两亲性
抗菌剂
抗菌肽
阳离子聚合
抗生素
大肠杆菌
微生物学
抗菌活性
体内
抗生素耐药性
细菌
组合化学
材料科学
化学
生物化学
生物
聚合物
有机化学
共聚物
高分子化学
遗传学
生物技术
基因
作者
Caihong Lin,Zunwei Ma,Yunpeng Gao,Mengqi Le,Zhifeng Shi,Dawei Qi,Jian-Chao Ma,Zhong‐Kai Cui,Lin Wang,Yong‐Guang Jia
标识
DOI:10.1021/acsami.3c06424
摘要
Antibiotic-resistant bacterial infections have led to an increased demand for antibacterial agents that do not contribute to antimicrobial resistance. Antimicrobial peptides (AMPs) with the facially amphiphilic structures have demonstrated remarkable effectiveness, including the ability to suppress antibiotic resistance during bacterial treatment. Herein, inspired by the facially amphiphilic structure of AMPs, the facially amphiphilic skeletons of bile acids (BAs) are utilized as building blocks to create a main-chain cationic bile acid polymer (MCBAP) with macromolecular facial amphiphilicity via polycondensation and a subsequent quaternization. The optimal MCBAP displays an effective activity against Gram-positive methicillin-resistant Staphylococcus aureus (MRSA) and Gram-negative Escherichia coli, fast killing efficacy, superior bactericidal stability in vitro, and potent anti-infectious performance in vivo using the MRSA-infected wound model. MCBAP shows the low possibility to develop drug-resistant bacteria after repeated exposure, which may ascribe to the macromolecular facial amphiphilicity promoting bacterial membrane disruption and the generation of reactive oxygen species. The easy synthesis and low cost of MCBAP, the superior antimicrobial performance, and the therapeutic potential in treating MRSA infection altogether demonstrate that BAs are a promising group of building blocks to mimic the facially amphiphilic structure of AMPs in treating MRSA infection and alleviating antibiotic resistance.
科研通智能强力驱动
Strongly Powered by AbleSci AI