Reaction and Scavenging Mechanism of β-Carotene and Zeaxanthin with Reactive Oxygen Species
In order to investigate chemical scavenging mechanism of singlet oxygen, superoxide anion radical, and hydroxyl radical by carotenoids, reaction products obtained by reacting β-carotene or zeaxanthin with singlet oxygen, superoxide anion radical, and hydroxyl radical were analyzed by LC/PDA ESI-MS,...
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Veröffentlicht in: | Journal of Oleo Science 2017, Vol.66(1), pp.77-84 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | In order to investigate chemical scavenging mechanism of singlet oxygen, superoxide anion radical, and hydroxyl radical by carotenoids, reaction products obtained by reacting β-carotene or zeaxanthin with singlet oxygen, superoxide anion radical, and hydroxyl radical were analyzed by LC/PDA ESI-MS, and ESR spectrometry. β-Carotene endoperoxides were identified as the major reaction products of β-carotene and singlet oxygen, while β-carotene epoxides were the major reaction products of β-carotene and superoxide anion or hydroxyl radical. Similar results to those for β-carotene were obtained with zeaxanthin. |
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ISSN: | 1345-8957 1347-3352 |
DOI: | 10.5650/jos.ess16107 |