Effect of aggregation form on bioavailability of zeaxanthin in humans: a randomised cross-over study

• Published in: British journal of nutrition Vol. 118; no. 9; pp. 698 - 706
• Main Authors: Hempel, Judith, Fischer, Anja, Fischer, Monique, Högel, Josef, Bosy-Westphal, Anja, Carle, Reinhold, Schweiggert, Ralf M.
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 14.11.2017
• Subjects: Adult; Agglomeration; Bioavailability; Biological Availability; Body Mass Index; Brain; Carotenoids; Cholesterol; Chromatography; Computational fluid dynamics; Cross-Over Studies; Crossovers; Deposition; Dietary Supplements; Digestion; duodenal juices; encapsulation; eyes; Fasting; Female; Food; Food plants; Formulations; Human and Clinical Nutrition; Human subjects; Humans; Hydrogen bonds; in vitro digestion; In vivo methods and tests; lipoproteins; Lycium - chemistry; Male; Palmitates; Randomization; Simulation; Single-Blind Method; test meals; Xanthophylls; Young Adult; Zeaxanthin; Zeaxanthins - administration & dosage; Zeaxanthins - blood; Zeaxanthins - pharmacokinetics; United States > US; H-aggregates; Carotenoids; Food matrix; J-aggregates; Supplements; MTBE methyl tert-butyl ether; TRL TAG-rich lipoprotein
• ISSN: 0007-1145; 1475-2662; 1475-2662
• DOI: 10.1017/S0007114517002653

Carotenoid bioavailability from plant and animal food is highly variable depending on numerous factors such as the physical deposition form of carotenoids. As the carotenoid zeaxanthin is believed to play an important role in eye and brain health, we sought to compare the human bioavailability of an H-aggregated with that of a J-aggregated deposition form of zeaxanthin encapsulated into identical formulation matrices. A randomised two-way cross-over study with sixteen participants was designed to compare the post-prandial bioavailability of an H-aggregated zeaxanthin and a J-aggregated zeaxanthin dipalmitate formulation, both delivering 10 mg of free zeaxanthin. Carotenoid levels in TAG-rich lipoprotein fractions were analysed over 9·5 h after test meal consumption. Bioavailability from the J-aggregated formulation (AUC=55·9 nmol h/l) was 23 % higher than from the H-aggregated one (AUC=45·5 nmol h/l), although being only marginally significant (P=0·064). Furthermore, the same formulations were subjected to an internationally recognised in vitro digestion protocol to reveal potential strengths and weaknesses of simulated digestions. In agreement with our human study, liberation of zeaxanthin from the J-aggregated formulation into the simulated duodenal fluids was superior to that from the H-aggregated form. However, micellization rate (bioaccessibility) of the J-aggregated zeaxanthin dipalmitate was lower than that of the H-aggregated zeaxanthin, being contradictory to our in vivo results. An insufficient ester cleavage during simulated digestion was suggested to be the root cause for these observations. In brief, combining our in vitro and in vivo observations, the effect of the different aggregation forms on human bioavailability was lower than expected.