Food & Function 2015-06-01

Antioxidant activity of alkyl hydroxytyrosyl ethers in unsaturated lipids.

Rosa Cert, Andrés Madrona, José Luis Espartero, M Carmen Pérez-Camino

Index: Food Funct. 6 , 1999-2007, (2015)

Full Text: HTML

Abstract

The antioxidant activity of ethyl and octyl hydroxytyrosyl ethers toward lipids was determined using the Rancimat and open cup methods at high temperatures and 50 °C, respectively. The effect of the unsaturation of the matrix was evaluated using sunflower, soya, and fish refined oils. The antioxidant activities of alkyl hydroxytyrosyl ethers (HTy ethers), hydroxytyrosyl esters, and free hydroxytyrosol are similar, and are much higher than that of α-tocopherol at the same millimolar concentration. The relationship between the induction period and the concentration of the HTy ethers is a sigmoidal curve; an accurate concentration of HTy ethers is necessary to achieve maximum activity, as it increases with the level of matrix unsaturation. The presence of tocopherols in commercial oils affects the antioxidant effect of HTy ethers. Thus, the addition of a low concentration of HTy ethers results in a positive effect, whereas the effect of the addition of high amounts of ethers is slightly less than that of the phenol alone. The addition of HTy ethers to commercial refined oils increases the stability of the oils and preserves tocopherols and polyunsaturated fatty acids from oxidation, enabling the oils to maintain their nutritional properties for longer periods of time.


Related Compounds

Related Articles:

Two successive one-pot reactions leading to the expeditious synthesis of (−)-centrolobine.

[Tetrahedron Lett. 45(35) , 6603-6605, (2004)]

More Articles...