4.7 Article

An on-off-on electrochemiluminescence aptasensor based on a self-enhanced luminophore for ochratoxin A detection

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 415, Issue 23, Pages 5833-5844

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-023-04864-8

Keywords

Electrochemiluminescence; Aptasensor; Self-enhanced luminophore; Ochratoxin A

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This study developed a highly selective and sensitive on-off-on electrochemiluminescence (ECL) aptasensor for the detection of ochratoxin A (OTA) using a self-enhanced luminophore. The aptasensor demonstrated good sensitivity, stability, and reproducibility, with a linear detection range of 0.1-320 ng/mL and a detection limit of 0.03 ng/mL. It provided a common analytical tool for the detection of mycotoxins and other small molecules.
A highly selective and sensitive on-off-on electrochemiluminescence (ECL) aptasensor based on a self-enhanced luminophore was developed for the detection of ochratoxin A (OTA). Specifically, polyethyleneimine functionalized multi-walled carbon nanotubes decorated with gold nanoparticles (AuNPs-PEI-MWCNTs) were used as the electrode matrix to accelerate electron transfer and provide a favorable microenvironment for self-enhanced luminophore loading and ECL signal enhancement. In addition, black phosphorus quantum dots (BPQDs) were used as co-reactants of the ECL reagent tris (2,2 & PRIME;-bipyridyl) ruthenium(II) (Ru(bpy)(3)(2+)) in ECL experiments, and the reaction mechanism was investigated. The self-enhanced luminophore Ru@SiO2-BPQDs was obtained by encapsulating Ru(bpy)(3)(2+) in silica (SiO2) nanoparticles and then combining it with BPQDs through electrostatic interaction. In conventional ECL systems, the emitter and its co-reactants reacted via the inter-nanoparticle pathway, leading to long distance electron transfer. However, the electron transfer distance in the self-enhanced luminophore was significantly shortened due to the intra-nanoparticle electron transfer pathway because BPQDs and oxidized Ru(bpy)(3)(2+) were bound within one nanoparticle, thereby improving ECL efficiency to achieve the first switch-on state. Then, the luminophore was quenched using ferrocenes (Fc) modified on an aptamer to achieve the switch-off state. Finally, OTA was specifically identified by the adapter, causing Fc to be released from the sensor interface, restoring the ECL intensity to achieve the second switch-on state. Under optimal conditions, the aptasensor exhibited good sensitivity, stability, and reproducibility, with a linear detection range from 0.1 to 320 ng/mL and a detection limit of 0.03 ng/mL. The novel ECL aptasensor provided a common analytical tool for the detection of mycotoxins and other small molecules.

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