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Journal ArticleDOI

The peroxidizing effect of α-tocopherol on autoxidation of methyl linoleate in bulk phase.

Junji Terao, +1 more
- 01 Apr 1986 - 
- Vol. 21, Iss: 4, pp 255-260
TLDR
It is suggested that α-tocopherol at high concentrations influences the mechanism of autoxidation of edibleOil under storage conditions and a mechanism in which chromanoxy radical participates is proposed.
Abstract
In order to understand the effect of α-tocopherol on the autoxidation mechanism of edible oil under storage conditions, methyl linoleate was allowed to autoxidize at 50 C in bulk phase without any radical initiator. The reaction was monitored by determining the production of four isomeric hydroperoxides (13-cis,trans; 13-trans,trans; 9-cis,trans; 9-trans,trans) by high performance liquid chromatographic analysis after reduction. In the absence of α-tocopherol, the rate of autoxidation depended on the sample size, and the duration of the induction period was affected by the initial level of hydroperoxides. However, the distribution of c-t and t-t hydroperoxide isomers remained constant during the propagation period regardless of the sample size. The addition of α-tocopherol at 0.1 and 1.0% caused a linear increase in the amount of hydroperoxides and elevated the distribution of the c-t isomers. The rate of hydroperoxidation appeared to be governed by the initial concentration of α-tocopherol rather than the sample size or the initial hydroperoxide level. This peroxidizing effect of α-tocopherol was suppressed by the presence of ascorbyl palmitate. A mechanism in which chromanoxy radical participates is proposed for the effect of α-tocopherol on lipid autoxidation in bulk phase. It is therefore suggested that α-tocopherol at high concentrations influences the mechanism of autoxidation of edible oil.

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Citations
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Journal ArticleDOI

The chemistry and antioxidant properties of tocopherols and tocotrienols

TL;DR: Some possible reasons for the observed differences between the tocopherols (α-, β-, γ-, and δ-) in relation to their interactions with the important chemical species involved in lipid peroxidation, specifically trace metal ions, singlet oxygen, nitrogen oxides, and antioxidant synergists are highlighted.
Journal ArticleDOI

Mechanisms and Factors for Edible Oil Oxidation

TL;DR: In this article, the authors studied the role of chlorophyll as a photosensitizer for the formation of 1O2; however, carotenoids and tocopherols decrease the oxidation through 1O 2 quenching.
Journal ArticleDOI

Mechanisms of free radical oxidation of unsaturated lipids

TL;DR: The mechanisms of these primary reaction steps has been the focus of extensive research over the past fifty years, and the current level of understanding of these transformations is the subject of this review.
Journal ArticleDOI

Antioxidants in relation to lipid peroxidation

TL;DR: The role of antioxidants in lipid peroxidation is reviewed and the rate and mechanism of inhibition by water-soluble and lipid-Soluble, chain-breaking antioxidants have been discussed.
References
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Journal ArticleDOI

Direct observation of a free radical interaction between vitamin E and vitamin C

TL;DR: Direct observation of the interaction between vitamin E and vitamin C and the resulting vitamin E radical then reacting with vitamin C to regenerate vitamin E is reported, which is felt to be an important feature in the maintenance of vitamin E levels in tissues.
Journal ArticleDOI

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

TL;DR: It was concluded that vitamin E trapped the peroxy radical and the resulting alpha-chromanoxy radical reacted with vitamin C to regenerate vitamin E.
Journal ArticleDOI

Separation of lipid classes by chromatography on Florisil.

TL;DR: Preliminary experiments indicated that chromatography on Florisil gave good separations of lipid classes of naturally occurring lipids extracted from liver and blood.
Journal ArticleDOI

Autoxidation of methyl linoleate. Separation and analysis of isomeric mixtures of methyl linoleate hydroperoxides and methyl hydroxylinoleates

Henry W.-S. Chan, +1 more
- 01 Jan 1977 - 
TL;DR: The mixture of conjugated diene hydroperoxide isomers obtained from autoxidation of methyl linoleate was separated by high performance liquid chromatography (HPLC) and provides a rapid method for their analysis.
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