纳米载体
清脆的
计算机科学
计算生物学
药物输送
纳米技术
核酸酶
材料科学
生物
基因
遗传学
作者
Yan Lyu,Cheng Yang,Xiaomei Lyu,Kanyi Pu
出处
期刊:Small
[Wiley]
日期:2021-03-24
卷期号:17 (24): e2005222-e2005222
被引量:20
标识
DOI:10.1002/smll.202005222
摘要
Abstract Among programmable nuclease‐based genome editing tools, the clustered regularly interspaced short palindromic repeats (CRISPR) system with accuracy and the convenient operation is most promising to be applied in gene therapy. The development of effective delivery carriers for the CRISPR system is the major premise to achieve practical applications. Although many nanocarrier‐mediated deliveries have been reported to be safer and cheaper over the physical and viral delivery, the accumulation at disease sites or controllability with the spatial or temporal resolution are still desired on nanocarriers to reduce side effects and off‐target from the CRISPR system. Therefore, the targetable and controllable nanocarriers to actively deliver the CRISPR system are summarized. The cell or even organ selective nanocarriers are introduced first, followed by the discussion of nanocarriers controlled by biochemical or physical signals. At last, the potential challenges faced by existing nanocarriers are discussed.
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