胆酸
鹅去氧胆酸
胆汁酸
胆酸
胆固醇
脱氧胆酸
体内
化学
基因传递
生物化学
转染
生物
基因
生物技术
作者
Savan K. Patel,Margaret M. Billingsley,Alvin J. Mukalel,Ajay S. Thatte,Alex G. Hamilton,Ningqiang Gong,Rakan El‐Mayta,Hannah C. Safford,Maria Merolle,Michael J. Mitchell
出处
期刊:Theranostics
[Ivyspring International Publisher]
日期:2023-10-30
卷期号:14 (1): 1-16
被引量:24
摘要
Lipid nanoparticles (LNPs) have emerged as a viable, clinically-validated platform for the delivery of mRNA therapeutics. LNPs have been utilized as mRNA delivery systems for applications including vaccines, gene therapy, and cancer immunotherapy. However, LNPs, which are typically composed of ionizable lipids, cholesterol, helper lipids, and lipid-anchored polyethylene glycol, often traffic to the liver which limits the therapeutic potential of the platform. Several approaches have been proposed to resolve this tropism such as post-synthesis surface modification or the addition of synthetic cationic lipids.
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