催化作用
过氧化氢酶
超氧化物歧化酶
吸附
活性氧
协调球
光化学
组合化学
化学
酶
金属
有机化学
生物化学
作者
Shiyu Xu,Yuan Yin,Yukun Pan,Huihui Zhang,Siyuan Yin,Xinya Zhang,Yayun Zhang,Sheng Dai,Huawei Shen,Yongsheng Li,Dechao Niu
出处
期刊:Small
[Wiley]
日期:2025-06-04
卷期号:21 (31): e2502896-e2502896
被引量:1
标识
DOI:10.1002/smll.202502896
摘要
Abstract The unsaturated coordination alters the electronic structure of metal atoms, exposing more active sites, and thereby demonstrating high catalytic activity. It is extremely difficult to precisely regulate the unsaturated coordination environment of single‐atom catalysts due to the thermodynamically unstable structure. Herein, a facile “micelle‐confined oxidative crosslinking and coupled coordination” strategy is proposed to construct a copper single‐atom catalyst with an unsaturated Cu‐N 2 coordination structure in a confined silica‐carbon framework (Cu SA@MCSN), which demonstrate unique pH‐dependent multiple‐enzymatic activity (peroxidase (POD)‐like activity in an acidic environment with a low K m of 6.9 mM and V max of 6.3 × 10 −8 M s −1 and superoxide dismutase (SOD)‐ and catalase (CAT)‐like activity under neutral conditions). Density functional theory calculations also further confirm that the asymmetric Cu‐N 2 sites with edge configurations exhibit a strong adsorption capacity for oxygen‐containing intermediates showing a faster reaction rate compared to their saturated coordination structure. More importantly, the metformin (MET)‐loaded Cu SA@MCSN demonstrates multi‐pathway antibacterial ability in acidic microenvironments and long‐term anti‐inflammatory effects in neutral microenvironments through the downregulation of pro‐inflammatory factors and the up‐regulation of anti‐inflammatory and tissue regeneration factors on a rat model of methicillin‐resistant Staphylococcus aureus (MRSA)‐infected diabetic wounds.
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