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Visual and On-site Detection of Mercury(II) Ions on Lateral Flow Strips Using DNA-functionalized Gold Nanoparticles

机译:使用DNA功能化的金纳米粒子对侧流试纸上的汞(II)离子进行视觉和现场检测

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A test strip for detection of Hg~(2+) in aqueous solution based on the DNA-functionalized gold nanoparticles (DNA-AuNPs) was developed and evaluated. When Hg~(2+) ions were introduced, the biotinylated DNA_(2) hybridized with thiolated DNA_(1) functionalized on the AuNPs (DNA_(1)-AuNPs) to form mismatch complexes through thymine-Hg~(2+)-thymine (T-Hg~(2+)-T) coordination. The formed mismatch complexes and excess DNA_(1)-AuNPs could be captured on the test line formed by streptavidin and the control line formed by DNA_(3)-BSA, respectively. Two red lines appeared due to the accumulation of AuNPs, enabling visual detection of Hg~(2+) with a detection limit of about 6 nM. The assay results can be obtained within 5 min. The results show that the test strip has excellent sensitivity and selectivity for detection of Hg~(2+); thus it holds a great potential for rapid, on-site and real time detection of Hg~(2+).
机译:开发并评估了一种基于DNA功能化金纳米粒子(DNA-AuNPs)的水溶液中Hg〜(2+)检测试纸。当引入Hg〜(2+)离子时,生物素化的DNA_(2)与在AuNPs(DNA_(1)-AuNPs)上官能化的巯基化的DNA_(1)杂交,通过胸腺嘧啶-Hg〜(2 +)-形成错配复合物。胸腺嘧啶(T-Hg〜(2 +)-T)的配位。形成的错配复合物和过量的DNA_(1)-AuNPs可以分别捕获在链霉亲和素形成的测试线上和DNA_(3)-BSA形成的对照线上。由于AuNPs的积累,出现了两条红线,从而可以视觉检测Hg〜(2+),检测极限约为6 nM。测定结果可在5分钟内获得。结果表明,该试纸对Hg〜(2+)的检测具有很好的灵敏度和选择性。因此,它具有快速,现场和实时检测Hg〜(2+)的巨大潜力。

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