The peroxidase-like catalytic activity of in situ prepared cobalt carbonate and its applications in colorimetric detection of hydrogen peroxide, glucose and ascorbic acid

过氧化氢 抗坏血酸 过氧化物酶 催化作用 化学 辣根过氧化物酶 基质(水族馆) 核化学 过氧化物 无机化学 组合化学 生物化学 有机化学 食品科学 地质学 海洋学
作者
Li‐Jing Peng,Chunyan Zhang,Weiyi Zhang,Hang‐Yu Zhou,Feng Yang
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:651: 129744-129744 被引量:16
标识
DOI:10.1016/j.colsurfa.2022.129744
摘要

In this study, the cobalt carbonate (CoCO3) was in situ prepared using cobalt (Ⅱ) and carbonate at room temperature, and the intrinsic peroxidase-like activity of CoCO3 was demonstrated for the first time through the oxidation of chromogenic substrate 3, 3', 5, 5' - tetramethylbenzidine (TMB) in the presence of hydrogen peroxide (H2O2). The effects of pH, reaction temperature, and incubation time on the catalytic activity of CoCO3 were studied. Under the optimal reaction conditions, the Michaelis constant (Km) of CoCO3 to H2O2 is 0.443 mM, which is lower than that of natural horseradish peroxidase and the previously reported peroxidase mimics. Furthermore, the mechanism exploration experiments confirm that the catalytic activity of CoCO3 is mainly attributed to the hydroxyl radical (•OH). Finally, based on the outstanding peroxidase-like activity of CoCO3, a colorimetric sensor for the detection of H2O2, glucose, and ascorbic acid (AA) was developed, which shows satisfactory selectivity and recovery. In addition, the total antioxidant capacity of three types of tea, dried lemon, three kinds of fresh fruit juice, and vitamin C tablet were determined. In short, this study reports a novel in situ generated CoCO3, which can be prepared rapidly at room temperature, eliminating the harsh, cumbersome, and time-consuming synthesis and purification process. The developed sensor based on the newly found excellent peroxidase-like activity of in situ prepared CoCO3 for the determination of H2O2, glucose, and AA is fast, simple, low cost, and high sensitivity.
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