| Literature DB >> 29732165 |
Jinmyoung Joo1, Ester J Kwon2, Jinyoung Kang3, Matthew Skalak2, Emily J Anglin1, Aman P Mann4, Erkki Ruoslahti4,5, Sangeeta N Bhatia2,6,7,8,9,10, Michael J Sailor1,3.
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 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.Entities:
Year: 2016 PMID: 29732165 PMCID: PMC5935492 DOI: 10.1039/C6NH00082G
Source DB: PubMed Journal: Nanoscale Horiz ISSN: 2055-6756 Impact factor: 10.989