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      Characterization Techniques for Emulsion-Based Antioxidant Carriers with Biomedical Applications

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          Antioxidant activity applying an improved ABTS radical cation decolorization assay

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            Use of a free radical method to evaluate antioxidant activity

            LWT - Food Science and Technology, 28(1), 25-30
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              The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay.

              A simple, automated test measuring the ferric reducing ability of plasma, the FRAP assay, is presented as a novel method for assessing "antioxidant power." Ferric to ferrous ion reduction at low pH causes a colored ferrous-tripyridyltriazine complex to form. FRAP values are obtained by comparing the absorbance change at 593 nm in test reaction mixtures with those containing ferrous ions in known concentration. Absorbance changes are linear over a wide concentration range with antioxidant mixtures, including plasma, and with solutions containing one antioxidant in purified form. There is no apparent interaction between antioxidants. Measured stoichiometric factors of Trolox, alpha-tocopherol, ascorbic acid, and uric acid are all 2.0; that of bilirubin is 4.0. Activity of albumin is very low. Within- and between-run CVs are <1.0 and <3.0%, respectively, at 100-1000 micromol/liter. FRAP values of fresh plasma of healthy Chinese adults: 612-1634 micromol/liter (mean, 1017; SD, 206; n = 141). The FRAP assay is inexpensive, reagents are simple to prepare, results are highly reproducible, and the procedure is straightforward and speedy. The FRAP assay offers a putative index of antioxidant, or reducing, potential of biological fluids within the technological reach of every laboratory and researcher interested in oxidative stress and its effects.
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                Book Chapter
                2020
                February 23 2021
                : 423-462
                10.1007/978-3-030-62052-3_12
                4a1ca0fe-1af7-4e01-9e65-6e752a9c198c
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