks, which can disrupt data transmission and compromise system performance. Both simple and coordinated attacks pose significant risks to the reliability and efficiency of energy operation.</div>

<div >&nbsp;</div>

<div >Researchers at Arizona State University have developed a robust security framework designed to protect AirComp-enabled CSP systems from jamming attacks. The technology leverages AI-driven statistical signal analysis, adaptive detection thresholds and spatially-aware mitigation strategies to identify and counteract interference. It can effectively detect and neutralize both basic and coordinated jamming attempts, ensuring reliable and continuous data aggregation. This approach enhances system resilience and supports optimal performance in next-generation 6G-IoT energy networks.</div>

<div >&nbsp;</div>

<div >This AI-powered security framework ensures reliable data aggregation and resilience against jamming attacks in AirComp-enabled Concentrated Solar Power systems.</div>

<div >&nbsp;</div>

<div ><strong>Potential Applications</strong></div>

<ul>
	<li >Enhancing security and performance of Concentrated Solar Power plants with real-time IoT data aggregation</li>
	<li >Deployment in 6G-enabled Industrial IoT networks requiring robust, low-latency communication</li>
	<li >Integration into smart grid energy management systems</li>
	<li >Use in critical infrastructure monitoring where resilience against signal interference is mandatory</li>
</ul>

<div ><strong>Benefits and Advantages</strong></div>

<ul>
	<li >AI-based differentiation between legitimate sensor data and malicious interference using binary hypothesis testing</li>
	<li >Dynamic threshold adjustment through reinforcement learning for optimized attack detection sensitivity</li>
	<li >Secure enrollment phase for reliable node registration and baseline profiling</li>
	<li >Power allocation strategy minimizing errors under power constraints</li>
	<li >Hierarchical defense combining signal fingerprinting, adaptive beamforming, and node ejection protocols</li>
	<li >Experimental validation proving significant improvements in data aggregation and attack detection</li>
</ul>

<div >For more information about this opportunity, please see</div>

<div ><a href="https://ieeexplore.ieee.org/document/11151639" target="_blank">Adhikary et al - IEEE IoT-J - 2025</a></div>]]></description><pubDate>Thu, 09 Apr 2026 16:00:18 GMT</pubDate><author>ip@skysonginnovations.com</author><guid>https://canberra-ip.technologypublisher.com/tech/AI-Driven_Security_Framework_for_Over-the-Air_Computation_in_Concentrated_Solar_Power_Systems</guid><dataField:caseId>M25-329P</dataField:caseId><dataField:lastUpdateDate>Thu, 09 Apr 2026 16:00:18 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Eirini Eleni</dataField:firstName><dataField:lastName>Tsiropoulou</dataField:lastName><dataField:title>Associate Professor</dataField:title><dataField:department>Electrical, Computer and Energy Engineering</dataField:department><dataField:emailAddress>eirini@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Dipanjan</dataField:firstName><dataField:lastName>Adhikary</dataField:lastName><dataField:title>Mr.</dataField:title><dataField:department>School of Electrical, Computer and Energy Engineering</dataField:department><dataField:emailAddress>dadhika6@asu.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Physical Sciences</dataField:firstName><dataField:lastName>Team</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress></dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Artificial Intelligence/Machine Learning| Energy & Power| Environmental| Physical Science| Intelligence & Security]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item><item><title>Method for formation, compaction, sealing and disposal of CO2 hydrates on the seabed</title><link>https://canberra-ip.technologypublisher.com/tech?title=Method_for_formation%2c_compaction%2c_sealing_and_disposal_of_CO2_hydrates_on_the_seabed</link><description><![CDATA[<h2>Background:&nbsp;</h2>

<p>The rising levels of atmospheric carbon dioxide (CO2) present a critical global challenge, significantly contributing to climate change and ocean acidification. Current CO2&nbsp;sequestration methods, such as geological storage, face&nbsp;numerous&nbsp;hurdles, including leakage risks,&nbsp;high costs, and the need for extensive monitoring. An emerging method involves the formation, compaction, sealing, and disposal of CO2&nbsp;hydrates on the seabed. CO2&nbsp;hydrates are solid, ice-like structures that form under high-pressure, low-temperature conditions unique to the ocean floor. This method offers several advantages over traditional storage techniques, including increased stability, reduced risk of leakage, and the potential for long-term, large-scale CO2&nbsp;storage. However, the artificial synthesis of CO2&nbsp;hydrates&nbsp;is slow,&nbsp;hindered&nbsp;the development of hydrate-based industrial technologies. The fastest reported CO2&nbsp;hydrate formation rate is 20&nbsp;g/L/hr, insufficient for large-scale carbon sequestration.&nbsp;Therefore&nbsp;it is crucial to&nbsp;promote faster hydrate growth&nbsp;in order to&nbsp;achieve&nbsp;gigascale&nbsp;CO2&nbsp;sequestration through hydrate formation.</p>

