材料科学
多重耐药
守护者
纳米技术
微生物学
噬菌体
抗药性
生物
大肠杆菌
有机化学
遗传学
基因
化学
作者
Luojia Chen,Mingyu Wu,Si‐Ling Chen,Rui Hu,Yifei Wang,Weijuan Zeng,Shun Feng,Min Ke,Lianrong Wang,Shi Chen,Meijia Gu
标识
DOI:10.1002/adma.202407268
摘要
Abstract Clinical multidrug‐resistant Pseudomonas aeruginosa (MDR‐PA) is the leading cause of refractory bacterial keratitis (BK). However, the reported BK treatment methods lack biosecurity and bioavailability, which usually causes irreversible visual impairment and even blindness. Herein, for BK caused by clinically isolated MDR‐PA infection, armed phages are modularized with the type I photosensitizer (PS) ACR‐DMT, and an intelligent phage eyedrop is developed for combined phagotherapy and photodynamic therapy (PDT). These eyedrops maximize the advantages of bacteriophages and ACR‐DMT, enabling more robust and specific targeting killing of MDR‐PA under low oxygen‐dependence, penetrating and disrupting biofilms, and efficiently preventing biofilm reformation. Altering the biofilm and immune microenvironments alleviates inflammation noninvasively, promotes corneal healing without scar formation, protects ocular tissues, restores visual function, and prevents long‐term discomfort and pain. This strategy exhibits strong scalability, enables at‐home treatment of ocular surface infections with great patient compliance and a favorable prognosis, and has significant potential for clinical application.
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