核糖核酸
化学
计算生物学
基因敲除
输送系统
RNA干扰
纳米技术
生物化学
基因
生物
药理学
材料科学
作者
Yuebao Zhang,Changzhen Sun,Chang Wang,Katarina E. Jankovic,Yizhou Dong
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-07-19
卷期号:121 (20): 12181-12277
被引量:281
标识
DOI:10.1021/acs.chemrev.1c00244
摘要
RNA-based therapeutics have shown great promise in treating a broad spectrum of diseases through various mechanisms including knockdown of pathological genes, expression of therapeutic proteins, and programmed gene editing. Due to the inherent instability and negative-charges of RNA molecules, RNA-based therapeutics can make the most use of delivery systems to overcome biological barriers and to release the RNA payload into the cytosol. Among different types of delivery systems, lipid-based RNA delivery systems, particularly lipid nanoparticles (LNPs), have been extensively studied due to their unique properties, such as simple chemical synthesis of lipid components, scalable manufacturing processes of LNPs, and wide packaging capability. LNPs represent the most widely used delivery systems for RNA-based therapeutics, as evidenced by the clinical approvals of three LNP-RNA formulations, patisiran, BNT162b2, and mRNA-1273. This review covers recent advances of lipids, lipid derivatives, and lipid-derived macromolecules used in RNA delivery over the past several decades. We focus mainly on their chemical structures, synthetic routes, characterization, formulation methods, and structure-activity relationships. We also briefly describe the current status of representative preclinical studies and clinical trials and highlight future opportunities and challenges.
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