<p>&nbsp;</p>

<h2>Technology Overview:&nbsp;</h2>

<p>This technology provides a comprehensive solution for the formation, compaction, sealing, and disposal of CO2&nbsp;hydrates on the seabed, addressing the major challenge of slow hydrate formation. The process begins with the rapid formation of CO2&nbsp;hydrates in a bubble column reactor, where CO2&nbsp;is recirculated to enhance the formation rate. This approach significantly accelerates hydrate formation&nbsp;(800 g/L/hr), overcoming the limitations of traditional methods. Once formed, the CO2&nbsp;hydrates are compacted into dense plugs, ensuring stability and ease of handling. These plugs are then sealed to prevent dissociation and leakage during transport. The sealed CO2&nbsp;hydrate plugs are transported to the seabed,&nbsp;leveraging&nbsp;natural oceanic conditions to&nbsp;maintain&nbsp;their stability. Finally, the plugs are disposed of on the seabed, where the high-pressure, low-temperature environment ensures their long-term stability and prevents CO2&nbsp;from escaping back into the atmosphere. This method offers a scalable and efficient approach to CO2&nbsp;sequestration, providing&nbsp;a viable&nbsp;solution for reducing atmospheric CO2&nbsp;levels and mitigating the impacts of climate change.&nbsp;</p>

<p>&nbsp;</p>

<p><img src="https://utotc.technologypublisher.com/files/sites/7995_bah_image-20260409155408-1.png"  /></p>

<h2>Benefits&nbsp;</h2>

<ul>
	<li>
	<p>This method&nbsp;utilizes&nbsp;a bubble column reactor with CO2&nbsp;recirculation to significantly speed up CO2&nbsp;hydrate formation&nbsp;to rates of 800 g/L/hr, overcoming the slow rates that hinder traditional methods.&nbsp;&nbsp;</p>
	</li>
</ul>

<ul>
	<li>
	<p>The method is designed for large-scale application, making it&nbsp;feasible&nbsp;to achieve gigaton-scale carbon sequestration.&nbsp;</p>
	</li>
</ul>

<ul>
	<li>
	<p>The sealing process prevents CO2&nbsp;hydrate plugs from breaking down during transport, ensuring safe delivery to the seabed.&nbsp;</p>
	</li>
</ul>

<p>&nbsp;</p>

<h2>Applications&nbsp;&nbsp;</h2>

<ul>
	<li>
	<p>Oil and gas&nbsp;</p>
	</li>
</ul>

<ul>
	<li>
	<p>Carbon sequestration&nbsp;</p>
	</li>
</ul>

<ul>
	<li>
	<p>Chemical manufacturing&nbsp;</p>
	</li>
</ul>

<p>&nbsp;</p>

<h2>Opportunity&nbsp;</h2>

<ul>
	<li>
	<p>This novel&nbsp;method for CO2 hydrate formation is scalable and the fastest reported rate in the industry, making&nbsp;it&nbsp;feasible&nbsp;to achieve gigaton-scale carbon sequestration.&nbsp;</p>
	</li>
</ul>

<ul>
	<li>
	<p>Available for licensing</p>
	</li>
</ul>]]></description><pubDate>Thu, 09 Apr 2026 13:56:39 GMT</pubDate><author>intranet@discoveries.utexas.edu</author><guid>https://canberra-ip.technologypublisher.com/tech?title=Method_for_formation%2c_compaction%2c_sealing_and_disposal_of_CO2_hydrates_on_the_seabed</guid><dataField:caseId>7995 BAH</dataField:caseId><dataField:lastUpdateDate>Thu, 09 Apr 2026 13:56:39 GMT</dataField:lastUpdateDate><dataField:inventorList><dataField:inventor><dataField:firstName>Vaibhav</dataField:firstName><dataField:lastName>Bahadur</dataField:lastName><dataField:title></dataField:title><dataField:department>Mech Eng</dataField:department><dataField:emailAddress>vb@austin.utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Awan</dataField:firstName><dataField:lastName>Bhati</dataField:lastName><dataField:title>Graduate Research Assistant</dataField:title><dataField:department>Mechanical Engineering</dataField:department><dataField:emailAddress>bhati137@utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>ManojKumar</dataField:firstName><dataField:lastName>Lokanathan</dataField:lastName><dataField:title>Graduate Research Assistant</dataField:title><dataField:department>Mechanical Engineering</dataField:department><dataField:emailAddress>manoj.l@utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor><dataField:inventor><dataField:firstName>Steve</dataField:firstName><dataField:lastName>Smaha</dataField:lastName><dataField:title></dataField:title><dataField:department></dataField:department><dataField:emailAddress>stevesmaha@gmail.com</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:inventor></dataField:inventorList><dataField:keywords></dataField:keywords><dataField:licensingContactList><dataField:licensingContact><dataField:firstName>Ashwin</dataField:firstName><dataField:lastName>Ramanujam</dataField:lastName><dataField:title>Business Development Specialist</dataField:title><dataField:department>Discovery to Impact</dataField:department><dataField:emailAddress>ashwin.ramanujam@austin.utexas.edu</dataField:emailAddress><dataField:phoneNumber></dataField:phoneNumber></dataField:licensingContact></dataField:licensingContactList><dataField:categoryName><![CDATA[Physical sciences > Energy > Renewable, green, or transitional energy| Physical sciences > Environmental & sustainable solutions]]></dataField:categoryName><dataField:Patents></dataField:Patents><dataField:customParameters></dataField:customParameters><dataField:isFeatured>False</dataField:isFeatured></item></channel></rss>