College of Food Science and Engineering, Northwest A&F University, Yangling, 712100, Shaanxi, China.
Qinghai Key Laboratory of Qinghai-Tibet Plateau Biological Resources, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, 810008, Qinghai, China.
Biosens Bioelectron. 2022 Nov 1;215:114519. doi: 10.1016/j.bios.2022.114519. Epub 2022 Jun 28.
The nanozyme-based colorimetric strategy for heavy metal detection has broad application prospects nowadays. However, the inefficient recognition capabilities of nanozyme sensors for targets hinder its further application. Herein, the authors synthesize bare nickel selenide (NiSe) via a one-step hydrothermal reaction, in which the Se element possesses a strong binding ability with mercury (Hg). As expected, NiSe exhibits oxidase-like activity in the presence of Hg, that is, Hg can enhance the oxidase-like activity of NiSe. The enhanced mechanism is the accelerated electron transfer between NiSe-Hg and substrate caused by the formation of Hg-Se bonds. Besides, the oxidase-like activity of NiSe exhibits excellent selectivity, sensitivity and stability in response to Hg, which enables NiSe-Hg to efficiently oxidize colorless TMB to blue TMB even in harsh environments. Based on this, a dual-mode colorimetric sensor integrating solution reaction and test paper is developed for the detection of Hg. In the Hg concentration range of 10-700 nM, the colorimetric platform presents a liner response to Hg, which can reach a low LOD of 5.18 nM in solution reaction and 8.42 nM in the test paper. The proposed strategy can also be applied to real water samples with good recovery and excellent self-calibration capability.
基于纳米酶的比色策略在重金属检测方面具有广阔的应用前景。然而,纳米酶传感器对目标物的识别能力不足,限制了其进一步的应用。在此,作者通过一步水热反应合成了裸镍硒(NiSe),其中硒元素与汞(Hg)具有很强的结合能力。不出所料,NiSe 在存在 Hg 的情况下表现出类氧化酶活性,即 Hg 可以增强 NiSe 的类氧化酶活性。增强机制是由于 Hg-Se 键的形成,加速了 NiSe-Hg 和底物之间的电子转移。此外,NiSe 的类氧化酶活性对 Hg 表现出优异的选择性、灵敏度和稳定性,这使得 NiSe-Hg 能够在恶劣环境下高效地将无色 TMB 氧化为蓝色 TMB。基于此,开发了一种集成溶液反应和试纸的双通道比色传感器用于检测 Hg。在 10-700 nM 的 Hg 浓度范围内,比色平台对 Hg 呈现线性响应,在溶液反应中的检测限低至 5.18 nM,在试纸上的检测限低至 8.42 nM。该策略还可用于实际水样,具有良好的回收率和出色的自校准能力。