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Chrzczanowicz, J., Gawron, A., Zwolinska, A., de Graft-Johnson, J., Krajewski, W., Krol, M., Markowski, J., Kostka, T. and Nowak, D. (2008) Simple Method for Determining Human Serum 2,2-Diphenyl-1-Picryl-Hydrazyl (DPPh) Radical Scavenging Activity—Possible Application in Clinical Studies on Dietary Antioxidants. Clinical Chemistry and Laboratory Medicine, 46, 342-334.
https://doi.org/10.1515/CCLM.2008.062

has been cited by the following article:

• TITLE: A Novel Assay for Measuring Total Antioxidant Capacity in Whole Blood and Other Biological Samples

  AUTHORS: Riccardo Ciuti, Gianfranco Liguri

  KEYWORDS: Total Antioxidant Capacity, Free Radicals, Total Antioxidant Status, Oxidative Stress, Intracellular TAC

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.10 No.2, February 20, 2017

  ABSTRACT: A new method for rapidly determining total antioxidant capacity (TAC) in a biological sample has been devised and evaluated. A surfactant present in the reagent causes the lysis of cells in the sample. Glutathione, ascorbic acid, protein thiols and other main reducing substances in the sample react with a specific redox chromogen (2,6-dichlorophenolindophenol) and produce a change in the color of the reagent, which is determined photometrically at 630 nm. This new method quantifies the overall capacity of the sample to reduce a redox chromogen and it requires the minimum volumes and time. The assay can be used on a wide variety of biological samples including whole blood, serum, plasma, tissue extracts and homogenates, food, wine, fruit juice and other beverages. Results are expressed in terms of mmol/L glutathione equivalents. TAC can be assayed manually, on automatic analyzers or micro-plate readers.