Cai Bin, Ren Tingyan, Yu Xiaowei, Lv Wendong, Liang Yong
Ministry of Ecology and Environment, South China Institute of Environmental Science, Guangzhou, 510655, China.
Institute of Resources Utilization and Rare Earth Development, Guangdong Academy of Sciences, Guangzhou, 510650, China.
Mikrochim Acta. 2024 Jan 3;191(1):74. doi: 10.1007/s00604-023-06142-x.
A universal strategy for a rapid colorimetric method for Hg in an aqueous solution is described. The specific binding of Hg (thymine-Hg-thymine) with thiolated DNA-functionalized gold nanoparticles (AuNPs) via Au-S bonds increases the spatial hindrance of the AuNP surface, resulting in a weakened catalytic ability of AuNPs to catalyze the reaction between p-nitrophenol and NaBH. Therefore, the color change time (CCT) of the solution from yellow to colorless becomes longer. Based on the kinetic curve of absorbance over time measured by a UV spectrometer, the level of Hg in aqueous solutions can be easily quantified. A linear relationship between CCT and Hg concentration was obtained in the 10-600-nM range with a detection limit of 0.20 nM, which is much lower than the limit value (10 nM) defined by the US Environmental Protection Agency for Hg in drinking water. The excellent sensitivity comes from CCT as the signal output of the probe, rather than the absorbance or wavelength change used in traditional colorimetric probes as the signal output.
本文描述了一种用于水溶液中汞的快速比色法的通用策略。汞(胸腺嘧啶-汞-胸腺嘧啶)通过金-硫键与硫醇化DNA功能化金纳米粒子(AuNPs)的特异性结合增加了AuNP表面的空间位阻,导致AuNPs催化对硝基苯酚与硼氢化钠之间反应的能力减弱。因此,溶液从黄色变为无色的颜色变化时间(CCT)变长。基于紫外光谱仪测量的吸光度随时间的动力学曲线,可以轻松定量水溶液中的汞含量。在10 - 600 nM范围内获得了CCT与汞浓度之间的线性关系,检测限为0.20 nM,远低于美国环境保护局规定的饮用水中汞的限值(10 nM)。优异的灵敏度来自于作为探针信号输出的CCT,而不是传统比色探针中使用的吸光度或波长变化作为信号输出。