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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.
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页码:209 / 216
页数:8
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