Behavior of phenolic antioxidants in a partitioned medium: Structure-activity relationship

Citation
Me. Cuvelier et al., Behavior of phenolic antioxidants in a partitioned medium: Structure-activity relationship, J AM OIL CH, 77(8), 2000, pp. 819-823
Citations number
15
Categorie Soggetti
Agricultural Chemistry
Journal title
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY
ISSN journal
0003021X → ACNP
Volume
77
Issue
8
Year of publication
2000
Pages
819 - 823
Database
ISI
SICI code
0003-021X(200008)77:8<819:BOPAIA>2.0.ZU;2-9
Abstract
The behavior of phenolic antioxidants is studied in a partitioned medium, c omposed of linoleic acid dispersed in an aqueous phase. Their efficiency is measured by the diene production during oxidation, induced by Fe (II)/asco rbic acid at 30 degrees C. With a linoleic acid/Fe2+ molar ratio of 10 and a Fe2+/ascorbic acid molar ratio of 23, a steady-state propagation rate is reached after 1 h for up to 15 h. The antioxidants cannot avoid the early d ienes (30-40% of total dienes), resulting from the inducing reactions; howe ver, they can stop all the dienes produced during propagation reactions by acting on ROO.. The inhibition values reveal a great difference between the antioxidants, depending on their structure (number of hydroxyl groups or c helating sites) and on their polarity, confirming the "polar paradox." Thus , a-tocopherol, butylated hydroxytoluene, butylated hydroxyanisole, and iso eugenol appear to be the best antioxidants, but rosmarinic and caffeic acid s, generally potent antioxidants, present a weak efficiency. Surprisingly, in such a metal-induced system, the chelator activity seems to play a minor role.