基于 AgCuO/Cu2O 纳米酶的比色法和光电化学双模型策略用于检测血清中的 Hg2+

Xinxin Gu, Tao Cheng, Tairu Yin, Xiaoyu Guo, Xinling Liu, Ying Wen, Haifeng Yang, Yiping Wu
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引用次数: 0

摘要

制备了一种稳定且具有高度可见光响应性的 AgCuO/Cu2O 半导体材料,以开发一种用于宽范围 Hg2+ 检测的比色法和光电化学(PEC)双传感模式。AgCuO/Cu2O 具有 Hg2+ 增强的过氧化物酶活性。在溶液中,Hg2+ 的出现促进 AgCuO/Cu2O 催化更多的 3,3′,5,5′-四甲基联苯胺(TMB)氧化,加深 TMB 溶液的颜色并增加光吸收,从而实现对 Hg2+ 的比色检测。其线性响应范围为 1 nmol-L-1 至 10 μmol-L-1,检测限为 3.5 nmol-L-1。在电极表面,Hg2+ 的出现促进 AgCuO/Cu2O 将更多的 4-chloro-1-naphthol (4-CN) 转化为不溶性沉淀物 benzo-4-chlorohexadienone (4-CD),从而抑制了 PEC 信号,实现了对 Hg2+ 的 PEC 检测,线性响应范围为 10 pmol-L-1 至 10 μmol-L-1,检测限为 8.7 pmol-L-1。Hg2+ 对 AgCuO/Cu2O 酶模拟活性的增强与 Ag-Hg 汞齐的原位形成密切相关。比色法和 PEC 传感模式相辅相成,大大拓宽了 Hg2+ 的检测范围,确保了检测结果的可靠性和准确性。这项工作为灵敏、选择性和准确测定血清样品中的 Hg2+ 铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AgCuO/Cu2O Nanozyme-Based Colorimetric and Photoelectrochemical Dual-Models Strategy for Sensing Hg2+ in Serum
A stable and highly visible-light responsive semiconductor material of AgCuO/Cu2O was prepared to develop a colorimetric and photoelectrochemical (PEC) dual-sensing mode for broad-range Hg2+ detection. The AgCuO/Cu2O was evidenced with Hg2+-enhanced peroxidase activity. In the solution, the appearance of Hg2+ promotes AgCuO/Cu2O to catalyze more 3, 3′, 5, 5′-tetramethylbenzidine (TMB) oxidization, deepening the color of the TMB solution and increasing the light absorption, thus realizing the colorimetric detection of Hg2+. The linear response range is 1 nmol·L-1 to 10 μmol·L-1, and the detection limit is 3.5 nmol·L-1. On the electrode surface, the emergence of Hg2+ facilitates AgCuO/Cu2O to convert more 4-chloro-1-naphthol (4-CN) into insoluble precipitates benzo-4-chlorohexadienone (4-CD), depressing the PEC signal and realizing the PEC detection of Hg2+ with a linear response range of 10 pmol·L-1 to 10 μmol·L-1 and a detection limit of 8.7 pmol·L-1. The enhancement of the enzyme-mimicking activity of AgCuO/Cu2O by Hg2+ is closely related to the in-situ formation of the Ag-Hg amalgam. The colorimetric and the PEC sensing modal complement each other, significantly broadening the detection range of Hg2+ and ensuring the reliability and accuracy of the results. The work paves the way for sensitive, selective, and accurate determination of Hg2+ in serum samples.
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