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    One-electron reduction potentials of dietary carotenoid radical cations in aqueous micellar environments.

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    Authors
    Burke, Marc
    Edge, Ruth
    Land, Edward J
    McGarvey, David J
    Truscott, T G
    Affiliation
    School of Chemistry and Physics, Keele University, UK.
    Issue Date
    2001-07-06
    
    Metadata
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    Abstract
    The one-electron reduction potentials of the radical cations of five dietary carotenoids (beta-carotene, canthaxanthin, zeaxanthin, astaxanthin and lycopene) in aqueous micellar environments have been obtained from a pulse radiolysis study of electron transfer between the carotenoids and tryptophan radical cations as a function of pH, and lie in the range of 980-1060 mV. These values are consistent with our observation that the carotenoid radical cations oxidise tyrosine and cysteine. The decays of the carotenoid radical cations in the absence of added reactants suggest a distribution of exponential lifetimes. The radicals persist for up to about 1 s, depending on the medium.
    Citation
    One-electron reduction potentials of dietary carotenoid radical cations in aqueous micellar environments. 2001, 500 (3):132-6 FEBS Lett.
    Journal
    FEBS Letters
    URI
    http://hdl.handle.net/10541/85560
    PubMed ID
    11445071
    Type
    Article
    Language
    en
    ISSN
    0014-5793
    Collections
    All Paterson Institute for Cancer Research

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