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Mechanisms and Biomarkers (WG 4) page 26<br />

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usual antioxidant capacity assays are FRAP, TEAC and TRAP assays where the oxidants used<br />

are not necessarily prooxidants. Trolox equivalent antioxidant capacity (TEAC) assay (Miller<br />

et al., 1993) is based on the inhibition of the absorbance of the quite stable radical cation<br />

ABTS° + of ABTS with ferrylmyoglobin radical species generated by the activation of<br />

metmyoglobin with hydrogen peroxide. The assay measures the ability of antioxidants of<br />

given samples to reduce ABTS radical and compared with a reference, i.e. the Trolox, an<br />

hydrosoluble form of α-tocopherol. Ferric reducing ability of plasma (FRAP) assay (Benzie<br />

and Strain, 1996) measures the ability of biological samples to reduce the ferrictripyridyltriazine<br />

(Fe 3+ -TPZ) into Fe 2+ -TPZ reflecting the ability of the antioxidants within the<br />

sample to reduce the reactive species. This method is not suitable for glutathione<br />

determination and was weakly correlated with ORAC assay.<br />

Total Radical-Trapping Antioxidant Parameter (TRAP) is a fluorimetric assay (Ghiselli et al.,<br />

1995) that monitors the rate of peroxidation induced by thermal decomposition of 2,2diazobis-(2-amidinopropane)dihydrochloride<br />

through the loss of fluorescence of the protein<br />

R-phycoerythrin. Also in this assay the lag phase induced by plasma antioxidants is compared<br />

with that induced by Trolox.

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