Lattice‐Reconstructed Ru‐Clusters on FeOOH‐Based Self‐Adaptive Artificial Peroxisome with Programmed ROS Regulation for Infectious and Inflammatory Chronic Wounds

炎症 活性氧 氧化应激 慢性伤口 过氧化物酶体 伤口愈合 耐火材料(行星科学) 氧化磷酸化 体内 癌症研究 炎症反应 免疫学 细胞生物学 材料科学 生物信息学 生物 医学 细胞代谢 药理学 过氧化物酶体增殖物激活受体 金黄色葡萄球菌 新陈代谢 细菌
作者
Heng Yang,Xiaoke Jia,Ting Wang,Jiangge Li,Wei Geng,Mohsen Adeli,Tian Ma,Yang Gao,Chong Cheng,Weifeng Zhao
出处
期刊:Advanced Materials [Wiley]
卷期号:38 (9): e20395-e20395 被引量:3
标识
DOI:10.1002/adma.202520395
摘要

Chronic refractory wounds present substantial clinical difficulties, owing to their complex wound microenvironments featuring bacterial colonization, sustained inflammation, and deficient angiogenesis. Existing treatment options often fall short of concurrently overcoming these interconnected obstacles, underscoring the demand for integrated therapeutic platforms that combine antimicrobial, anti-inflammatory, and pro-angiogenic properties. Drawing inspiration from natural peroxisomes, a lattice-reconstructed Ru-clusters are designed on FeOOH-based self-adaptive artificial peroxisome with programmed reactive oxygen species (ROS) regulation for infectious and inflammatory chronic wounds. Within this architecture, electron-rich Ru clusters and hole-rich FeOOH domains establish an efficient electron-transfer network. Density functional theory calculations demonstrate that this distinctive electronic structure lowers reaction energy barriers, enabling pH-switchable ROS-catalytic behaviors. Under acidic wound pH, LR-RuC@FeOOH catalyzes ROS generation to disrupt bacterial metabolism and eliminate infections, while under neutral conditions, it efficiently scavenges ROS to alleviate oxidative stress and support tissue repair, enabling a logically sequenced therapeutic progression from infection control to inflammation resolution. In vivo experiments using diabetic foot ulcers confirmed that LR-RuC@FeOOH significantly enhanced bacterial clearance, attenuated inflammatory responses, stimulated neovascularization, and accelerated wound closure. These results position LR-RuC@FeOOH as an artificial peroxisome with stage-specific therapies and promising translational potential for the treatment of refractory diabetic wounds and other infection-related pathologies.
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