Investigating in vitro digestion of food models to explain in vivo micronutrient bioavailability
Résumé
Introduction
A major challenge in the next years will consist in producing healthy and sustainable foods with optimized
nutritional quality. Food fortification to increase micronutrient intakes is a strategy currently
used to overcome deficiencies.
Objective
Since the structural characteristics of food influence disintegration process during digestion, it appears
relevant to assess the impact of food structure on micronutrient bioavailability.
Methodology
Four model foods have been developed and enriched in lutein and vitamin D. These products were
designed such as their composition was identical but their structures and textures were different.
Custard, pudding, sponge cake and biscuit were thus produced by modulating the production process.
A clinical trial has been set up, involving twelve healthy male subjects for a monocentric, controlled
and randomized study, in a cross experimental design. After an overnight fast, kinetics of plasma
micronutrient levels were recorded for 8 hours following each product consumption. In a second
phase, the model foods have been digested using the INFOGEST in vitro model. Kinetics of matrix
disintegration and micronutrients release have been recorded.
Main findings
The micronutrient absorption curves depended on the matrix. Especially, the biscuit resulted in a
significantly later peak of maximal absorption for both micronutrients, and a lower total bioavailability
for vitamin D. In vitro, digestion might enable to determine which food characteristics influence
matrix disintegration, thereby affecting micronutrient bioaccessibility. Indeed, markers of matrix disintegration,
namely proteolysis and lipolysis kinetics, suggested differences amongst the four model
foods.
Conclusion
The in vivo results highlight that food structure modulates the kinetics of micronutrient appearance
in plasma. Correspondences might be established between the kinetics of food matrix disintegration
during in vitro digestion and the kinetics of micronutrient absorption during the clinical study. Using
the DIDGI, a dynamic in vitro digestion model, further studies will aim to refine the quality of the
model and the results obtained.
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