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

Nanoscale Horiz
Authors
Abstract

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 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.

Year of Publication
2016
Journal
Nanoscale Horiz
Volume
1
Issue
5
Pages
407-414
Date Published
2016 Sep 01
ISSN
2055-6764
DOI
10.1039/C6NH00082G
PubMed ID
29732165
PubMed Central ID
PMC5935492
Links
Grant list
Howard Hughes Medical Institute / United States
F32 CA177094 / CA / NCI NIH HHS / United States