

Volume 90, Issue 4, October (2003), pp. 795-801 © The Author 2003
doi:10.1079/BJN2003962
Medline/PubMed Citation | Related Articles in PubMed | Download to Citation Matcher
Plasma response to a single dose of dietary β-cryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in adult human subjects: a comparative study
Dietmar E. Breithaupt1, Philipp Weller1, Maike Wolters2, Andreas Hahn2 1Institute of Food Chemistry, University of Hohenheim, Garbenstr. 28, 70593 Stuttgart, Germany 2Institute of Food Science, University of Hannover, Wunstorferstr. 14, 30453 Hannover, Germany
(Received 17 December 2002Revised 22 May 2003Accepted 23 June 2003)
Many orange-coloured fruits contain β-cryptoxanthin in its non-esterified as well as its esterified form. Information concerning the absorption of β-cryptoxanthin, especially with regard to the metabolism of its fatty acid esters, is rather scarce. The present study assessed the plasma concentration reached after consumption of a single dose of native β-cryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in equal total amounts. In a randomized, single-blind crossover study, twelve subjects were served a portion of yoghurt containing esterified or non-esterified β-cryptoxanthin (1·3 mg absolute) together with a balanced breakfast. Between the two intervention days, there was a 2-week depletion period. After a fasting blood sample had been taken, futher samples were taken from the subjects at 3, 6, 9, 12 and 24 h. The concentration of non-esterified β-cryptoxanthin in the whole plasma was determined by HPLC; β-cryptoxanthin identification was confirmed by liquid chromatography–atmospheric pressure chemical ionization–MS analyses. Irrespective of the consumed diet, the plasma β-cryptoxanthin concentrations increased significantly (P=0·05) and peaked after 6–12 h. The concentration curves, as well as the areas under the curves, were not distinguishable according to two-sided F and t tests (P=0·05). Standardization of β-cryptoxanthin concentrations to plasma triacylglycerol and cholesterol had no impact on the results. Thus, the present study indicates comparable bioavailability of both non-esterified β-cryptoxanthin and mixtures of β-cryptoxanthin esters. The results support the existence of an effective enzymatic cleavage system accepting various β-cryptoxanthin esters.
Keywords: β-Cryptoxanthin, Carotenoid ester, Plasma carotenoid response, Liquid chromatography–atmospheric pressure chemical ionization–mass spectroscopy
Abbreviations: APcI, atmospheric pressure chemical ionization, AUC, area under the curve, LC, liquid chromatography, MBTE, methyl-tert-butyl ether
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