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利用脂质纳米颗粒体内递送 RNAi。

In vivo delivery of RNAi with lipid-based nanoparticles.

机构信息

Division of Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, NC 27599-7571, USA.

出版信息

Annu Rev Biomed Eng. 2011 Aug 15;13:507-30. doi: 10.1146/annurev-bioeng-071910-124709.

Abstract

RNA interference (RNAi) technology represents a fundamentally new category of treatments for human disease by addressing targets that are traditionally considered undruggable with existing medicines. The major challenge for RNAi-based therapy is the delivery system that meets human therapeutic needs. Therefore, engineering vectors with good delivery efficiency and safety profile is an intense area of research. Lipid-based nanoparticles for RNAi have yielded successful advances in vivo and to an extent in clinical trials. In this review, we discuss the barriers in developing lipid-based nanoparticles for in vivo RNAi and different strategies to overcome them. Rational designs that address safety concerns and ensure effective delivery will aid the translation of engineered lipid-based nanoparticles toward the clinic in the foreseeable future.

摘要

RNA 干扰 (RNAi) 技术通过针对传统上认为现有药物无法治疗的靶点,为人类疾病的治疗提供了一种全新的治疗方法。基于 RNAi 的治疗的主要挑战是满足人类治疗需求的输送系统。因此,具有良好输送效率和安全特性的工程载体是一个研究热点。用于 RNAi 的基于脂质的纳米颗粒在体内和一定程度的临床试验中取得了成功进展。在这篇综述中,我们讨论了为体内 RNAi 开发基于脂质的纳米颗粒所面临的障碍,以及克服这些障碍的不同策略。解决安全问题并确保有效传递的合理设计将有助于在可预见的未来将工程化的基于脂质的纳米颗粒转化为临床应用。

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