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Effects of pH and ferric ions on the antioxidant activity of olive polyphenols in oil‐in‐water emulsions
Author(s) -
PaivaMartins Fátima,
Gordon Michael H.
Publication year - 2002
Publication title -
journal of the american oil chemists' society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.512
H-Index - 117
eISSN - 1558-9331
pISSN - 0003-021X
DOI - 10.1007/s11746-002-0524-4
Subject(s) - hydroxytyrosol , chemistry , oleuropein , ferric , phenols , chloride , polyphenol , antioxidant , tyrosol , phenol , nuclear chemistry , organic chemistry
The effects of four phenolic compounds occurring in olives and virgin olive oil, namely, oleuropein, hydroxytyrosol, 3,4‐dihydroxyphenylethanol‐elenolic acid (3,4‐DHPEA‐EA) and 3,4‐dihydroxyphenylethanol‐elenolic acid dialdehyde (3,4‐DHPEA‐EDA), on the oxidative stability of stripped olive oil‐in‐water emulsions were studied at three pH values in the presence or absence of ferric chloride at 60°C. In the stability test, the addition of phenolic compounds in emulsions at pH 5.5 significantly extended the induction time of lipid oxidation, and the activities in decreasing order were 3,4‐DHPEA‐EA> 3,4‐DHPEA‐EDA>hydroxytyrosol>α‐tocopherol∼oleuropein ≫control. The effect of concentration, iron, and pH on the antioxidant activity of the phenolic compounds in stripped olive oil‐in‐water emulsions was analyzed by response surface methodology. Oleuropein and hydroxytyrosol enhanced the prooxidant effect of ferric chloride at pH 3.5 and pH 5.5 but not at pH 7.4. The 3,4‐DHPEA‐EDA reduced the prooxidant effect of ferric chloride at pH 5.5 and pH 7.4, but at pH 3.5 prooxidant effects were evident at higher phenol concentration. The 3,4‐DHPEA‐EA reduced the prooxidant effect of ferric ions at all pH values tested. Differences in activity of the phenols may be explained by consideration of their free radical scavenging activity and ferric reducing capacity.