Mixed valence state cerium metal organic framework with prominent oxidase-mimicking activity for ascorbic acid detection: Mechanism and performance

抗坏血酸 化学 检出限 吸光度 氧化还原 价(化学) 电子顺磁共振 普鲁士蓝 氧化酶试验 金属 催化作用 选择性 铁氰化物 无机化学 核化学 光化学 电化学 电极 物理化学 有机化学 色谱法 核磁共振 物理 食品科学
作者
Manjun Fu,Fang Xu,Juntao Yan,Chunlei Wang,Guozhi Fan,Guangsen Song,Bo Chai
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:641: 128610-128610 被引量:42
标识
DOI:10.1016/j.colsurfa.2022.128610
摘要

It is indispensable to establish a simple, effective and accurate method for ascorbic acid (AA) detection since it plays a crucial role in human health. Herein, a novel oxidase mimic of mixed valence state cerium metal organic framework (MVCM) was successfully synthesized by in-situ partial oxidation of cerium metal organic framework (Ce-MOF). On account of the Ce (Ⅲ)/Ce (Ⅳ) redox couple inside, MVCM could directly catalyze the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) to generate a blue color product (ox TMB) without adding H2O2, exhibiting a prominent intrinsic oxidase mimetic activity compared to Ce-MOF. Moreover, this catalytic mechanism of MVCM was further clarified by means of cyclic voltammetry (CV) test, UV–vis absorption spectra with O2 or N2 saturated condition and electron paramagnetic resonance (EPR) measurements. In the presence of AA, a redox reaction occurred between AA and ox TMB, and then resulting in a conspicuous blue color fading. By optimizing the testing conditions, a linear absorbance response was well correlated with the AA concentration ranging from 20 to 500 μM with a detection limit of 3.57 μM. MVCM also displayed the excellent selectivity and anti-interference performance for AA detection. Benefitting from the above, this AA detection method was applied in real Vitamin C effervescent tablets, showing a favorable reproducibility and feasibility. These results strongly indicated that the proposed method based on MVCM as an oxidase mimic might be a promising candidate for AA detection in food field.
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