生物相容性
活性氧
化学
抗氧化剂
超氧化物歧化酶
过氧化氢酶
纳米技术
生物相容性材料
催化作用
氧化应激
谷胱甘肽过氧化物酶
金属有机骨架
过氧化氢
酶
生物物理学
炎症
谷胱甘肽
级联
组合化学
生物化学
人工酶
生物传感器
协同催化
作者
Ruizhen Tian,Hongyin Ma,Jiaxin Ren,Yijia Li,Zherui Zhang,Zhengwei Xu,Lei He,Canhong Zhu,Jiayun Xu,Shuangjiang Yu,Yu Yang,Tingting Wang,Junqiu Liu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-01-05
卷期号:20 (2): 2435-2450
被引量:2
标识
DOI:10.1021/acsnano.5c20015
摘要
Metal-free hydrogen-bonded organic frameworks (HOFs) are porous materials formed via hydrogen bonding of organic building blocks, offering excellent biocompatibility and enzyme compatibility for biomedical applications. However, leveraging HOFs to create multienzyme cascade antioxidant nanozymes for cerebral ischemia-reperfusion injury (CIRI) therapy remains challenging. Here, selenium-containing nano-HOFs (SeHOFs) were synthesized as glutathione peroxidase mimics, encapsulating superoxide dismutase (SOD) and catalase (CAT) enzymes in situ to form a hybrid cascade antioxidant system (SeHOF@CAT@SOD). SeHOFs exhibited enhanced catalytic activity, preserved enzyme functionality, and provided protection against temperature, proteolysis, and denaturation. The metal-free nanozyme demonstrated excellent biocompatibility and cascade catalytic efficacy, scavenging reactive oxygen species and mitigating apoptosis and ferroptosis in vitro. Peptide modifications enhanced infarct site accumulation, effectively reducing infarct volume, oxidative stress, neuronal apoptosis, ferroptosis, and inflammation in CIRI models. This study underscores the potential of nano-HOFs as scaffolds for advanced therapeutic nanozyme development in ischemic stroke treatment.
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