化学
碳化
镁
电子转移
核化学
检出限
氧化酶试验
金属
催化作用
无机化学
酶
色谱法
光化学
物理化学
有机化学
吸附
作者
Yuejie Hou,Yuwan Lu,Xiaodan Zhang,Yuming Huang
标识
DOI:10.1016/j.snb.2022.132409
摘要
Transition metal-based N-doped carbon nanozymes have received great attentions recently, while rare study is on the main group metal-based ones. Here, we designed the N-doped porous carbon with active magnesium sites (Mg/NC) via carbonizing Mg-MOF precursor. The optimized Mg/NC-0.8 displayed a sheet structure. The doping of N and Mg reduced the diffusion and electron transfer resistance, accelerated electron transfer rate, and finally boosted the catalytic activity. The Mg/NC-0.8 showed superior oxidase-like activity capable of significantly promoting 3,3′,5,5′-tetramethylbenzidine (TMB) oxidation. Relative to that of N-doped carbon (NC), the oxidase-like activity of the Mg/NC-0.8 increased by 10.94-fold. The mechanism study showed the generation of O2•−, 1O2 and •OH during Mg/NC-0.8 catalyzed TMB oxidation. The Mg/NC-0.8 displayed good affinity to TMB with a Km value of 0.169 mM. In terms of its high oxidase mimic activity, a sensitive and selective assay for detecting acetylcholinesterase (AChE) activity was set up via restraining TMB oxidation by thiocholine, which was from the AChE-induced hydrolysis of acetylthiocholine. The assay shows a linear concentration range of 0.0001 – 1 U L−1 AChE, with a detection limit of 1 × 10–4 U L−1. It was used to measure AChE activity in real samples.
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