| Literature DB >> 30300748 |
Kristen M Ahlschwede1, Geoffry L Curran2, Jens T Rosenberg3, Samuel C Grant3, Gobinda Sarkar4, Robert B Jenkins4, Subramanian Ramakrishnan3, Joseph F Poduslo2, Karunya K Kandimalla5.
Abstract
Accumulation of amyloid beta (Aβ) peptides in the cerebral vasculature, referred to as cerebral amyloid angiopathy (CAA), is widely observed in Alzheimer's disease (AD) brain and was shown to accelerate cognitive decline. There is no effective method for detecting cerebrovascular amyloid (CVA) and treat CAA. The targeted nanoparticles developed in this study effectively migrated from the blood flow to the vascular endothelium as determined by using quartz crystal microbalance with dissipation monitoring (QCM-D) technology. We also improved the stability, and blood-brain barrier (BBB) transcytosis of targeted nanoparticles by coating them with a cationic BBB penetrating peptide (K16ApoE). The K16ApoE-Targeted nanoparticles demonstrated specific targeting of vasculotropic DutchAβ40 peptide accumulated in the cerebral vasculature. Moreover, K16ApoE-Targeted nanoparticles demonstrated significantly greater uptake into brain and provided specific MRI contrast to detect brain amyloid plaques.Entities:
Keywords: Alzheimer's disease (AD); BBB permeating peptide; Cerebrovascular amyloid; Magnetic resonance imaging (MRI); Targeted nanoparticles
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Year: 2018 PMID: 30300748 DOI: 10.1016/j.nano.2018.09.010
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307