{"title":"Natural Antioxidant Activity Evaluation Using Electrochemically Generated Superoxide Radical Anion: The SRAGE Assay.","authors":"Fatah Keffous, Abdallah Habab, Mohamed Abbaci, Abdelkrim Cheriti","doi":"10.1007/s12013-026-02130-z","DOIUrl":null,"url":null,"abstract":"<p><p>The antioxidant concentration and the redox potential of the oxidizing system employed in antioxidant assays are critical parameters governing the classification of antioxidant reducing power. In this study, we introduce the Superoxide Radical Anion Generated Electrochemically (SRAGE) assay, a novel electrochemical method for evaluating the antioxidant activity of natural compounds. Superoxide is the primary reactive oxygen species generated during the one-electron reduction of molecular oxygen in mitochondria, making it a biologically relevant probe for antioxidant evaluation and a distinct advantage over conventional 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) discoloration methods.In the SRAGE assay, [Formula: see text]is generated in situ by electrochemical reduction and subsequently scavenged by natural antioxidants, including rutin, ascorbic acid, quercetin, and gallic acid. The controlled generation of superoxide was achieved using cyclic voltammetry and was validated experimentally. At a concentration of 1mmol L- 1, the tested antioxidants exhibited inhibitory activities of 44.30 ± 1.31%, 52.01 ± 0.95%, 78.73 ± 2.02%, and 100.0 ± 0.12%, respectively. The ranking of antioxidant reducing power obtained from the SRAGE assay is in close agreement with that derived from the DPPH method. The proposed SRAGE assay offers a versatile electrochemical platform for evaluating the antioxidant activity of pure compounds and complex systems, including synthetic formulations, biological extracts, pharmaceutical products, and food additives.</p>","PeriodicalId":510,"journal":{"name":"Cell Biochemistry and Biophysics","volume":" ","pages":"4409-4421"},"PeriodicalIF":3.0000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biochemistry and Biophysics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12013-026-02130-z","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/12 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The antioxidant concentration and the redox potential of the oxidizing system employed in antioxidant assays are critical parameters governing the classification of antioxidant reducing power. In this study, we introduce the Superoxide Radical Anion Generated Electrochemically (SRAGE) assay, a novel electrochemical method for evaluating the antioxidant activity of natural compounds. Superoxide is the primary reactive oxygen species generated during the one-electron reduction of molecular oxygen in mitochondria, making it a biologically relevant probe for antioxidant evaluation and a distinct advantage over conventional 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) discoloration methods.In the SRAGE assay, [Formula: see text]is generated in situ by electrochemical reduction and subsequently scavenged by natural antioxidants, including rutin, ascorbic acid, quercetin, and gallic acid. The controlled generation of superoxide was achieved using cyclic voltammetry and was validated experimentally. At a concentration of 1mmol L- 1, the tested antioxidants exhibited inhibitory activities of 44.30 ± 1.31%, 52.01 ± 0.95%, 78.73 ± 2.02%, and 100.0 ± 0.12%, respectively. The ranking of antioxidant reducing power obtained from the SRAGE assay is in close agreement with that derived from the DPPH method. The proposed SRAGE assay offers a versatile electrochemical platform for evaluating the antioxidant activity of pure compounds and complex systems, including synthetic formulations, biological extracts, pharmaceutical products, and food additives.
期刊介绍:
Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems
The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized.
Examples of subject areas that CBB publishes are:
· biochemical and biophysical aspects of cell structure and function;
· interactions of cells and their molecular/macromolecular constituents;
· innovative developments in genetic and biomolecular engineering;
· computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies;
· photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design
For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.