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DNA-mediated assembly of carbon nanotubes for enhancing electrochemiluminescence and its application

机译:DNA介导的碳纳米管组装增强电化学发光及其应用

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Graphical abstractDisplay OmittedHighlightsLabel-free ECL DNA sensing strategy.Target dependent assembly of CNTs for ECL enhancement.Catalyzing electrochemical oxidation of TPrA to enhance ECL intensity.AbstractDNA adsorption and recognition are selective for carbon nanotubes (CNTs). In this work, we reported a novel method for control of electrochemiluminescence (ECL) enhancement through selective assembly of CNTs with DNA on indium tin oxide (ITO) electrode. The successful assembly of CNTs with well-preserved electrochemical conductivity was confirmed by scanning electron microscope and electrochemical impedance spectroscopy measurements. In comparison with the bare ITO electrode, the presence of CNTs catalyzes electrochemical reaction of an ECL coreactant, tri-n-propylamine, present in the solution, producing significantly enhanced ECL signal and ensuring substantial signal amplification. It is demonstrated that the efficiency of ECL enhancement is inversely correlated with the DNA recognition reaction, offering a promising ECL sensing platform for label-free and universal bioassay. The proposed strategy definitely differs from those works previously reported the introduction of CNTs for ECL enhancement, allowing the rise of ECL enhancement to be designed based on a biological recognition process. Just instead of the capture probe sequences, it is confirmed that the assembly of DNA with CNTs enables quantitative analysis of the different types of targets, including nucleic acid, Hg2+and thrombin.
机译: 图形摘要 省略显示 重点 无标签ECL DNA感应策略。 依赖目标的CNT组装以增强ECL。 催化TPrA的电化学氧化以增强ECL强度。 摘要 DNA吸附和识别对碳具有选择性纳米管(CNT)。在这项工作中,我们报告了一种通过在铟锡氧化物(ITO)电极上用DNA选择性组装CNTs来控制电化学发光(ECL)增强的新方法。通过扫描电子显微镜和电化学阻抗谱测量证实了具有良好保存的电化学电导率的CNT的成功组装。与裸露的ITO电极相比,碳纳米管的存在催化了溶液中存在的ECL共活化剂三 n -丙胺的电化学反应,产生了显着增强的ECL信号并确保了信号放大。结果表明,ECL增强的效率与DNA识别反应成反比,为无标记和通用生物测定提供了有希望的ECL传感平台。所提出的策略与先前报道的用于增强ECL的CNTs引入的工作完全不同,从而可以基于生物识别过程来设计ECL增强的兴起。只是代替了捕获探针序列,已确认DNA与CNT的组装可以定量分析不同类型的靶标,包括核酸Hg 2 + 和凝血酶。

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