TY - JOUR
T1 - Vitamine and vitamine acetate absorption from self-assembly systems under pancreas insufficiency conditions
AU - Nagy, Kornél
AU - Lobo, Beatriz
AU - Courtet-Compondu, Marie Claude
AU - Braga-Lagache, Sophie
AU - Ramos, Laura
AU - Puig-Divi, Valentí
AU - Azpiroz, Fernando
AU - Malagelada, Juan Ramón
AU - Beaumont, Maurice
AU - Moulin, Julie
AU - Acquistapacea, Simone
AU - Sagalowicz, Laurent
AU - Kussmann, Martin
AU - Santos, Javier
AU - Holst, Birgit
AU - Williamson, Gary
PY - 2014/3/1
Y1 - 2014/3/1
N2 - We determined the bioavailability of vitamin E from self-assembly structures in patients with diagnosed chronic pancreas insufficiency. Vitamin E solubilized in dispersed inverted bicontinuous cubic phase and in micellar formulation was delivered directly to the small intestine by tube-feeding. A cross-over study with randomization of 6 subjects and 2 treatments including a combined dose of 18 mg (27 IU) of vitamin E (RRR-[5,7-methyl-(2H 6)]- a-tocopherol) and 27 mg (27 IU) vitamin E acetate (RRR-[5-methyl-2H3]-α-tocopheryl acetate) was applied over a time period of 1 h. Plasma samples were collected for 56 h and analyzed by liquid chromatography-mass spectrometry. Appearance of labeled tocopherols originating from the treatment started at 25 h and reached C max (0.6-4.6 μM depending on subject) in the 7-9 h window. From the Tmax onwards, both forms of tocopherols diminished slowly to 30-50% of their maxima within 56 h. Strong inter-individual variation was observed in the plasma appearance curves (relative standard deviation varied between 38-45%). No significant discrimination was found between the absorption of free or acetylated forms of deuterated a-tocopherol confirming that application of acetylated a-tocopherol provides the same bioavailability as free a-tocopherol. This observation is valid in both dispersed inverted bicontinuous cubic phase and micellar formulations. Furthermore, since the area-underthe- curve values from cubic phase and from micellar formulations are similar, the cubic phase formulation could represent an alternative delivery system for lipophilic micronutrients in conditions or studies where polysorbatebased micelles cannot be generated. © Schweizerische Chemische Gesellschaft.
AB - We determined the bioavailability of vitamin E from self-assembly structures in patients with diagnosed chronic pancreas insufficiency. Vitamin E solubilized in dispersed inverted bicontinuous cubic phase and in micellar formulation was delivered directly to the small intestine by tube-feeding. A cross-over study with randomization of 6 subjects and 2 treatments including a combined dose of 18 mg (27 IU) of vitamin E (RRR-[5,7-methyl-(2H 6)]- a-tocopherol) and 27 mg (27 IU) vitamin E acetate (RRR-[5-methyl-2H3]-α-tocopheryl acetate) was applied over a time period of 1 h. Plasma samples were collected for 56 h and analyzed by liquid chromatography-mass spectrometry. Appearance of labeled tocopherols originating from the treatment started at 25 h and reached C max (0.6-4.6 μM depending on subject) in the 7-9 h window. From the Tmax onwards, both forms of tocopherols diminished slowly to 30-50% of their maxima within 56 h. Strong inter-individual variation was observed in the plasma appearance curves (relative standard deviation varied between 38-45%). No significant discrimination was found between the absorption of free or acetylated forms of deuterated a-tocopherol confirming that application of acetylated a-tocopherol provides the same bioavailability as free a-tocopherol. This observation is valid in both dispersed inverted bicontinuous cubic phase and micellar formulations. Furthermore, since the area-underthe- curve values from cubic phase and from micellar formulations are similar, the cubic phase formulation could represent an alternative delivery system for lipophilic micronutrients in conditions or studies where polysorbatebased micelles cannot be generated. © Schweizerische Chemische Gesellschaft.
KW - Bioavailability
KW - Chronic pancreas insufficiency
KW - Self-assembly systems
KW - Vitamin E
U2 - 10.2533/chimia.2014.129
DO - 10.2533/chimia.2014.129
M3 - Article
SN - 0009-4293
VL - 68
SP - 129
EP - 134
JO - Chimia
JF - Chimia
IS - 3
ER -