Radical scavenging ability of polyphenolic compounds towards DPPH free radical

Free radical scavenging activity of different polyphenolic compounds commonly present in wine has been evaluated using DPPH method. The experiments were performed with different amounts of phenols within the linear interval of response and with an excess of DPPH center dot in all cases. In these conditions, for most of the compounds tested, the reaction was biphasic. Total stoichiometry values n confirm the implication of more than one step in the process. Flavan-3-ol compounds showed the highest values, especially procyanidins B 1 (9.8) and B2 (9. 1). In this family, n values coincide with the number of hydroxyl groups available. EC50 and TEC50 parameters have been calculated. EC50 values are extremely diverse, being the procyanidins B I and B2 the most potent scavenging compounds and resveratrol the less one. TEC50 considers the rate of reaction towards the free radical. (+)-Catechin and (-)-epicatechin are the phenolic compounds that need more time to react. In contrast, caftaric and caffeic acids are the phenolic acids that react more rapidly. Antioxidant efficacy (AE) is a parameter that combines both factors. Compounds as kaempferol, with a high EC50 value, could be considered as an antioxidant with low relevance, but instead shows the highest AE value of the phenolic compounds tested, due to its fast rate of reaction, what is of great biological importance. (c) 2006 Elsevier B.V. All rights reserved.