Inhibition of oxidation of methyl linoleate in solution by vitamin E and vitamin C.

E Niki, T Saito, A Kawakami, Y Kamiya - Journal of Biological Chemistry, 1984 - Elsevier
E Niki, T Saito, A Kawakami, Y Kamiya
Journal of Biological Chemistry, 1984Elsevier
The oxidation of methyl linoleate in solution initiated with azo compounds has been studied
in the absence and presence of vitamin E and vitamin C. Both vitamin E and vitamin C acted
as a chain-breaking antioxidant and they suppressed the oxidation and produced an
induction period. The inhibition rate constant for the scavenging of peroxy radical was
calculated at 37 degrees C as kinh= 5.1 X 10 (5) M-1 s-1 and 7.5 X 10 (4) M-1 s-1 for vitamin
E and vitamin C, respectively. It was suggested that each vitamin E could trap two peroxy …
The oxidation of methyl linoleate in solution initiated with azo compounds has been studied in the absence and presence of vitamin E and vitamin C. Both vitamin E and vitamin C acted as a chain-breaking antioxidant and they suppressed the oxidation and produced an induction period. The inhibition rate constant for the scavenging of peroxy radical was calculated at 37 degrees C as kinh = 5.1 X 10(5) M-1 s-1 and 7.5 X 10(4) M-1 s-1 for vitamin E and vitamin C, respectively. It was suggested that each vitamin E could trap two peroxy radicals, whereas vitamin C could trap only one peroxy radical under the reaction conditions employed in this study. When both vitamin E and vitamin C were present, the oxidation was suppressed quite efficiently and the apparent inhibition rate constant was obtained as kinh = 4.0 X 10(5) M-1 s-1. Furthermore, vitamin E remained almost unchanged and only vitamin C was consumed at the initial stage and vitamin E was consumed after vitamin C was exhausted. It was concluded that vitamin E trapped the peroxy radical and the resulting alpha-chromanoxy radical reacted with vitamin C to regenerate vitamin E.
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