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首页> 外文期刊>Luminescence: The journal of biological and chemical luminescence >Resonance scattering spectral detection of ultratrace Hg(II) using herring sperm DNA modified nanogold probe as catalyst
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Resonance scattering spectral detection of ultratrace Hg(II) using herring sperm DNA modified nanogold probe as catalyst

机译:鲱鱼精DNA修饰的纳米金探针催化超痕量汞的共振散射光谱检测

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摘要

Herring sperm DNA (hsDNA) was used to modify 10 nm nanogold to obtain a resonance scattering (RS) probe (AuhsDNA) for detection of Hg~(2+). In the presence of salt, Hg~(2+) interacts with AuhsDNA to form stable Hg~(2+)-hsDNA complexes, and releases nanogold particles to form larger nanogold clusters that can be removed by membrane filtration. The excess AuhsDNA in the filtrate solution exhibits a catalytic effect on the reaction between hydroxylamine (NH_2OH) and Cu(II). The excess AuhsDNA decreased with the addition of Hg~(2+), which led the RS intensity at 602 nm to decrease. The decreased RS intensity (Δl_(602 nm)) had a linear response to Hg~(2+) concentration in the range of 0.4-400 nM, with a detection limit of 0.2 nM Hg~(2+). This RS method was applied for the detection of Hg~(2+) in water samples, with sensitivity, selectivity and simplicity.
机译:用鲱鱼精DNA(hsDNA)修饰10 nm纳米金,得到共振散射(RS)探针(AuhsDNA),用于检测Hg〜(2+)。在盐的存在下,Hg〜(2+)与AuhsDNA相互作用形成稳定的Hg〜(2 +)-hsDNA复合物,并释放出纳米金颗粒,形成较大的纳米金簇,可以通过膜过滤将其去除。滤液中过量的AuhsDNA对羟胺(NH_2OH)与Cu(II)之间的反应具有催化作用。过量的AuhsDNA随着Hg〜(2+)的添加而减少,导致602 nm处的RS强度降低。降低的RS强度(Δl_(602nm))对Hg〜(2+)的浓度具有线性响应,范围为0.4-400nM,检测极限为0.2nM Hg〜(2+)。该RS方法用于水样中Hg〜(2+)的检测,灵敏度高,选择性好,操作简便。

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