Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, United States.
Department of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, SC, 29209, United States.
Biomaterials. 2023 Oct;301:122275. doi: 10.1016/j.biomaterials.2023.122275. Epub 2023 Aug 12.
Inspired by the facial amphiphilic nature and antimicrobial efficacy of many antimicrobial peptides, this work reported facial amphiphilic bicyclic naphthoic acid derivatives with different ratios of charges to rings that were installed onto side chains of poly(glycidyl methacrylate). Six quaternary ammonium-charged (QAC) polymers were prepared to investigate the structure-activity relationship. These QAC polymers displayed potent antibacterial activity against various multi-drug resistant (MDR) gram-negative pathogens such as Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. Polymers demonstrated low hemolysis and high antimicrobial selectivity. Additionally, they were able to eradicate established biofilms and kill metabolically inactive dormant cells. The membrane permeabilization and depolarization results indicated a mechanism of action through membrane disruption. Two lead polymers showed no resistance from MDR-P. aeruginosa and MDR-K. pneumoniae. These facial amphiphiles are potentially a new class of potent antimicrobial agents to tackle the antimicrobial resistance for both planktonic and biofilm-related infections.
受许多抗菌肽的面部两亲性和抗菌功效的启发,本工作报道了具有不同电荷与环比的面部两亲性双环萘酸衍生物,这些衍生物被安装在聚(甲基丙烯酸缩水甘油酯)的侧链上。制备了六种季铵盐电荷(QAC)聚合物以研究结构-活性关系。这些 QAC 聚合物对各种多药耐药(MDR)革兰氏阴性病原体(如大肠杆菌、铜绿假单胞菌、肺炎克雷伯菌和鲍曼不动杆菌)具有很强的抗菌活性。聚合物表现出低溶血和高抗菌选择性。此外,它们能够根除已建立的生物膜并杀死代谢不活跃的休眠细胞。膜通透性和去极化结果表明其作用机制是通过破坏细胞膜。两种先导聚合物对 MDR-P. aeruginosa 和 MDR-K. pneumoniae 没有耐药性。这些两亲性化合物有可能成为一类新的强效抗菌剂,用于解决与浮游生物和生物膜相关感染有关的抗菌耐药性问题。