Polymyxin B-targeted liposomal photosensitizer cures MDR A. baumannii burn infections and accelerates wound healing via M1/M2 macrophage polarization

被引:10
|
作者
Cui, Zixin [1 ,2 ]
Li, Yiyang [1 ,2 ]
Qin, Yannan [3 ]
Li, Jianzhou [2 ]
Shi, Lei [2 ]
Wan, Meijuan [2 ]
Hu, Min [4 ]
Chen, Yunru [2 ]
Ji, Yanhong [1 ]
Hou, Yuzhu [1 ]
Liu, Chengcheng [1 ]
Ye, Feng [2 ]
机构
[1] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Pathogen Microbiol & Immunol, Hlth Sci Ctr, 76 West Yanta Rd, Xian 710061, Peoples R China
[2] Xi An Jiao Tong Univ, Dept Infect, Affiliated Hosp 1, 277 West Yanta Rd, Xian 710061, Peoples R China
[3] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Cell Biol & Genet, Hlth Sci Ctr, 76 West Yanta Rd, Xian 710061, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Chem, Dept Chem, 28 Xianning West Rd, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
Multidrug-resistant Acinetobacter baumannii; Burn infections; Polymyxin B-targeted liposomal; photosensitizer; Wound healing; Macrophage polarization; ANTIMICROBIAL PHOTODYNAMIC INACTIVATION; IN-VITRO; THERAPY; SKIN; PHOTOINACTIVATION; ATTACHMENT; FULLERENE; BACTERIA; CHARGE;
D O I
10.1016/j.jconrel.2023.12.046
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multidrug-resistant (MDR) Acinetobacter baumannii infections pose a significant challenge in burn wound management, necessitating the development of innovative therapeutic strategies. In this work, we introduced a novel polymyxin B (PMB)-targeted liposomal photosensitizer, HMME@Lipo-PMB, for precise and potent antimicrobial photodynamic therapy (aPDT) against burn infections induced by MDR A. baumanni. HMME@Lipo-PMBmediated aPDT exhibited enhanced antibacterial efficacy by specifically targeting and disrupting bacterial cell membranes, and generating increased intracellular ROS. Remarkably, even at low concentrations, this targeted approach significantly reduced bacterial viability in vitro and completely eradicated burn infections induced by MDR A. baumannii in vivo. Additionally, HMME@Lipo-PMB-mediated aPDT facilitated burn infection wound healing by modulating M1/M2 macrophage polarization. It also effectively promoted acute inflammation in the early stage, while attenuated chronic inflammation in the later stage of wound healing. This dynamic modulation promoted the formation of granulation tissue, angiogenesis, and collagen regeneration. These findings demonstrate the tremendous potential of HMME@Lipo-PMB-mediated aPDT as a promising alternative for the treatment of burn infections caused by MDR A. baumannii.
引用
收藏
页码:297 / 311
页数:15
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