支柱
生物膜
化学
组合化学
内分泌干扰物
环境化学
生物化学
内分泌系统
遗传学
结构工程
激素
生物
工程类
细菌
作者
Shuwen Guo,Qiaoxian Huang,Yuan Chen,Jianwen Wei,Jun Zheng,Leyong Wang,Yitao Wang,Ruibing Wang
标识
DOI:10.1002/anie.202013975
摘要
Due to the inherent resistance of bacterial biofilms to antibiotics and their serious threat to global public health, novel therapeutic agents and strategies to tackle biofilms are urgently needed. To this end, we designed and synthesized a novel guanidinium-functionalized pillar[5]arene (GP5) that exhibited high antibacterial potency against Gram-negative E. coli (BH101) and Gram-positive S. aureus (ATCC25904) strains. More importantly, GP5 effectively disrupted preformed E. coli biofilms by efficient penetration through biofilm barriers and subsequent destruction of biofilm-enclosed bacteria. Furthermore, host-guest complexation between GP5 and cefazolin sodium, a conventional antibiotic that otherwise shows negligible activity against biofilms, exhibited much enhanced, synergistic disruption activity against E. coli biofilms, thus providing a novel supramolecular platform to effectively disrupt biofilms.
科研通智能强力驱动
Strongly Powered by AbleSci AI