光动力疗法
化学
光敏剂
多重耐药
细菌
系统间交叉
组合化学
荧光
阳离子聚合
光化学
生物物理学
抗生素
生物化学
生物
有机化学
物理
遗传学
量子力学
核物理学
单重态
激发态
作者
Shaoling Li,Senlin Peng,Shuning Yu,Meiliang Zhi,Xiang Su,Qilong Zhang,Carl Redshaw,Xing Feng
标识
DOI:10.1016/j.dyepig.2024.112388
摘要
Multidrug resistance (MDR) bacterial infection is a serious hazard to human health. Photodynamic therapy (PDT) has been deployed as an emerging tactic to combat pathogenic bacteria, but the development of efficient photosensitizers against MDR bacteria still remains a global challenge. Herein, two near-infrared (NIR) photosensitizers, named TPA-Th and TPA-Ph, which feature aggregation-induced emission (AIE), were constructed and successfully employed for MDR bacteria monitoring and effective elimination. TPA-Th and TPA-Ph exhibited great affinity with MDR G(+) and G(−) bacteria via the electrostatic interaction between the cationic pyridinium segment and the negative bacterial envelope together with hydrophobic forces. Meanwhile, the reinforced D-A effect of the two cationic AIEgens further accelerated the intersystem crossing (ISC) process and enhanced the intramolecular charge transfer (ICT), resulting in the boosted ROS generation capability particularly in the case of predominant hydroxyl radicals. Therefore, superb photodynamic antibacterial performances were achieved for both MRSA and MDR E.coli with a low dose of the AIE photosensitizers. This study provides guidance for the development of high-performance AIE-active PSs with no antibiotic resistance to defeat MDR bacterial infections.
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