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Spectrophotometric Determination of Trace Hg~(2+) with hsDNA-modified Nanosilver Probe

机译:具有HSDNA改性的纳米单向探针的分光光度法测定痕量HG〜(2+)

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Herring sperm DNA (hsDNA) was used to modify 5 nm nanosilver to obtain a hsDNA-nanosilver probe (Ag-hsDNA) for (Hg)~(2+). In the presence of (Hg)~(2+), it combined with hsDNA to produce Hg~(2+)-hsDNA complexes and to release nanosilver particles, based on formation of stable T-(Hg)~(2+)-T mismatches. Nanosilver particles aggregated to form larger nanosilver clusters and led the absorption at 412 nm decreased in the pH 6.5 Na_2HPO_4-NaH_2PO_4 buffer solution and 0.05 mol/L NaCl medium. The decreased absorption (△A_(412 nm)) is linear to Hg~(2+) concentration in the range of 1.36-10.86μg/L Hg~(2+), with regress equation of △A=0.0987C_(Hg)~(2+) +0.0624, correlation coefficient of 0.9890, and detection limit of 0.30μg/L (Hg)~(2+). The assay was applied to the analysis of (Hg)~(2+) in wastewater with satisfactory results.
机译:使用鲱鱼精子DNA(HSDNA)来改变5nM纳米液,得到(Hg)〜(2+)的HSDNA-Nanosilver探针(Ag-HsDNA)。在(Hg)〜(2+)的存在下,它与HSDNA合并以产生Hg〜(2 +) - HsDNA复合物并根据稳定的T-(Hg)〜(2 +)的形成释放纳米ilmer颗粒 - 不匹配。纳米玻璃颗粒聚集形成较大的纳米玻璃簇,并在412nm处的吸收在pH 6.5 Na_2HPO_4-NaH_2PO_4缓冲溶液和0.05mol / L NaCl培养基中降低。减少的吸收(△A_(412nm))是线性至Hg〜(2+)浓度,范围为1.36-10.86μg/ l hg〜(2+),具有χ= 0.0987c_(hg)的返回方程〜(2+)+0.0624,相关系数为0.9890,检测限为0.30μg/ L(Hg)〜(2+)。将测定法应用于废水中(Hg)〜(2+)的分析,具有令人满意的结果。

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