抗菌剂
化学
两亲性
胆汁酸
生物相容性
抗菌肽
细菌
生物膜
组合化学
药品
氨基酸
生物化学
药物输送
微生物学
有机化学
药理学
生物
共聚物
遗传学
聚合物
作者
Caihong Lin,Yushi Wang,Mengqi Le,Kai-Feng Chen,Yong‐Guang Jia
标识
DOI:10.1021/acs.bioconjchem.0c00642
摘要
With the emergence of drug-resistant bacteria and the formation of biofilms by bacteria and fungi, microbial infections gradually threaten global health. Natural antimicrobial peptides (AMPs) have low susceptibility for developing resistance due to the membrane targeted mechanism, but instability and high manufacturing cost limit their applications in clinic. Bile acids, a group of steroids in the human body, with high stability, biocompatibility, and inherent facial amphiphilic structure similar to the characteristics of AMPs, have been applied to the biological field, such as drug delivery systems, self-healing hydrogels, antimicrobials, and so on. In this review, we mainly focus on the different classes of bile acid-based antimicrobials in recent years. Various designs and methods for the preparation of unimolecular antimicrobials with bile acid skeletons are first introduced, including coupling of primary amine, quaternary ammonium, and amino acid units with bile acid skeletons. Some representative oligomeric antimicrobials, including dimers of bile acids, are summarized. Finally, macromolecular antimicrobials bearing some positive charges at the main chain or side chain and interaction mechanisms of these bile acid-based antimicrobials are discussed.
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