A scaffold bearing eight terminal alkyne groups was synthesized from sucrose, and copies of an azide-terminated Gd-DOTA complex were attached via copper(I)-catalyzed azide-alkyne cycloaddition in this invention. This contrast agent (CA) was administered by gavage to C3H mice. Passage of the CA through the gastrointestinal (GI) tract was followed by T1-weighted magnetic resonance imaging (MRI) over a period of 48 hours. Thus, a new, orally administered, GI-specific CA for MRI has been developed and successfully demonstrated. Background: Gastrointestinal (GI) radiography using barium contrast media has been widely used as a first-choice diagnostic imaging modality for detection of GI pathologies. Colonoscopy is the standard of care for colorectal cancer (CRC) screening. However, colonoscopy is an invasive procedure that requires intravenous sedation and suffers from patient noncompliance. CT colonography (CT-C) has high sensitivity to identify large polyps, but sensitivity decreases with polyp size and radiation dosage is a concern. MRI colonography (MR-C) uses non-ionizing radiation and provides CRC lesion detection with high specificity, yet modest sensitivity. MR-C has been indicated in cases of incomplete colonoscopy, due to obstruction, and is increasingly being applied as a non-invasive screening tool without the need for sedation.
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