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基于 DNA 功能化金纳米粒子的测试条平台,用于现场检测汞(II)离子。

A test strip platform based on DNA-functionalized gold nanoparticles for on-site detection of mercury (II) ions.

机构信息

Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, PR China.

出版信息

Talanta. 2012 May 15;93:49-54. doi: 10.1016/j.talanta.2012.01.012. Epub 2012 Jan 11.

DOI:10.1016/j.talanta.2012.01.012
PMID:22483875
Abstract

A test strip, based on DNA-functionalized gold nanoparticles for Hg(2+) detection, has been developed, optimized and validated. The developed colorimetric mercury sensor system exhibited a highly sensitive and selective response to mercury. The measurement principle is based on thymine-Hg(2+)-thymine (T-Hg(2+)-T) coordination chemistry and streptavidin-biotin interaction. A biotin-labeled and thiolated DNA was immobilized on the gold nanoparticles (AuNPs) surface through a self-assembling method. Another thymine-rich DNA, which was introduced to form DNA duplexes on the AuNPs surface with thymine-Hg(2+)-thymine (T-Hg(2+)-T) coordination in the presence of Hg(2+), was immobilized on the nitrocellulose membrane as the test zone. When Hg(2+) ions were introduced into this system, they induced the two strands of DNA to intertwist by forming T-Hg(2+)-T bonds resulting in a red line at the test zone. The biotin-labeled and thiolated DNA-functionalized AuNPs could be captured by streptavidin which was immobilized on the nitrocellulose membrane as the control zone. Under optimized conditions, the detection limit for Hg(2+) was 3 nM, which is lower than the 10nM, maximum contaminant limit defined by the US Environmental Protection Agency (EPA) for drinking water. A parallel analysis of Hg(2+) in pool water samples using cold vapor atomic absorption spectrometry showed comparable results to those obtained from the strip test. Therefore, the results obtained in this study could be used as basic research for the development of Hg(2+) detection, and the method developed could be a potential on-site screening tool for the rapid detection of Hg(2+) in different water samples without special instrumentation. All experimental variables that influence the test strip response were optimized and reported.

摘要

已开发、优化和验证了一种基于 DNA 功能化金纳米粒子用于 Hg(2+)检测的测试条。所开发的比色汞传感器系统对汞表现出高度灵敏和选择性的响应。测量原理基于胸腺嘧啶-Hg(2+)-胸腺嘧啶 (T-Hg(2+)-T) 配位化学和链霉亲和素-生物素相互作用。通过自组装方法将生物素标记和硫醇化 DNA 固定在金纳米粒子 (AuNPs) 表面上。另一种富含胸腺嘧啶的 DNA 被引入,在存在 Hg(2+) 的情况下,在 AuNPs 表面上形成 DNA 双链,与胸腺嘧啶-Hg(2+)-胸腺嘧啶 (T-Hg(2+)-T) 配位,固定在硝酸纤维素膜上作为测试区。当 Hg(2+) 离子引入该系统时,它们通过形成 T-Hg(2+)-T 键诱导两条 DNA 链缠绕,导致测试区出现红线。固定在硝酸纤维素膜上作为对照区的链霉亲和素可以捕获生物素标记和硫醇化 DNA 功能化的 AuNPs。在优化条件下,Hg(2+) 的检测限为 3 nM,低于美国环境保护署 (EPA) 规定的饮用水中 10 nM 的最大污染物限量。使用冷蒸气原子吸收光谱法对池塘水样中的 Hg(2+) 进行平行分析,结果与条带测试获得的结果相当。因此,本研究获得的结果可用于 Hg(2+) 检测的基础研究,所开发的方法可作为一种潜在的现场筛选工具,用于快速检测不同水样中的 Hg(2+),而无需特殊仪器。报告了影响测试条响应的所有实验变量的优化结果。

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