Gautam Aryan, Sasmal Pijus K
School of Physical Sciences, Jawaharlal Nehru University, New Delhi 110067, India.
Inorg Chem. 2025 Feb 17;64(6):2905-2918. doi: 10.1021/acs.inorgchem.4c05064. Epub 2025 Jan 31.
Antibiotic resistance caused by Gram-positive bacteria is a growing global human health threat. Selective discrimination and eradication of Gram-positive bacteria and their biofilms is challenging. Therapeutic strategies with multiple modes of action are urgently needed to address the increase in Gram-positive bacteria-resistant nosocomial infections. In this work, we have presented rationally designed aggregation-induced emission (AIE)-active cationic cyclometalated iridium(III) complexes derived from 2-phenylquinoline and 2,2'-bipyridine ligands for Gram-positive antibacterial studies. The AIE properties of these complexes were exploited for selective discrimination between Gram-positive and Gram-negative bacteria. These complexes displayed good antimicrobial activity against critical Gram-positive ESKAPE pathogens with minimum inhibitory concentrations in the low micromolar range but were inactive against Gram-negative pathogens. Importantly, the complexes can inhibit biofilm formation and eradicate bacteria from mature biofilms, which are major causes of persistent infections and antibiotic resistance and are more difficult to eliminate. In addition, these complexes showed low hemolytic activity against mammalian cells and a high therapeutic index, indicating good selectivity. Interestingly, the complexes kill bacteria through a variety of modes of mechanism, including ROS generation, cell membrane disruption, and depolarization and the loss of bacterial membrane integrity. These findings offer opportunities for designing metal AIEgens to treat Gram-positive bacterial infections effectively.
革兰氏阳性菌引起的抗生素耐药性对全球人类健康构成了日益严重的威胁。选择性区分和根除革兰氏阳性菌及其生物膜具有挑战性。迫切需要具有多种作用模式的治疗策略来应对革兰氏阳性菌耐药性医院感染的增加。在这项工作中,我们展示了合理设计的、由2-苯基喹啉和2,2'-联吡啶配体衍生的聚集诱导发光(AIE)活性阳离子环金属化铱(III)配合物,用于革兰氏阳性菌抗菌研究。利用这些配合物的AIE特性来选择性区分革兰氏阳性菌和革兰氏阴性菌。这些配合物对关键的革兰氏阳性ESKAPE病原体表现出良好的抗菌活性,最低抑菌浓度在低微摩尔范围内,但对革兰氏阴性病原体无活性。重要的是,这些配合物可以抑制生物膜形成并从成熟生物膜中根除细菌,而生物膜是持续性感染和抗生素耐药性的主要原因,且更难消除。此外,这些配合物对哺乳动物细胞表现出低溶血活性和高治疗指数,表明具有良好的选择性。有趣的是,这些配合物通过多种作用机制杀死细菌,包括活性氧生成、细胞膜破坏、去极化以及细菌膜完整性丧失。这些发现为设计金属AIEgens有效治疗革兰氏阳性菌感染提供了机会。