4.7 Article

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

期刊

NANOSCALE HORIZONS
卷 1, 期 5, 页码 407-414

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6nh00082g

关键词

-

资金

  1. Defense Advanced Research Projects Agency (DARPA) [HR0011-13-2-0017]
  2. Marie-D. & Pierre Casimir-Lambert Fund (MIT)
  3. Sanford-Burnham-Prebys Medical Discovery Institute
  4. Ruth L. Kirschstein National Research Service Award [1F32CA177094-01]

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据