Determination of α-,γ(+β)-, and δ-tocopherols in a variety of liver tissues by reverse-phase high pressure liquid chromatography


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rsaborowski [ at ] awi-bremerhaven.de

Abstract

A modified version of a previously published extraction technique using acetone as the extracting medium and separation on an HPLC equipped with a Spherisorb C18 ODS2 column packed with 3 μm particles along with a suitable flow rate and mobile phase significantly improves the resolution of the chromatographic output (fluorescence detector), allowing for accurate measurement of α-, δ- and γ(+ β)-tocopherols. It was found that two extractions of the same sample yielded approximately 97% of the total extractable α-tocopherol. Vitamin C was not needed as an anti-oxidant to protect α-tocopherol during extraction from chicken liver but was needed when using fish liver, α-tocopherol was found not to be evenly distributed in beef, chicken or fish liver. Copyright © 1996 Elsevier Science Inc.



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Eprint ID
3750
DOI https://www.doi.org/10.1016/0305-0491(96)02010-x

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Koprivnjak, J. F. , Lum, K. , Sisak, M. and Saborowski, R. (1996): Determination of α-,γ(+β)-, and δ-tocopherols in a variety of liver tissues by reverse-phase high pressure liquid chromatography , Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 113 (1), pp. 143-148 . doi: https://www.doi.org/10.1016/0305-0491(96)02010-x


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