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Updated: Aug 14, 2026

A Rapid and Specific Microplate Assay for the Determination of Intra- and Extracellular Ascorbate in Cultured Cells
Published on: April 11, 2014
Exploration and quantification of ascorbate affecting peroxidase-catalyzed chromogenic reactions with a
Yong-Sheng Li1, Yang Zhao, Qiao-Jing Li
1School of Chemical Engineering, Sichuan University, Chengdu 6100651, China. lysgxf2005@qq.com.
Abstract:
The use of a recirculating-flow catalysis detection system (RFCD) explored competition and the influence of ascorbic acid (AsA) in peroxidase (POD)-catalyzed reactions. The study identified that AsA is neither the inhibitor of POD nor could directly deplete H2O2; it directly reacts with chromogenic products to form colorless intermediates, which can react with H2O2 to again rapidly re-generate the chromogenic products. If using the reactions (trinder reactions or enzyme-linked reactions) to determine POD activity (EPOD), substrates or analytes, the interference of concomitant AsA should be removed and the conclusions have significance for oxidase/POD catalyzed reactions. In addition, the RFCD system was also used to simultaneously determine EPOD and AsA.

