CuO Nanozymes as Multifunctional Signal Labels for Efficiently Quenching the Photocurrent of ZnO/Au/AgSbS2 Hybrids and Initiating a Strong Fluorescent Signal in a Dual-Mode Microfluidic Sensing Platform

A novel dual-mode microfluidic sensing platform based on CuO nanozymes as a photoelectrochemical (PEC)-fluorescent (FL) multifunctional signal label was developed for ultrasensitive neuron specific enolase (NSE) detection. Herein, ZnO/Au/AgSbS2 hybrids, possessing excellent PEC properties, were first exploited as a sensing matrix to provide a stable photocurrent. The controlled synthesis of photoactive ZnO nanoflowers (NFs) was successfully conducted using a microfluidic reactor in the scale of seconds. Furthermore, the photocurrent of ZnO NFs decorated by Au and AgSbS2 nanoparticles significantly improved, owing to the local surface plasma resonance effect of Au and matching band structure between ZnO and AgSbS2. A strategy of catalytic oxidation ascorbic acid (AA) by CuO nanozymes was proposed to quench the PEC signals and initiate FL signals. CuO nanoparticles growing on conductive carbon spheres (CuO@CSs) as secondary antibodies' labels could efficiently catalyze the oxidation of AA to achieve a PEC signal-off state. Then, the produced dehydroascorbic acid reacting with o-phenylenediamine opportunely generated a strong FL signal. Importantly, wide linear ranges of 0.0001-150 ng/mL for the PEC technique and 0.001-150 ng/mL for the FL method with a low detection limit of 0.028 and 0.25 pg/mL, respectively, could guarantee the sensitive detection of NSE.

Automated summary

A novel dual-mode microfluidic sensing platform based on CuO nanozymes as a photoelectrochemical (PEC)-fluorescent (FL) multifunctional signal label was developed for ultrasensitive neuron specific enolase (NSE) detection. The platform utilized ZnO/Au/AgSbS2 hybrids as a sensing matrix to provide a stable photocurrent, and the controlled synthesis of photoactive ZnO nanoflowers (NFs) was successfully conducted using a microfluidic reactor. CuO nanozymes were employed to catalytically oxidize ascorbic acid (AA) and quench the PEC signals, while initiating FL signals through reaction with o-phenylenediamine. The platform exhibited wide linear ranges and low detection limits for both PEC and FL techniques, enabling sensitive detection of NSE.