壳聚糖
体内
RNA干扰
体外
转染
小干扰RNA
化学
细胞内
纳米颗粒
细胞生物学
纳米技术
生物物理学
材料科学
生物
生物化学
核糖核酸
生物技术
基因
作者
Morten Østergaard Andersen,Kenneth A. Howard,Jørgen Kjems
出处
期刊:Methods in molecular biology
日期:2009-01-01
卷期号:: 77-86
被引量:23
标识
DOI:10.1007/978-1-60327-295-7_6
摘要
Delivery is a key issue in development of clinically relevant RNAi therapeutics. Polymeric nanoparticles formed by self-assembly of polycations with siRNA can be used for extracellular delivery, cellular uptake and intracellular trafficking as a strategy to improve the therapeutic potential of siRNA. This chapter describes a chitosan-based nanoparticle system for in vitro and in vivo transfection of siRNA into cells. The method exploits the mucoadhesive and mucopermeable properties of this cationic polysaccharide to deliver siRNA across mucosal epithelium and provides a platform for targeting human diseases with RNAi therapeutics.
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