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含苯磺酰基吲哚衍生物的多靶点抗菌钌基金属药物:合成及其对革兰氏阳性菌和阴性菌的疗效

Multi-target antibacterial Ru-based metallodrugs containing phenylsulfonyl indole derivatives: synthesis and their efficacy against Gram-positive and -negative bacteria.

作者信息

Lin Shijie, Yu Guangying, Zhang Liu, Liao Xiangwen, Jiang Guijuan, Liu Lianghong

机构信息

Department of Pharmacy, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University) Haikou 570311 China.

School of Pharmacy, Jiangxi Science & Technology Normal University Nanchang 330013 China

出版信息

RSC Adv. 2025 Jun 23;15(27):21284-21299. doi: 10.1039/d5ra03098f.

DOI:10.1039/d5ra03098f
PMID:40556701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12184327/
Abstract

The escalating crisis of antimicrobial resistance (AMR) underscores the critical need for the development of novel antibacterial drugs with unique mechanisms of action. Herein, a series of phenylsulfonyl indole-modified Ru-based metallodrugs with multi-target antibacterial mechanisms were prepared and evaluated. Notably, all these complexes showed strong bacteriostatic efficacy against (), and the most active complex, RuS2, showed a lower MIC than that of many common antibiotics. Importantly, RuS2 also showed robust bactericidal efficacy against Gram-negative bacteria () in the presence of subinhibitory concentrations of polymyxin B. In addition, complex RuS2 can reduce bacterial pathogenicity by inhibiting hemolysin secretion and biofilm formation. More importantly, RuS2 can curb the production of drug-resistant bacteria and has significant activity against clinically isolated resistant bacteria. Mechanism studies have demonstrated that RuS2 can destroy the bacterial membrane, cause membrane depolarization, and induce the production of reactive oxygen species (ROS). Finally, the wax worms and mouse infection models confirm that RuS2 has low toxicity and significant anti-infective potency . Taken together, the results presented herein pave a promising way for combating Gram-positive and -negative bacterial infections.

摘要

不断升级的抗菌药物耐药性(AMR)危机凸显了开发具有独特作用机制的新型抗菌药物的迫切需求。在此,制备并评估了一系列具有多靶点抗菌机制的苯基磺酰基吲哚修饰的钌基金属药物。值得注意的是,所有这些配合物对()均表现出强大的抑菌效果,活性最强的配合物RuS2的最低抑菌浓度(MIC)低于许多常用抗生素。重要的是,在亚抑菌浓度的多粘菌素B存在下,RuS2对革兰氏阴性菌()也表现出强大的杀菌效果。此外,配合物RuS2可通过抑制溶血素分泌和生物膜形成来降低细菌致病性。更重要的是,RuS2可抑制耐药菌的产生,对临床分离的耐药菌具有显著活性。机制研究表明,RuS2可破坏细菌膜、导致膜去极化并诱导活性氧(ROS)的产生。最后,蜡虫和小鼠感染模型证实RuS2具有低毒性和显著的抗感染效力。综上所述,本文呈现的结果为对抗革兰氏阳性和阴性细菌感染开辟了一条有前景的道路。

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