Modulation of the biocatalytic activity and selectivity of CeO2 nanozymes via atomic doping engineering

被引:23
|
作者
Zhang, Shaofang [1 ]
Ruan, Haiyan [2 ,3 ]
Xin, Qi [1 ]
Mu, Xiaoyu [1 ]
Wang, Hao [1 ]
Zhang, Xiao-Dong [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Acad Med Engn & Translat Med, Tianjin Key Lab Brain Sci & Neural Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Sci, Dept Phys, Tianjin 300350, Peoples R China
[3] Tianjin Univ, Sch Sci, Tianjin Key Lab Low Dimens Mat Phys & Preparing Te, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-ATOM; MIMETIC ACTIVITY; NANOPARTICLES; DISEASE; CATALYSIS; OXYGEN;
D O I
10.1039/d2nr05742e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Artificial enzymes show prospects in biomedical applications due to their stable enzymatic catalytic activity and ease of preparation. CeO2 nanozymes represent a versatile platform showing multiple enzyme-mimicking activities, although their biocatalytic activities and selectivity are relatively poor for biomedical use. Herein, we developed Mn- and Co-doped CeO2 nanozymes (M/CeO2, M = Mn or Co) via atomic engineering to achieve a significant increase in enzyme-like activity. The M/CeO2 nanozymes exhibited outstanding peroxidase-like activity with a reaction rate about 8-10 times higher than that of CeO2. Importantly, the Co/CeO2 nanozyme preferred for catalase-like activity with a 4-6-fold higher catalytic rate than CeO2, while the Mn/CeO2 nanozyme had a predilection for improving the superoxide dismutase-like capacity. This indicated the selective modulation of enzyme-mimicking activities via atomic doping engineering. Cellular level experiments revealed the in vitro therapeutic effects of the nanozymes. Mn/CeO2 and Co/CeO2 selectively modulated the intracellular redox imbalance in lipopolysaccharide (LPS)- or H2O2-stimulated nerve cells and improved cell survival. This work provides a feasible strategy for the design of catalytically selective artificial enzymes and facilitates the widespread application of CeO2 nanozymes in redox-related diseases.
引用
收藏
页码:4408 / 4419
页数:12
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