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Updated: Jun 17, 2026

A Rapid and Specific Microplate Assay for the Determination of Intra- and Extracellular Ascorbate in Cultured Cells
Published on: April 11, 2014
A CoFe2O4 nanozyme mediated chemiluminescence imaging-colorimetric dual-mode sensor for monitoring ascorbic acid
Ye Zhang1, Maoying Peng1, Caiqiao Qin1
1School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P.R. China. zjyang@yzu.edu.cn.
Abstract:
Ascorbic acid (AA) participates in redox reactions in living organisms and scavenges free radicals to protect cells from oxidative damage. However, the conventional sensors for AA mainly rely on single-mode detection with insufficient accuracy. In this study, a CoFe2O4 nanozyme-mediated chemiluminescence (CL) imaging-colorimetric dual-mode sensor was proposed to monitor AA. CoFe PBA was utilized as a precursor to synthesize CoFe2O4 nanozymes through calcination, which shows high peroxidase-like activity. AA can efficiently scavenge ˙OH generated during CoFe2O4 nanozyme-catalyzed decomposition of H2O2. Due to the inhibitory effect of AA on the CoFe2O4 nanozyme-based catalytic system, the CL imaging-colorimetric dual-mode sensor was constructed to achieve rapid, accurate, and quantitative detection of AA. Experimental results demonstrate that as the AA concentration increases, the CL imaging intensity of the CoFe2O4-luminol-H2O2 system decreases, and the chromogenic reaction of the CoFe2O4-TMB-H2O2 system is significantly restrained (the blue coloration gradually fades). The detection ranges of AA are 20-200 μM (colorimetric) and 40-160 μM (CL imaging) with the detection limits of 18 μM and 25 μM, respectively. The developed dual-mode sensor features simple operation and a rapid signal response, and offers a promising approach for accurate determination of AA.
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