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pubmed-article:1610886pubmed:abstractTextPsoralens and other furocoumarins currently used in PUVA photochemotherapy are shown to have, to a variable extent, the ability to hasten the rate of ultraviolet-induced photooxidation of alpha-tocopherol (alpha-T) in ethanol or ethanol-phosphate buffer (pH 6.8). The sensitizing effect varies significantly with the substrate concentration and the nature of the furocoumarin used, and is dependent on the presence of oxygen. Scavengers of singlet oxygen, e.g., sodium azide, markedly inhibit the psoralen-sensitized photooxidation of alpha-T, whereas superoxide dismutase exerts an opposite, accelerating effect on the reaction rate. Catalase has no significant influence on the kinetics of alpha-T decay. Analysis of the products formed by psoralen-sensitized photooxidation of alpha-T in ethanol-phosphate buffer showed the presence of alpha-tocopherolquinone, its 2,3-epoxide and two related compounds containing the 7-oxaspiro[4.5]dec-1-ene-3,6-dione ring system. The nature of these products, coupled with the results of the kinetic experiments, suggest that psoralens induce a type II, oxygen-dependent photodegradation of alpha-T primarily mediated by singlet oxygen.lld:pubmed
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pubmed-article:1610886pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1610886pubmed:year1992lld:pubmed
pubmed-article:1610886pubmed:articleTitlePhotodynamic degradation of vitamin E induced by psoralens.lld:pubmed
pubmed-article:1610886pubmed:affiliationDepartment of Organic and Biological Chemistry, University of Naples, Italy.lld:pubmed
pubmed-article:1610886pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1610886pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed