Loaded endogenous CO mimetic nanomedicine mitigates ischemic stroke ischemia-reperfusion injury

被引:0
|
作者
Ma, Jing [1 ,2 ,3 ]
Tian, Yu [1 ,2 ,3 ]
Chen, Yibiao [1 ,2 ,3 ]
Zhang, Xiaodan [1 ,2 ,3 ]
Ding, Chenyu [1 ,2 ,3 ]
Lin, Zhangya [1 ,2 ,3 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Neurosurg Res Inst, Dept Neurosurg, Fuzhou 350005, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Neurosurg, Binhai Campus, Fuzhou 350212, Fujian, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp 1, Fujian Prov Inst Brain Disorders & Brain Sci, Fuzhou 350005, Fujian, Peoples R China
关键词
Ischemic stroke; Ischemia-reperfusion injury; Carbon monoxide; Nanoparticle; Macrophage membrane; Ferroptosis; ACTIVATION;
D O I
10.1016/j.colcom.2025.100820
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ischemia-reperfusion injury is a major threat in ischemic stroke, with limited treatment options. Edaravone, a first-line drug, has multiple limitations, and the narrow time window for reperfusion therapy complicates treatment. This study reports a nanoparticle drug designed to mitigate ischemia-reperfusion injury by targeting inflammation. The drug is made of mesoporous silica (SiO2) loaded with the CO-releasing molecule CORM-401 and coated with a macrophage membrane (MM) shell. The nanoparticles effectively cross the blood-brain barrier and target ischemic brain lesions. In vitro and in vivo studies show that SiO2@MM@CORM-401 scavenges reactive oxygen species (ROS), promotes anti-inflammatory factor release, and inhibits pro-inflammatory factors. Additionally, CO helps prevent ferroptosis in the ischemic penumbra, offering a potential mechanism for alleviating ischemic stroke and providing a novel therapeutic approach.
引用
收藏
页数:10
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