G
Graham W. Burton
Researcher at National Research Council
Publications - 92
Citations - 9773
Graham W. Burton is an academic researcher from National Research Council. The author has contributed to research in topics: Vitamin E & Antioxidant. The author has an hindex of 39, co-authored 92 publications receiving 9519 citations. Previous affiliations of Graham W. Burton include Toronto General Hospital.
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Journal ArticleDOI
The relative contributions of vitamin E, urate, ascorbate and proteins to the total peroxyl radical-trapping antioxidant activity of human blood plasma.
TL;DR: The changes in concentrations of the plasma antioxidants during peroxyl radical attack show that the first line of defense is provided by the plasma sulfhydryl groups, even urate being spared during the initial stages of the reaction.
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Is vitamin E the only lipid-soluble, chain-breaking antioxidant in human blood plasma and erythrocyte membranes?
TL;DR: It is concluded that vitamin E, which is largely present as alpha-tocopherol, is the only significant lipid-soluble, chain-breaking type of antioxidant present in human blood.
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Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols
Graham W. Burton,Takahisa Doba,Eric J. Gabe,L. Hughes,Florence L. Lee,L. Prasad,Keith U. Ingold +6 more
TL;DR: On mesure les constantes de vitesse de l'elimination of l'hydrogene atomique par les radicaux peroxyles de lα-tocopherol and de 35 phenols structuralement apparentes.
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Vitamin E: Antioxidant Activity, Biokinetics, and Bioavailability
Graham W. Burton,Maret G. Traber +1 more
TL;DR: Pour mesurer l'absorption et le transport de la vitamine E, utilisation d'un isotope stable marque et analyse par chromatographie gazeuse et spectrometrie de masse.
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Quantitative measurement of the total, peroxyl radical-trapping antioxidant capability of human blood plasma by controlled peroxidation. The important contribution made by plasma proteins.
TL;DR: Evidence is presented to show that this previously unrecognized large reserve of antioxidant capacity is attributable to the plasma proteins.