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基于壳聚糖的 siRNA 递送系统。

Chitosan-based siRNA delivery systems.

机构信息

Pharmaceutics and Drug Delivery Group, Louvain Drug Research Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.

Pharmaceutics and Drug Delivery Group, Louvain Drug Research Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.

出版信息

J Control Release. 2013 Nov 28;172(1):207-218. doi: 10.1016/j.jconrel.2013.08.005. Epub 2013 Aug 18.

Abstract

Recently, chitosan has attracted significant attention in the formulation of small interfering RNA (siRNA). Because of its cationic nature, chitosan can easily complex siRNA, thus readily forming nanoparticles. Moreover, chitosan is biocompatible and biodegradable, which make it a good candidate for siRNA delivery in vivo. However, chitosan requires further development to achieve high efficiency. This review will describe the major barriers that impair the efficiency of the chitosan-based siRNA delivery systems, including the stability of the delivery system in biological fluids and endosomal escape. Several solutions to counteract these barriers have been developed and will be discussed. The parameters to consider for designing powerful delivery systems will be described, particularly the possibilities for grafting targeting ligands. Finally, optimized systems that allow in vivo therapeutic applications for both local and systemic delivery will be reviewed. This review will present recent improvements in chitosan-based siRNA delivery systems that overcome many of these system's previous pitfalls and pave the way to a new generation of siRNA delivery systems.

摘要

最近,壳聚糖在小干扰 RNA(siRNA)的制剂中引起了极大的关注。由于其带正电荷的性质,壳聚糖可以很容易地与 siRNA 复合,从而容易形成纳米颗粒。此外,壳聚糖具有生物相容性和可生物降解性,使其成为体内 siRNA 递送的良好候选物。然而,壳聚糖需要进一步开发才能实现高效率。这篇综述将描述影响壳聚糖基 siRNA 递送系统效率的主要障碍,包括递送系统在生物流体中的稳定性和内涵体逃逸。已经开发了几种克服这些障碍的解决方案,并将进行讨论。将描述用于设计强大递送系统的参数,特别是靶向配体嫁接的可能性。最后,将综述允许用于局部和全身递送的体内治疗应用的优化系统。这篇综述将介绍最近在壳聚糖基 siRNA 递送系统方面的改进,这些改进克服了这些系统以前的许多缺陷,为新一代 siRNA 递送系统铺平了道路。

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