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Novel Dual-Potential Color-Resolved Luminophore Ru(bpy)32+-Doped CdSe QDs for Bipolar Electrode Electrochemiluminescence Biosensing

发光体 电化学发光 化学 兴奋剂 电极 生物传感器 纳米技术 分析化学(期刊) 无机化学 光电子学 发光 物理化学 色谱法 生物化学 物理 材料科学
作者
Hongkun Li,Qianqian Cai,Minghao Bai,Guifen Jie
出处
期刊:Analytical Chemistry [American Chemical Society]
标识
DOI:10.1021/acs.analchem.4c05678
摘要

The classical electrochemiluminescence (ECL) reagent Ru(bpy)32+ was first doped into CdSe QDs to prepare novel dual-potential color-resolved luminophore Ru-CdSe QDs. Ru-CdSe QDs emitted a strong red ECL signal at a positive potential with coreactant TPrA and a strong green ECL signal at a negative potential with coreactant K2S2O8. As a proof-of-concept application, this work introduced Ru-CdSe QDs into a dual-channel closed bipolar electrode (CBPE) system to construct an ECL biosensor for simultaneous detection of chloramphenicol (CAP) and kanamycin (KAN). Ru-CdSe QDs were dropped on BPE holes A and B for ECL emission. Cobalt single-atom catalysts (Co–N–C SACs) had superior electric double layer (EDL) performance and conductivity. It could greatly promote the electron transfer of the CBPE system and realize ECL signal amplification. Based on this characteristic, Co–N–C SACs were introduced into BPE hole C and driving electrode hole D, respectively, using the CAP and KAN split dual-aptamer sandwich strategy. During positive potential scanning, the polarity of BPE hole A was anode, and Ru-CdSe QDs emitted a red ECL signal. With the increase of CAP concentration, abundant Co–N–C SACs were introduced to the electrode surface. The positive potential ECL signal was increased for CAP detection. During negative potential scanning, the polarity of the BPE hole B was cathode, and Ru-CdSe QDs emitted a green ECL signal for KAN detection. Finally, a zero-background spatial-potential color-resolved CBPE–ECL biosensor was developed for dual-mode detection of CAP and KAN. This work explored a novel ECL luminophore to construct a CBPE–ECL sensor, which greatly facilitated the development of the ECL assay.
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