核糖核酸
免疫原性
外体
微泡
药物输送
遗传增强
计算生物学
医学
纳米技术
生物
小RNA
基因
免疫系统
免疫学
材料科学
遗传学
作者
Yao Lu,Wei Huang,Meng Li,Aiping Zheng
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-02-10
卷期号:15 (2): 598-598
被引量:9
标识
DOI:10.3390/pharmaceutics15020598
摘要
In the last few decades, RNA-based drugs have emerged as a promising candidate to specifically target and modulate disease-relevant genes to cure genetic defects. The key to applying RNA therapy in clinical trials is developing safe and effective delivery systems. Exosomes have been exploited as a promising vehicle for drug delivery due to their nanoscale size, high stability, high biocompatibility, and low immunogenicity. We reviewed and summarized the progress in the strategy and application of exosome-mediated RNA therapy. The challenges of exosomes as a carrier for RNA drug delivery are also elucidated in this article. RNA molecules can be loaded into exosomes and then delivered to targeted cells or tissues via various biochemical or physical approaches. So far, exosome-mediated RNA therapy has shown potential in the treatment of cancer, central nervous system disorders, COVID-19, and other diseases. To further exploit the potential of exosomes for RNA delivery, more efforts should be made to overcome both technological and logistic problems.
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