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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of nutrition 39 (2000), S. 7-11 
    ISSN: 1436-6215
    Keywords: Key wordsβ-carotene-d8– retinol-d4– humans – retinol equivalence – stable isotope – mass spectrometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Medicine
    Notes: Summary Background: Quantitative information on conversion of β-carotene to vitamin A in humans is limited. Aim of the study: Our laboratory has developed a stable isotope method for studying the conversion of β-carotene (β-C) to vitamin A. Methods: Two dosage levels (a pharmacological dose, 126.0 mg β-C-d 8, and a physiological dose, 6.0 mg β-D-d 8) were used 2.5 y apart in an adult female volunteer to study dose effects on the conversation of β-C to vitamin A. Blood samples were collected over 21 d. β-C and retinol were extracted from serum and isolated by high performance liquid chromatography. The retinol fraction was derivatized to a trimethylsilyl ether which was analyzed by gas chromatograph/mass spectrometry with electron capture negative chemical ionization. Results: The retinol-d 4 response in the circulation peaked at 24 hours after the β-C-d 8 dose, with a higher percent enrichment after the pharmacological dose than after the physiological dose. By using retinyl acetate-d 8 as the vitamin A reference, the retinol-d 4 formed from 6 mg of β-C-d 8 (11.2 μmol) was calculated to be equivalent to 1.6 mg of retinol (i. e., 3.8 mg of β-C was equivalent to 1 mg of retinol). However, the retinol-d 4 formed from 126 mg of β-C-d 8 (235 μmol) was equivalent to 2.3 mg of retinol (i. e., 55 mg β-C was equivalent to 1 mg retinol). Conclusion: These results provide evidence that it is feasibile to use stable isotope reference method to study retinol equivalence of β-C and that there may be a dose-dependence on bioconversion of β-carotene to retinol.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 23 (2000), S. 445-448 
    ISSN: 0935-6304
    Keywords: O-Aryl,O-(1-methylthioethylideneamino)phosphates ; retention prediction ; quantitative structure-retention relationship (QSRR) ; reversed-phase HPLC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Using factor analysis and stepwise linear regression methods, two parameters - CMR and ECCR - were selected from eight solute-related structure parameters as the most retention-influencing parameters. The relationships between the retention data (k ´) and the two structure parameters were established for 13 O-aryl,O-(1-methylthioethylideneamino)phosphate compounds under a wide range of experimental conditions. The retention data (k ´) of another seven compounds with similar structures were predicted using these QSRR equations. Good agreement was obtained between the experimental k ´ values and predicted ones.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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