败血症
细菌
肺炎链球菌
菌血症
微生物学
抗生素
全身炎症
过氧化氢
全身给药
医学
炎症
化学
免疫学
生物
体内
有机化学
生物技术
遗传学
作者
Yi Wu,Wei Jiang,Shaohu Huo,Shuya Li,Youcui Xu,Shenggang Ding,Jing Zhou,Hang Liu,Wei‐Fu Lv,Yucai Wang
出处
期刊:Biomaterials
[Elsevier]
日期:2021-11-03
卷期号:279: 121237-121237
被引量:23
标识
DOI:10.1016/j.biomaterials.2021.121237
摘要
As a vital bacteria-secreted toxin, hydrogen peroxide (H2O2) can destroy infected tissues and increase vascular permeability, leading to life-threatening systemic bacteremia or sepsis. No strategy that can alleviate H2O2-induced injury and prevent systemic sepsis has been reported. Herein, as a proof of concept, we demonstrate the use of H2O2-reactive metal-organic framework nanosystems (MOFs) for treating H2O2-secreting bacteria. In mice infected with Streptococcus pneumoniae (S. pneumoniae) isolated from patients, MOFs efficiently accumulate in the lungs after systemic administration due to infection-induced alveolar-capillary barrier dysfunction. Moreover, MOFs sequester pneumococcal H2O2, reduce endothelial DNA damage, and prevent systemic dissemination of bacteria. In addition, this nanosystem exhibits excellent chemodynamic bactericidal effects against drug-resistant bacteria. Through synergistic therapy with the antibiotic ampicillin, MOFs eliminate over 98% of invading S. pneumoniae, resulting in a survival rate of greater than 90% in mice infected with a lethal dose of S. pneumoniae. This work opens up new paths for the clinical treatment of toxin-secreting bacteria.
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