生物传感器
线性范围
化学发光
胶体金
纳米颗粒
电化学气体传感器
安培法
核化学
组合化学
微分脉冲伏安法
抗坏血酸
循环伏安法
电极
分析物
选择性
纳米传感器
作者
Yuxin Pu,Mao Zhou,Peijin Wang,Qian Wu,Tingting Liu,Mingxiao Zhang
标识
DOI:10.1016/j.jelechem.2020.114374
摘要
Abstract In this work, the FeyCo3-y [Co (CN)6]2 Prussian blue analogues (Fe-Co-Co PBAs) was first used as the regenerable co-reaction accelerator in luminol-O2 system to accelerate the electrochemiluminescence (ECL) reaction rate of luminol and the co-reactant of O2 for signal amplification. Remarkably, the ECL intensity of luminol functionalized AuNPs@Fe-Co-Co (luminol-AuNPs@Fe-Co-Co) nanocomposite first synthesized as an ECL probe via a green and simple method exhibited ~41-fold enhancement compared with luminol-AuNPs. Because the Fe-Co-Co PBAs with excellent reversible redox property could accelerate the reduction of dissolved O2 to generate plenty of reactive oxygen species (ROSs) for promoting luminol to emit a strong ECL signal. In addition, Fe-Co-Co PBAs acted as a satisfying nanocarrier to immobilize more luminol-AuNPs. Owing to the strong quenching effect of glutathione (GSH) on the ECL emission of luminol, the constructed ECL sensor for the quantitative analysis of GSH performed an excellent linearity from 1.0 nM to 1.0 mM with a low detection limit of 0.11 nM. Simultaneously, the proposed sensor applied for GSH determination in human serum samples with desirable results. This work introduced a robust co-reaction accelerator into luminol-O2 system to enhance the ECL intensity, further widening the application of luminol-centric ECL sensor in the bioanalysis field.
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