活性氧
光热治疗
炎症
伤口愈合
过氧化氢酶
超氧化物歧化酶
材料科学
缺氧(环境)
微生物学
细胞生物学
生物
免疫学
化学
纳米技术
酶
氧气
生物化学
有机化学
作者
Wentao Wang,Yumeng Gao,Wang Xu,Yan Xu,Ninglin Zhou,Yuanyuan Li,Ming Zhang,Ben Zhong Tang
标识
DOI:10.1002/adma.202307785
摘要
Abstract Chronic wounds caused by bacterial infections are a major challenge in medical fields. The hypoxia condition extremely induces reactive oxygen species (ROS) generation and upregulates the expression of hypoxia‐inducible factor, both of which can increase the pro‐inflammatory M1 subtype macrophages production while reducing the anti‐inflammatory M2 subtype macrophages. Besides, bacteria‐formed biofilms can hinder the penetration of therapeutic agents. Encouraged by natural motors automatically executing tasks, hypothesized that supplying sufficient oxygen (O 2 ) would simultaneously drive therapeutic agent movement, rescue the hypoxic microenvironment, and disrupt the vicious cycle of inflammation. Here, small organic molecule‐based nanoparticles (2TT‐mC6B@Cu 5.4 O NPs) that possess high photothermal conversion efficiency and enzymatic activities are developed, including superoxide dismutase‐, catalase‐, and glutathione peroxidase‐like activity. 2TT‐mC6B@Cu 5.4 O NPs exhibit superior ROS‐scavenging and O 2 production abilities that synergistically relieve inflammation, alleviate hypoxia conditions, and promote their deep penetration in chronic wound tissues. Transcriptome analysis further demonstrates that 2TT‐mC6B@Cu5.4O NPs inhibit biological activities inside bacteria. Furthermore, in vivo experiments prove that 2TT‐mC6B@Cu 5.4 O NPs‐based hyperthermia can effectively eliminate bacteria in biofilms to promote wound healing.
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