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Porous silicon–graphene oxide core–shell nanoparticles for targeted delivery of siRNA to the injured brain

Author(s)
Joo, Jinmyoung; Kwon, Ester J; Kang, Jinyoung; Skalak, Matthew; Anglin, Emily J; Mann, Aman P; Ruoslahti, Erkki; Bhatia, Sangeeta N; Sailor, Michael J; ... Show more Show less
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Creative Commons Attribution-Noncommercial-Share Alike http://creativecommons.org/licenses/by-nc-sa/4.0/
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Abstract
© 2016 The Royal Society of Chemistry. We report the synthesis, characterization, and assessment of a nanoparticle-based RNAi delivery platform that protects siRNA payloads against nuclease-induced degradation and efficiently delivers them to target cells. The nanocarrier is based on biodegradable mesoporous silicon nanoparticles (pSiNPs), where the voids of the nanoparticles are loaded with siRNA and the nanoparticles are encapsulated with graphene oxide nanosheets (GO-pSiNPs). The graphene oxide encapsulant delays release of the oligonucleotide payloads in vitro by a factor of 3. When conjugated to a targeting peptide derived from the rabies virus glycoprotein (RVG), the nanoparticles show 2-fold greater cellular uptake and gene silencing. Intravenous administration of the nanoparticles into brain-injured mice results in substantial accumulation specifically at the site of injury.
Date issued
2016
URI
https://hdl.handle.net/1721.1/135749
Department
Harvard University--MIT Division of Health Sciences and Technology; Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science; Koch Institute for Integrative Cancer Research at MIT
Journal
Nanoscale Horiz.
Publisher
Royal Society of Chemistry (RSC)

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