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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Fluorometric determination of mercury(II) using positively charged gold nanoparticles, DNA-templated silver nanoclusters, T-Hg(II)-T interaction and exonuclease assisted signal amplification
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Fluorometric determination of mercury(II) using positively charged gold nanoparticles, DNA-templated silver nanoclusters, T-Hg(II)-T interaction and exonuclease assisted signal amplification

机译:荧光测定汞(II)使用带正电荷的金纳米颗粒,DNA模板银纳米蛋白,T-HG(II)-T相互作用和外切核酸酶辅助信号放大

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摘要

The authors describe a method for detection of Hg2+ by using positively charged gold nanoparticles ((+)AuNPs) as a quencher of the fluorescence of DNA-capped silver nanoclusters (DNA-AgNCs) which are negatively charged. In the presence of Hg2+, a DNA duplex is formed through T-Hg2+-T coordination chemistry. The duplex can be digested by exonuclease III to form smaller DNA fragments. This leads to the release of the AgNCs and the recovery of fluorescence, best measured at excitation/emission wavelengths of 460/530nm. The (+)AuNPs and Hg2+ are also released and can be reused for target recycling signal amplification. Based on these findings, a method is worked out for the determination of Hg2+ that works in the 5.0 pM to 10nM concentration range and has a detection limit as low as 2.3 pM. It is highly selective because of the highly specific formation of T-Hg2+-T bonds.
机译:作者描述了一种通过使用带正电荷的金纳米颗粒((+)AUNP)作为用于带负电荷的DNA封端的银纳米团簇(DNA-AGNC)的荧光的猝灭剂来检测HG2 +的方法。 在HG2 +存在下,通过T-HG2 + -T配位化学形成DNA双链体。 可以通过外切核酸酶III消化双链体以形成较小的DNA片段。 这导致AGNC的释放和荧光的恢复,在激发/发射波长为460 / 530nm的激发/发射波长下。 (+)AUNP和HG2 +也被释放,并且可以重复使用用于目标再循环信号放大。 基于这些发现,研究了一种方法,用于测定5.0pm至10nm浓度范围内的Hg2 +,并且具有低至2.3μm的检测限。 由于T-HG2 + -T键的高度特异性,它具有高度选择性。

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