Efficient Functional Delivery of siRNA using Mesoporous Silica Nanoparticles with Ultralarge Pores

Authors
Na, Hee-KyungKim, Mi-HeePark, KihyunRyoo, Soo-RyoonLee, Kyung EunJeon, HyesungRyoo, RyongHyeon, ChangbongMin, Dal-Hee
Issue Date
2012-06-11
Publisher
WILEY-V C H VERLAG GMBH
Citation
SMALL, v.8, no.11, pp.1752 - 1761
Abstract
Among various nanoparticles, mesoporous silica nanoparticles (MSNs) have attracted extensive attention for developing efficient drug-delivery systems, mostly due to their high porosity and biocompatibility. However, due to the small pore size, generally below 5 nm in diameter, potential drugs that are loaded into the pore have been limited to small molecules. Herein, a small interfering RNA (siRNA) delivery strategy based on MSNs possessing pores with an average diameter of 23 nm is presented. The siRNA is regarded as a powerful gene therapeutic agent for treatment of a wide range of diseases by enabling post-transcriptional gene silencing, so-called RNA interference. Highly efficient, sequence-specific, and technically very simple target gene knockdown is demonstrated using MSNs with ultralarge pores of size 23 nm in vitro and in vivo without notable cytotoxicity.
Keywords
SMALL INTERFERING RNA; ENDOTHELIAL GROWTH-FACTOR; GENE; CELLS; THERAPEUTICS; CANCER; RESISTANT; PLANTS; SMALL INTERFERING RNA; ENDOTHELIAL GROWTH-FACTOR; GENE; CELLS; THERAPEUTICS; CANCER; RESISTANT; PLANTS; cancer therapy; drug delivery; mesoporous materials; nanoparticles; RNA interference
ISSN
1613-6810
URI
https://pubs.kist.re.kr/handle/201004/129149
DOI
10.1002/smll.201200028
Appears in Collections:
KIST Article > 2012
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE