Can Changes in Hydrophobicity Increase the Bioavailability of Alpha-tocopherol?
Overview
Affiliations
Background: Bioavailability of fat-soluble vitamins from conventional oral supplements is insufficient in some conditions in which fat digestion and absorption are chronically impaired (e. g. cystic fibrosis).
Aim Of The Study: We used a water-soluble form of fatsoluble vitamin E (AQUANOVA solubilisate) to create a nutritional supplement (NS) in the form of vitaminized gummi bears (with micellised water-soluble alpha-tocopheryl acetate (100 IU) and 400 mg crystalline vitamin C). We assessed the bioavailability of the NS in comparison to conventional preparations.
Methods: The trial consisted of three study days (d0: NS sucked; d10: NS swallowed; d20: reference products swallowed). A total of 14 subjects (6 male/8 female), aged 25.3 (22.7-35.3) years, BMI 24.3 (19.0-31.7) kg/m(2) participated in the study. They had blood samples drawn after fasting for >or=12 hours and then 1, 5, 15, 30, 60, 120, 180, 240, 300 and 320 minutes after ingesting the vitamins. HPLC and a colorimetric method were used to determine vitamin E and vitamin C, respectively. Areas under the curve (AUC(0-320min)) and maximum increases in plasma concentrations (Delta concentration) were calculated to assess bioavailability.
Results: The AUCs(0-320min) of alpha-tocopherol from d0 were significantly larger (p = 0.016) when compared to d20. Moreover, the maximum increase in alpha-tocopherol plasma concentrations was significantly higher for d0 (p = 0.023) and d10 (p = 0.002) when compared to d20.
Conclusions: Short-term bioavailability of AQUANOVA micellised fat-soluble vitamin E from our NS was significantly higher than from regular supplements. The NS will now be tested for its clinical efficacy in a randomized double-blind controlled intervention trial with CF patients.
Li L, Zeng Y, Chen M, Liu G Polymers (Basel). 2022; 14(16).
PMID: 36015535 PMC: 9415603. DOI: 10.3390/polym14163278.
Mosseler A, Schmicke M, Holtershinken M, Beyerbach M, Kamphues J Int J Mol Sci. 2016; 17(10).
PMID: 27690005 PMC: 5085675. DOI: 10.3390/ijms17101642.
Saiki R, Lunceford A, Bixler T, Dang P, Lee W, Furukawa S Aging Cell. 2008; 7(3):291-304.
PMID: 18267002 PMC: 3104051. DOI: 10.1111/j.1474-9726.2008.00378.x.