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Electrochemical Detection of Ultratrace Lead Ion through Attaching and Detaching DNA Aptamer from Electrochemically Reduced Graphene Oxide Electrode

机译:通过电化学还原氧化石墨烯电极上的DNA适配子的分离和电化学检测超痕量铅离子

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摘要

This paper describes a simple strategy for the ultratrace level detection of Pb2+ ion based on G-quadruplex DNA and an electrochemically reduced graphene oxide (ERGO) electrode. First, ERGO was formed on a glassy carbon electrode (GCE) by the reduction of graphene oxide (GO) using cyclic voltammetry. Subsequently, a methylene blue (MB)-tagged, guanine-rich DNA aptamer (Apt) was attached to the surface of ERGO via π-π interaction, leading to the Apt-modified ERGO electrode. The presence of Pb2+ could generate the folding of Apt to a G-quadruplex structure. The formation of G-quadruplex resulted in detaching the Apt from the ERGO/GCE, leading to a change in redox current of the MB tag. Electrochemical measurements showed the proposed sensor had an exceptional sensitivity for Pb2+ with a linear range from 10−15 to 10−9 M and a detection limit of 0.51 fM. The sensor also exhibited high selectivity for Pb2+, as well as many other advantages, such as stability, reproducibility, regeneration, as well as simple fabrication and operation processes.
机译:本文介绍了一种基于G-四链体DNA和电化学还原氧化石墨烯(ERGO)电极的Pb 2 + 离子超痕量检测的简单策略。首先,通过使用循环伏安法还原氧化石墨烯(GO),在玻璃碳电极(GCE)上形成ERGO。随后,通过π-π相互作用将亚甲基蓝(MB)标记的富含鸟嘌呤的DNA适体(Apt)连接到ERGO的表面,从而形成Apt修饰的ERGO电极。 Pb 2 + 的存在可以使Apt折叠成G-四链体结构。 G-四链体的形成导致Apt与ERGO / GCE脱离,导致MB标签的氧化还原电流发生变化。电化学测量表明,该传感器对Pb 2 + 具有极高的灵敏度,线性范围为10 −15 至10 -9 M,并且检测极限为0.51 fM。该传感器还显示出对Pb 2 + 的高选择性,以及许多其他优点,例如稳定性,可重复性,再生以及简单的制造和操作过程。

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