| Literature DB >> 27031484 |
Eric A Tanifum1,2, Ketan Ghaghada1,2, Craig Vollert3, Elizabeth Head4, Jason L Eriksen3, Ananth Annapragada1,2.
Abstract
Amyloid binding molecules with greater hydrophilicity than existing ligands were synthesized. The lead candidate ET6-21 bound amyloid fibrils, and amyloid deposits in dog brain and human brain tissue ex vivo. The ligand was used to prepare novel amyloid-targeted liposomal nanoparticles. The preparation was tested in the Tg2576 and TetO/APP mouse models of amyloid deposition. Gd chelates and Indocyanine green were included in the particles for visualization by MRI and near-infrared microscopy. Upon intravenous injection, the particles successfully traversed the blood-brain barrier in these mice, and bound to the plaques. Magnetic resonance imaging (T1-MRI) conducted 4 days after injection demonstrated elevated signal in the brains of mice with amyloid plaques present. No signal was observed in amyloid-negative mice, or in amyloid-positive mice injected with an untargeted version of the same agent. The MRI results were confirmed by immunohistochemical and fluorescent microscopic examination of mouse brain sections, showing colocalization of the fluorescent tags and amyloid deposits.Entities:
Keywords: Alzheimer’s disease; amyloid angiopathy; amyloid plaque; gadolinium; imaging; liposome; magnetic resonance imaging; molecular imaging; nanoparticle
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Year: 2016 PMID: 27031484 PMCID: PMC4931553 DOI: 10.3233/JAD-151124
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472