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用于RNA递送的仿生脂质纳米载体

Bioinspired Lipid Nanocarriers for RNA Delivery.

作者信息

Golubovic Alex, Tsai Shannon, Li Bowen

机构信息

Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 3M2, Canada.

Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario M5S 3G9, Canada.

出版信息

ACS Bio Med Chem Au. 2023 Jan 16;3(2):114-136. doi: 10.1021/acsbiomedchemau.2c00073. eCollection 2023 Apr 19.

Abstract

RNA therapy is a disruptive technology comprising a rapidly expanding category of drugs. Further translation of RNA therapies to the clinic will improve the treatment of many diseases and help enable personalized medicine. However, in vivo delivery of RNA remains challenging due to the lack of appropriate delivery tools. Current state-of-the-art carriers such as ionizable lipid nanoparticles still face significant challenges, including frequent localization to clearance-associated organs and limited (1-2%) endosomal escape. Thus, delivery vehicles must be improved to further unlock the full potential of RNA therapeutics. An emerging strategy is to modify existing or new lipid nanocarriers by incorporating bioinspired design principles. This method generally aims to improve tissue targeting, cellular uptake, and endosomal escape, addressing some of the critical issues facing the field. In this review, we introduce the different strategies for creating bioinspired lipid-based RNA carriers and discuss the potential implications of each strategy based on reported findings. These strategies include incorporating naturally derived lipids into existing nanocarriers and mimicking bioderived molecules, viruses, and exosomes. We evaluate each strategy based on the critical factors required for delivery vehicles to succeed. Finally, we point to areas of research that should be furthered to enable the more successful rational design of lipid nanocarriers for RNA delivery.

摘要

RNA疗法是一种颠覆性技术,包含一类迅速扩展的药物。将RNA疗法进一步转化应用于临床将改善多种疾病的治疗,并有助于实现个性化医疗。然而,由于缺乏合适的递送工具,RNA的体内递送仍然具有挑战性。当前最先进的载体,如可电离脂质纳米颗粒,仍然面临重大挑战,包括频繁定位于与清除相关的器官以及有限的(1%-2%)内体逃逸率。因此,必须改进递送载体,以进一步释放RNA疗法的全部潜力。一种新兴策略是通过纳入受生物启发的设计原则来修饰现有的或新型的脂质纳米载体。这种方法通常旨在改善组织靶向性、细胞摄取和内体逃逸,解决该领域面临的一些关键问题。在这篇综述中,我们介绍了创建受生物启发的基于脂质的RNA载体的不同策略,并根据已报道的研究结果讨论了每种策略的潜在影响。这些策略包括将天然衍生的脂质纳入现有的纳米载体以及模仿生物衍生分子、病毒和外泌体。我们根据递送载体成功所需的关键因素评估每种策略。最后,我们指出了为实现更成功的用于RNA递送的脂质纳米载体的合理设计而应进一步开展研究的领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f72/10125326/ab127fc3636e/bg2c00073_0001.jpg

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