药品
核酸
药物输送
化学
组合化学
葫芦素
纳米技术
表征(材料科学)
靶向给药
生物化学
有机化学
材料科学
药理学
超分子化学
生物
分子
作者
Rajesh Kishore Kumar Sanku,Ozlem Ozen Karakus,Monica Ilies,Marc A. Ilies
出处
期刊:Acs Symposium Series
[American Chemical Society]
日期:2019-01-01
卷期号:: 187-221
被引量:15
标识
DOI:10.1021/bk-2019-1309.ch009
摘要
Host–guest complexation based on non-covalent interactions can be successfully exploited for drug and nucleic acid delivery purposes. The chapter covers the main classes of hosts used for these applications, namely cyclodextrins, calixarenes, and cucurbiturils and reveals the main representatives and their physicochemical characteristics that modulate the complexation process. It also highlights relevant drugs and nucleic acid complexes, together with the dysfunctions and diseases where the host–guest complexes have been successfully used.
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