Phase separation of extracellular polymeric substances induced by bacteria responsive Nano-Antibiotics for drug-resistant bacterial infection management

被引:8
|
作者
Zhu, Xufeng [1 ,2 ]
Liang, Chunmei [1 ,2 ]
Chen, Jinjun [1 ,2 ]
Gao, Jie [1 ,2 ]
Chen, Weigang [1 ,2 ]
Ouyang, Qianqian [1 ,2 ]
Luo, Lianxiang [1 ,2 ]
Huang, Zunnan
Luo, Hui [1 ,2 ]
Chen, Lanmei [3 ,4 ]
Chen, Jincan [1 ,2 ,3 ,4 ]
机构
[1] Guangdong Med Univ, Marine Biomed Res Inst, Zhanjiang 524023, Guangdong, Peoples R China
[2] Marine Biomed Res Inst Guangdong Zhanjiang, Zhanjiang 524023, Guangdong, Peoples R China
[3] Guangdong Med Univ, Sch Pharm, Key Lab Comp Aided Drug Design Dongguan City, Dongguan 523808, Guangdong, Peoples R China
[4] Guangdong Med Univ, Sch Pharm, Guangdong Key Lab Res & Dev Nat Drugs, Zhanjiang 524023, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Iridium complex; Pazufloxacin; Extracellular Polymeric Substances; Phase separation; Biofilm infection;
D O I
10.1016/j.cej.2023.148136
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Bacterial quorum sensing (QS) and bacterial extracellular polymeric substances (EPS) are the major challenges in treating biofilm chronic infection. Herein, we proposed targeting intervention phase separation of EPS by nanoantibiotics (Ir(ppy)2dmb-PAZ-HA) as an effective strategy for combating bacterial biofilm infection, in which Iridium complex (Ir(ppy)2dmb-CHO) and antibiotic (Pazufloxacin, PAZ) for synergistic antibacterial, and hyaluronic acid (HA) was used to enhance Ir(ppy)2dmb-PAZ release on-demand in biofilm microenvironment. In vitro results showed that Ir(ppy)2dmb-PAZ-HA holds excellent antibacterial activity and antibiofilm capacity. Importantly, Ir(ppy)2dmb-PAZ-HA can be target to regulate phase separation of EPS, and then interfere with biofilm formation, which is a competitive mechanism between Ir(ppy)2dmb-PAZ-HA and Methicillin-resistant Staphylococcus aureus (MRSA) itself. In addition, in vivo results confirmed that Ir(ppy)2dmb-PAZ-HA was able to accelerate biofilm chronic wound healing, and effectively alleviate bacterial acute lung infection. Accordingly, this study provides a new antibiofilm target, and provides a novel idea for the design of small molecular metal antibacterial drugs and antibiotic reuse.
引用
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页数:17
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