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A simple and rapid resonance scattering spectral method for detection of trace Hg~(2+) using aptamer-nanogold as probe

机译:一种以适配子-纳米金为探针检测痕量Hg〜(2+)的简单快速共振散射光谱法

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摘要

Single-strand deoxyribonucleic acid (ssDNA) were used to modified nanogold particle to obtain a aptamer-nanogold probe (NGssDNA) for Hg(II). The probe is not aggregated in high concentration of NaCl. In the pH 7.0 Na_2HPO_4-NaH_2PO_4 buffer solution and in the presence of high concentration of NaCl, NGssDNA interact with Hg(II) to form stable double-strand T-Hg(II)-T mismatches and to release nanogold particles from the probe. The released nanogold particles aggregated to form bigger clusters which leaded the resonance scattering (RS) intensity at 540 nm enhanced linearly with the concentration of Hg~(2+) in the range of 0.39-1666.7 nM, with detection of 0.1 nM. This simple, rapid, and sensitive aptamer-nanogold RS assay was applied to determination of Hg~(2+) in wastewater, with satisfactory results.
机译:用单链脱氧核糖核酸(ssDNA)修饰纳米金颗粒,得到Hg(II)的适体-纳米金探针(NGssDNA)。探针未在高浓度的NaCl中聚集。在pH 7.0的Na_2HPO_4-NaH_2PO_4缓冲溶液中,在高浓度的NaCl存在下,NGssDNA与Hg(II)相互作用,形成稳定的双链T-Hg(II)-T错配,并从探针中释放出纳米金颗粒。释放出的纳米金粒子聚集形成更大的簇,导致在540 nm处的共振散射(RS)强度随Hg〜(2+)的浓度在0.39-1666.7 nM范围内线性增加,检测值为0.1 nM。该简单,快速,灵敏的适体-纳米金RS测定方法用于废水中Hg〜(2+)的测定,结果令人满意。

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