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Coreactant Enhanced Anodic Electrochemiluminescence of CdTe Quantum Dots at Low Potential for Sensitive Biosensing Amplified by Enzymatic Cycle

机译:低灵敏度的CdTe量子点的共反应物增强的阳极电化学发光,通过酶促循环放大敏感的生物传感。

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This work used sulfite as a coreactant to enhance the anodic electrochemiluminescence (ECL) of mercaptopropionic acid modified CdTe quantum dots (QDs). This strategy proposed the first coreactant anodic ECL of QDs and led to a sensitive ECL emission of QDs in aqueous solution at relatively low potential. In the presence of dissolved oxygen, the stable ECL emission resulted from the excited QDs. Thus, an ECL detection method was proposed at +0.90 V (vs Ag/AgCl) based on the quenching of excited QDs by the analyte. Using tyrosine as a model compound, whose electrooxidized product could quench the excited QDs and thus the ECL emission, an analytical method for detection of tyrosine in a wide concentration range was developed. Furthermore, by combining an enzymatic cycle of trace tyrosinase to produce the oxidized product with an energy-transfer process, an extremely sensitive method for ECL detection of tyrosine with a subpicomolar limit of detection was developed. The sulfite-enhanced anodic ECL emission provided an alternative for traditional ECL light emitters and a new methodology for extremely sensitive ECL detection of mono- and dihydroxybenzenes at relatively low anodic potential. This strategy could be easily realized and opened new avenues for the applications of QDs in ECL biosensing.
机译:这项工作使用亚硫酸盐作为共反应剂来增强巯基丙酸修饰的CdTe量子点(QDs)的阳极电化学发光(ECL)。该策略提出了QD的第一个共反应剂阳极ECL,并导致在相对低电势下水溶液中QD的灵敏ECL发射。在存在溶解氧的情况下,稳定的ECL排放是由激发的QD引起的。因此,基于被分析物对激发的QD的猝灭,提出了一种在+0.90 V(vs Ag / AgCl)下的ECL检测方法。以酪氨酸为模型化合物,其电氧化产物可以猝灭激发的QD,从而消除ECL,因此开发了一种在宽浓度范围内检测酪氨酸的分析方法。此外,通过结合微量的酪氨酸酶的酶促循环以产生具有能量转移过程的氧化产物,开发了一种极灵敏的ECL检测酪氨酸的方法,其检测极限为亚皮摩尔。亚硫酸盐增强的阳极ECL发射为传统ECL发光器提供了一种替代方法,并且为在相对较低的阳极电势下对单和二羟基苯进行超灵敏ECL检测提供了一种新方法。这种策略很容易实现,并为QD在ECL生物传感中的应用开辟了新途径。

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