利用钴基dna结合金属插层器†进行病原体核酸检测的电化学信号放大

IF 4.1 Q2 CHEMISTRY, ANALYTICAL
Joshua Rainbow, Emily P. Judd-Cooper, Simon J. A. Pope, Niklaas J. Buurma and Pedro Estrela
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引用次数: 0

摘要

本文报道了一种用于病原体核酸检测的高灵敏度、快速电化学生物传感器的研制。主要目的是提高DNA生物传感器对淡水和废水、食品工业和临床样品中常见的病原体核酸的检测灵敏度。这种增强的灵敏度是通过添加[Co(GA)2(aqphen)]Cl插入物来增加传感器表面/溶液界面的静电场来实现的。采用伏安法和阻抗检测技术表征了化合物的插层和氧化还原活性。此外,非法拉第阻抗法和伏安法被认为是电化学检测的合适技术。使用[Co(GA)2(aqphen)]Cl插入层导致使用DPV增加伏安信号输出,促进快速和敏感地检测目标DNA序列。值得注意的是,在没有[Fe(CN)6]3−/4−的情况下,[Co(GA)2(aqphen)]Cl允许使用非法拉第阻抗进行检测。通过循环伏安法表征,揭示了双链DNA (dsDNA)插层化合物具有表面控制氧化还原机制和可逆电化学反应。当1 μM靶DNA与200 μM [Co(GA)2(aqphen)]Cl结合时,电流峰值增加2250%。这使得在缓冲液中检测具有代表性的大肠杆菌DNA的靶DNA序列的LOD为67.5 pM,比标准的无标记检测灵敏100倍,同时保持检测简单,低成本和快速反应。在DNA生物传感器中的类似化合物中使用[Co(GA)2(aqphen)]Cl为检测诸如大肠杆菌等水媒病原体提供了一种经济有效且敏感的方法。这种方法可以通过更可靠和快速地监测水源中的病原体,大大改善环境监测和污染控制。此外,它在食品工业和护理点临床环境中有很大的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrochemical signal amplification for pathogen nucleic acid detection utilizing a cobalt-based DNA-binding metallo-intercalator†

Electrochemical signal amplification for pathogen nucleic acid detection utilizing a cobalt-based DNA-binding metallo-intercalator†

This paper reports the development of a highly sensitive and rapid electrochemical biosensor for the detection of pathogen nucleic acids. The primary objective was to enhance the detection sensitivity of DNA biosensors for pathogen nucleic acids commonly found in fresh and wastewaters, the food industry, and clinical samples. This enhanced sensitivity was achieved through the addition of a [Co(GA)2(aqphen)]Cl intercalating complex to increase the electrostatic field at the sensor surface/solution interface. Voltammetric and impedance-based detection techniques were employed to characterize the intercalation and redox-active properties of the compound. Additionally, non-faradaic impedance and voltammetric methods were characterized as appropriate techniques for electrochemical detection. Implementing the [Co(GA)2(aqphen)]Cl intercalator led to increased voltammetric signal output using DPV, facilitating the rapid and sensitive detection of target DNA sequences. Notably, the [Co(GA)2(aqphen)]Cl permitted detection using non-faradaic impedance in the absence of [Fe(CN)6]3−/4−. Characterization by cyclic voltammetric measurements revealed a surface-controlled redox mechanism and reversible electrochemistry of the compound intercalated with double-stranded DNA (dsDNA). Upon binding of 1 μM target DNA and 200 μM [Co(GA)2(aqphen)]Cl, a 2250% current peak increase was achieved. This increase enabled the sensitive detection of a target DNA sequence representative of E. coli DNA in buffer with an LOD of 67.5 pM, 100-fold more sensitive than the standard unlabeled assay while maintaining assay simplicity, low cost, and quick response. The use of [Co(GA)2(aqphen)]Cl among similar compounds in DNA biosensors offers a cost-effective and sensitive method for detecting waterborne pathogens such as E. coli. This approach could significantly improve environmental monitoring and pollution control by enabling more reliable and rapid monitoring of pathogens in water sources. Additionally, it has the potential to be of great use within the food industry and in point-of-care clinical settings.

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