Reactive Oxygen Species-Induced Aggregation of Nanozymes for Neuron Injury

被引:31
|
作者
He, Hua [1 ,2 ]
Shi, Xinjian [1 ,2 ]
Wang, Junying [3 ]
Wang, Xiaojuan [1 ,2 ]
Wang, Qian [1 ,2 ]
Yu, Daoyong [1 ,2 ]
Ge, Baosheng [1 ,2 ]
Zhang, Xiaodong [3 ]
Huang, Fang [1 ,2 ]
机构
[1] China Univ Petr East China, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] China Univ Petr East China, Coll Chem Engn, Qingdao 266580, Peoples R China
[3] Tianjin Univ, Sch Sci, Dept Phys, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
nanozyme; catalytic activity; ROS-induced aggregation; organ-targeting; traumatic brain injury; PEROXIDASE-LIKE ACTIVITY; HYDROGEN-PEROXIDE; NANOPARTICLES; BRAIN; GOLD; ENZYME; NEUROINFLAMMATION; MECHANISMS; THERAPIES; CHEMISTRY;
D O I
10.1021/acsami.9b17509
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanozymes show excellent enzyme activity and robust catalytic properties, but the targeting capability to disease organs is limited because of lack of specificity. Herein, we developed an ultrasmall (similar to 3 nm) organic nanozyme that can gradually aggregate under a reactive oxygen species (ROS)-rich environment via a spontaneous reaction, namely, ROS-induced aggregation. The size of nanozymes is 75 and 100 times higher than the original size under (OH)-O-center dot and H2O2 environments without losing enzyme activity. In vitro experiments confirm that nanozymes prefer to aggregate in mitochondria under ROS-rich conditions. Importantly, the nanozymes show in situ ROS-induced aggregation in the brain, similar to 9 times higher uptake than ordinary nanozymes, indicating their potential for treating ROS-related diseases in the central nervous system.
引用
收藏
页码:209 / 216
页数:8
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