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Fenton reaction-triggered colorimetric detection of phenols in water samples using unmodified gold nanoparticles

机译:使用Fenton反应触发的比色法检测未改性金纳米颗粒中水样中的酚

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摘要

This work demonstrates a rapid and sensitive colorimetric detection of phenols by using single-stranded DNA (ssDNA)-regulated gold nanoparticles (AuNPs) as indicators. AuNPs can be stabilized in the presence of ssDNA through electrostatic repulsion, which prevents the salt-induced aggregation of AuNPs in solution. However, hydroxyl radicals (OH) generated by the Fenton reaction can cleave the ssDNA on the nanoparticle surface into mono- or oligonucleotide fragments, disrupting AuNPs stability. Phenolic compounds are known to be capable of being degraded or oxidized by OH produced by Fenton reaction. Thus, phenols can effectively scavenge OH to avoid ssDNA cleavage, protecting AuNPs from salt-induced aggregation. The ability of phenols to scavenge OH provides a quantitative basis for phenol sensing. In this study, catechol and hydroquinone were selected as analytes and detected using the proposed ssDNA-AuNPs colorimetric probe. The detection sensitivities of the colorimetric sensor are 0.2-7.0 μM for catechol and 2.7-19 μM for hydroquinone. The proposed bioassay eliminates tedious sample pre-treatment and offers favorable sensitivity and selectivity for targets in the presence of other investigated metal ions and organic molecules. The detection limits are 0.11 μM for catechol and 1.6 μM for hydroquinone, with relative standard deviations of 3.7% for catechol and 4.8% for hydroquinone. The recovery rate of catechol in real water samples ranges from 95% to 116%, confirming the application potential of the method to measure phenols in real samples.
机译:这项工作演示了通过使用单链DNA(ssDNA)调节的金纳米颗粒(AuNPs)作为指示剂对苯酚进行快速灵敏的比色检测。 AuNPs可以通过静电排斥作用在ssDNA存在的情况下稳定,这可以防止盐诱导溶液中AuNPs的聚集。然而,通过芬顿反应产生的羟基自由基(OH)会将纳米颗粒表面上的ssDNA裂解为单核苷酸或寡核苷酸片段,从而破坏了AuNPs的稳定性。已知酚类化合物能够被Fenton反应产生的OH降解或氧化。因此,酚可以有效清除OH以避免ssDNA裂解,从而保护AuNPs免受盐诱导的聚集。酚清除OH的能力为酚感测提供了定量基础。在这项研究中,选择儿茶酚和对苯二酚作为分析物,并使用拟议的ssDNA-AuNPs比色探针进行检测。比色传感器的检测灵敏度对儿茶酚为0.2-7.0μM,对苯二酚为2.7-19μM。所提出的生物测定消除了繁琐的样品预处理,并在存在其他已调查的金属离子和有机分子的情况下,为目标提供了有利的灵敏度和选择性。儿茶酚的检出限为0.11μM,对苯二酚的检出限为1.6μM,邻苯二酚的相对标准偏差为3.7%,对苯二酚的相对标准偏差为4.8%。实际水样中邻苯二酚的回收率在95%至116%之间,这证实了该方法在实际样品中测定酚的应用潜力。

著录项

  • 来源
    《Sensors and Actuators》 |2016年第3期|593-599|共7页
  • 作者单位

    State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing, 10084, China;

    State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing, 10084, China;

    State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing, 10084, China;

    State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing, 10084, China;

    State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing, 10084, China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Gold nanoparticles; Fenton reaction; Phenol; Colorimetric sensor;

    机译:金纳米粒子;芬顿反应苯酚;比色传感器;

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