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Journal of Lipid Research, Vol 25, 638-645, Copyright © 1984 by Lipid Research, Inc.
JB Williams, BC Pramanik and JL Napoli
High-performance liquid chromatography systems were developed to rapidly
separate retinol from its esters, analyze the total spectrum of neutral
vitamin A compounds, and purify retinyl esters to homogeneity. Chemical
ionization mass spectrometric techniques were used to identify vitamin A
compounds; these techniques are also applicable to quantification of tissue
vitamin A compounds. These methods provide rapid and sensitive techniques
for separation and quantification of neutral retinol metabolites. Their
utility was demonstrated by analysis of vitamin A metabolites in rat
tissues under steady-state conditions. Tissue specificity was noted for the
concentrations of retinol and its long-chain fatty acid esters, the ratio
of retinol to retinyl esters, and the fatty acid composition of retinyl
esters. Quantitatively minor amounts of several neutral polar retinol
metabolites were detected, but neither 13-cis-retinol nor 4-hydroxyretinol
was observed in vivo as metabolites of retinol in kidney.
ARTICLES
Vitamin A metabolism: analysis of steady-state neutral metabolites in rat tissues
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