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A novel label-free fluorescence assay for one-step sensitive detection of Hg2+ in environmental drinking water samples

机译:一种新颖的无标记荧光测定法用于一步法灵敏检测环境饮用水样品中的Hg2 +

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摘要

A novel label-free fluorescence assay for detection of Hg2+ was developed based on the Hg2+-binding single-stranded DNA (ssDNA) and SYBR Green I (SG I). Differences from other assays, the designed rich-thymine (T) ssDNA probe without fluorescent labelling can be rapidly formed a T-Hg2+-T complex and folded into a stable hairpin structure in the presence of Hg2+ in environmental drinking water samples by facilitating fluorescence increase through intercalating with SG I in one-step. In the assay, the fluorescence signal can be directly obtained without additional incubation within 1 min. The dynamic quantitative working ranges was 5–1000 nM, the determination coefficients were satisfied by optimization of the reaction conditions. The lowest detection limit of Hg2+ was 3 nM which is well below the standard of U.S. Environmental Protection Agency. This method was highly specific for detecting of Hg2+ without being affected by other possible interfering ions from different background compositions of water samples. The recoveries of Hg2+ spiked in these samples were 95.05–103.51%. The proposed method is more viable, low-costing and simple for operation in field detection than the other methods with great potentials, such as emergency disposal, environmental monitoring, surveillance and supporting of ecological risk assessment and management.
机译:基于结合Hg 2 + 的单链DNA(ssDNA)和SYBR Green I(SG),开发了一种新型的无标记荧光检测Hg 2 + 的方法。一世)。与其他测定法不同,设计的无荧光标记的富胸腺嘧啶(T)ssDNA探针可以快速形成T-Hg 2 + -T复合物,并在存在Hg的情况下折叠成稳定的发夹结构通过与SG I一步一步嵌入来促进荧光增加,从而在环境饮用水样品中 2 + 。在测定中,可以直接获得荧光信号,而无需在1分钟内再孵育。动态定量工作范围为5–1000 nM,通过优化反应条件满足了测定系数。 Hg 2 + 的最低检出限为3 nM,远低于美国环境保护局的标准。该方法对检测Hg 2 + 具有很高的特异性,而不受来自水样品不同背景成分的其他可能干扰离子的影响。这些样品中加标的Hg 2 + 的回收率为95.05–103.51%。与应急处置,环境监测,生态风险评估和管理支持等具有较大潜力的方法相比,该方法可行,成本低,现场检测操作简单。

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