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使用基于聚阳离子的纳米颗粒递送RNA干扰疗法。

Delivery of RNA interference therapeutics using polycation-based nanoparticles.

作者信息

Howard Kenneth Alan

机构信息

Interdisciplinary Nanoscience Center (iNANO), Department of Molecular Biology, University of Aarhus, 8000 Aarhus C, Denmark.

出版信息

Adv Drug Deliv Rev. 2009 Jul 25;61(9):710-20. doi: 10.1016/j.addr.2009.04.001. Epub 2009 Apr 5.

Abstract

RNAi-based therapies are dependent on extracellular and intracellular delivery of RNA molecules for enabling target interaction. Polycation-based nanoparticles (or polyplexes) formed by self-assembly with RNA can be used to modulate pharmacokinetics and intracellular trafficking to improve the therapeutic efficacy of RNAi-based therapeutics. This review describes the application of polyplexes for extracellular and intracellular delivery of synthetic RNA molecules. Focus is given to routes of administration and silencing effects in animal disease models. The inclusion of functional components into the nanoparticle for controlling cellular trafficking and RNA release is discussed. This work highlights the versatile nature of polycation-based nanoparticles to fulfil the delivery requirements for RNA molecules with flexibility in design to evolve alongside an expanding repertoire of RNAi-based drugs.

摘要

基于RNA干扰的疗法依赖于RNA分子的细胞外和细胞内递送以实现与靶点的相互作用。通过与RNA自组装形成的基于聚阳离子的纳米颗粒(或多聚体)可用于调节药代动力学和细胞内运输,以提高基于RNA干扰疗法的治疗效果。本综述描述了多聚体在合成RNA分子的细胞外和细胞内递送中的应用。重点关注动物疾病模型中的给药途径和沉默效果。讨论了将功能成分纳入纳米颗粒以控制细胞运输和RNA释放的问题。这项工作突出了基于聚阳离子的纳米颗粒的多功能性质,能够灵活满足RNA分子的递送要求,以随着基于RNA干扰药物种类的不断增加而发展。

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