2014
DOI: 10.1684/abc.2014.0971
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Determination of the plasma global antioxidant capacity: a critical review

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Cited by 3 publications
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“…Several spectrophotometric methods have been developed to measure plasma or serum TAC, such as Oxygen Radical Absorbance Capacity (ORAC), Total Radical-trapping Antioxidant Parameter (TRAP), and 2,2 -Azinobis-(3-Ethylbenzothiazolin-6-Sulfonic Acid (ABTS) [27], which should be more precisely renamed plasma or serum non-enzymatic antioxidant capacity (NEAC) [28]. A major drawback of these assays is that uric acid, the major antioxidant in plasma, reacts strongly with the free radicals used, thus masking the effects of other antioxidants such as vitamins C and E [29,30]. Recently, Carrion-Garcia et al [28] also reported a strong and significant correlation (r = 0.67, p value 2.02 × 10 −19 ) between uric acid and TAC, as assessed by the reduction of ferric iron (Fe 3+ ) to ferrous iron (Fe 2+ ) by antioxidants present in plasma samples (Ferric Reducing Antioxidant Power (FRAP)).…”
Section: Introductionmentioning
confidence: 99%
“…Several spectrophotometric methods have been developed to measure plasma or serum TAC, such as Oxygen Radical Absorbance Capacity (ORAC), Total Radical-trapping Antioxidant Parameter (TRAP), and 2,2 -Azinobis-(3-Ethylbenzothiazolin-6-Sulfonic Acid (ABTS) [27], which should be more precisely renamed plasma or serum non-enzymatic antioxidant capacity (NEAC) [28]. A major drawback of these assays is that uric acid, the major antioxidant in plasma, reacts strongly with the free radicals used, thus masking the effects of other antioxidants such as vitamins C and E [29,30]. Recently, Carrion-Garcia et al [28] also reported a strong and significant correlation (r = 0.67, p value 2.02 × 10 −19 ) between uric acid and TAC, as assessed by the reduction of ferric iron (Fe 3+ ) to ferrous iron (Fe 2+ ) by antioxidants present in plasma samples (Ferric Reducing Antioxidant Power (FRAP)).…”
Section: Introductionmentioning
confidence: 99%
“…Using a rat model, Gerardi et al [ 22 ] evidenced that the antioxidant capacity of plasma as measured by DPPH and FRAP assays was increased after intake of pomace products in a dose-response effect. Nevertheless, the use of both assays to evidence in vivo antioxidant activity largely remains a matter of debate [ 23 ]. In a more accurate way, Curti et al [ 24 ] showed in a mouse model that oral administration of whole brown propolis extract containing galangin is followed by rapid absorption and metabolization of the latter, resulting in adaptations of the antioxidant enzymatic defense system.…”
Section: Introductionmentioning
confidence: 99%
“…The most popular test is the ORAC (oxygen radical antioxidant capacity) assay which evaluates how antioxidants present in biological samples can inhibit, or not, physiological free radical species produced in a test tube. A very strong limitation of such an approach is that the plasma antioxidant capacity is dependent on uric acid and total protein concentrations of more than 70% [8,9].…”
Section: Introductionmentioning
confidence: 99%