The field of pharmaceutical manufacturing is rapidly evolving to meet increasing demands for personalized drug delivery, precise dosage forms, and consistent controlled-release profiles. As healthcare shifts toward individualized treatment plans, clinicians and researchers are seeking advanced manufacturing solutions that deliver compact, robust, and high drug-loading formulations. Additive manufacturing, particularly powder bed fusion methods, offers a promising route, but widespread adoption is limited by persistent processing and formulation challenges.
Traditional powder-based 3D printing approaches often struggle with poor powder flow, leading to uneven layer deposition and inconsistent product formation. High porosity and rapid disintegration further undermine the structural integrity and release control of printed dosage forms. Additionally, the need for pre-treatment or flow-enhancing additives can introduce variability in drug content and compromise long-term stability. These limitations hinder the creation of reliable, scalable systems for patient-specific medications and high-dose applications.
This technology introduces a hot-melt granulation process where a therapeutic compound is blended with a low melting point lipid. Upon heating and extrusion, the lipid uniformly coats drug particles, resulting in free-flowing granules ideal for selective laser melting (SLM)-based powder bed fusion. During SLM, the coated granules are fused into dense tablets with low porosity, high drug loading, and tunable extended-release profiles. Optional formulation enhancements—such as lower melting lipids or polymers—help reduce thermal degradation during laser fusion.
This method offers a solvent-free, scalable, and structurally robust alternative to traditional powder bed fusion systems. By integrating granulation and SLM, the technology improves powder flowability, enables consistent layer fusion, and minimizes burst release. It produces compact dosage forms with precise drug content and controlled release kinetics, making it especially suitable for personalized therapeutics and continuous pharmaceutical manufacturing.
Provisional patent 63/710,474 filed