A New Delivery System for Double Stranded siRNA Oligonucleotides Based on Gelatin Nanoparticles

J. Zillies, C. Coester
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引用次数: 2

Abstract

The selective suppression or elimination of the function of individual proteins, enabled by the mechanisms of RNA Interference, is a new promising approach in the treatment of various diseases. The minor in vitro transfection rates besides the poor in vivo stability wellknown for "naked" double stranded siRNA oligonucleotides raise the question of how to accomplish in vitro or even in vivo transfection. Due to their advantageous properties in drug delivery and drug targeting, nanoparticulate carrier systems lend themselves to an application in siRNA transfection. Thus, the aim of this study was to show that nanoparticles made of gelatin can be used as a potential drug delivery system for double stranded siRNA oligonucleotides.
一种新的基于明胶纳米颗粒的双链siRNA寡核苷酸递送系统
通过RNA干扰机制,选择性抑制或消除单个蛋白质的功能,是治疗各种疾病的一种有前途的新方法。除了众所周知的“裸”双链siRNA寡核苷酸体内稳定性差之外,体外转染率低,这就提出了如何完成体外甚至体内转染的问题。由于其在药物传递和药物靶向方面的优势,纳米颗粒载体系统可以应用于siRNA转染。因此,本研究的目的是表明由明胶制成的纳米颗粒可以用作双链siRNA寡核苷酸的潜在药物递送系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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