In vitro digestion procedures to estimate the (micro)nutrient bio-availability of foods
- How does it work?
- What can it be used for?
- What can it not be used for?
- Related Facilities
- Further Information
|Key words||in vitro digestion, bio-availability, bio-accessibility, nutrient, carbohydrate, starch, fat, protein, allergen, vitamin, antioxidant, carotenoid, mineral|
|Completed by||KU Leuven LFT|
How does it work?
|Primary objective|| Analytical tool
In vitro digestion procedures are rapid, cost-effective and high through-put analysis methods to measure the bio-accessibility of (micro)nutrients in food systems, that is an estimation or prediction of the (micro)nutrient bio-availability in those food systems.
|Working principle|| The bio-availability of (micro)nutrients, (the fraction of ingested nutrients available for utilization in normal physiological functions or storage), depends on many host- and diet-related factors. The food matrix in which the (micro)nutrient is incorporated affects (micro)nutrient release, a critical step for (micro)nutrient absorption. In this context, the (micro)nutrient bio-accessibility has been defined as the fraction of ingested (micro)nutrients that is released from the food matrix (to mixed micelles) and thereby made available for absorption.
By simulation of human digestion, (micro)nutrient bio-accessibility can be measured in vitro. Hereto, numerous digestion models have been developed to simulate the physiological conditions and sequence of events that occur during digestion in the human gastrointestinal tract. Most of these in vitro models include an oral, gastric and intestinal phase, but the model complexity varies.
The most simple, basic models, are called static or biochemical models and involve the use of digestive enzymes (most commonly amylases, proteases and lipases) and fluids to simulate and measure the release of (micro)nutrients or the transfer of (micro)nutrients to micelles during gastric and intestinal digestion. To simulate in vivo absorption of (micro)nutrients, divers models such as Caco-2 human intestinal cells can be used. More complex, multicompartmental models, such as the TNO intestinal model (1) and the dynamic gastric model (2), take into account the dynamic character of the physiological digestion process. Recently, also models, critically taking into account mechanical disintegration during oral and gastric digestion have been developed (3, 4).
In vitro digestion procedures have been shown very useful to estimate or to predict the (micro)nutrient bio-accessibility.
|Additional effects||In vitro digestion methods are useful in the context of targeted release of bio-active micronutrients (cf. carotenoids), structural design for tailored fat digestion (cf. satiety, satiation), understanding the fate of proteins (cf. food allergy in for example GM crops) , analysis of glycaemic properties of foods…|
|Important process parameters|| Knowledge on human digestion is a prerequisite to develop an in vitro digestion procedure specific for a particular (micro)nutrient in a particular food system and an advantage to interpret results obtained by in vitro digestion tests.
Most commonly used enzymes are amylases, proteases and lipases.
|Important product parameters|
What can it be used for?
|Products||Plant-based foods, meat, fish, dairy, emulsion-based foods…|
|Operations||Product development (assessment of nutritive value)|
|Solutions for short comings|| Product development for personalized nutrition.
Cost-effective and high through-put analysis
What can it NOT be used for?
|Other limitations||These systems remain in vitro approximations of in vivo digestibility. Incomplete knowledge on human digestion processes can limit accuracy of in vitro procedures.|
|Risks or hazards|
|Maturity||Different in vitro digestion procedures (for specific (micro)nutrients in specific types of food matrices and with different degrees of complexity) are available. Continuously, models are further developed and new models are developed. Validation of different in vitro procedures under a variety of conditions and critical evaluation of the procedures could further improve the methods.|
|Modularity /Implementation||Not applicable|
|Consumer aspects||Not applicable|
|Legal aspects||Not applicable|
|Environmental aspects||Not applicable|
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|Institutes||KU Leuven LFT, IFR, TNO Institute, University of Massachusetts Amherst|
|References|| 1. Minekus, M., Marteau, P., Havenaar, R., Huis in’t Veld, J.H.J. (1995). A multicompartmental dynamic computer-controlled model simulating the stomach and small intestine. Atla, 23, 197-209.
2. Wickham, M., Faulks, R., Mills, C. (2009). In vitro digestion methods for assessing the effect of food structure on allergen breakdown. Molecular Nutrition and Food Research, 53(8), 952-958.
3. Lemmens, L., Van Buggenhout, S., Oey, I., Van Loey, A., Hendrickx, M. (2009). Towards a better understanding of the relationship between the β-carotene in vitro bio-accessibility and pectin structural changes: A case study on carrots. Food Research International, 42 (9), 1323-1330.
4. Ferrua, M.J., Kong, F., Singh, R.P. (2011). Computational modeling of gastric digestion and the role of food material properties. Trends in Food Science and Technology, 22(9), 480–491.
5. Van Buggenhout, S., Alminger, M., Lemmens, L., Colle, I., Knockaert, G., Moelants, K., Van Loey, A., Hendrickx, M. (2010). In vitro approaches to estimate the effect of food processing on carotenoid bio-availability need thorough understanding of process induced microstructural changes. Trends in Food Science and Technology, 21, 607-318.
6. Hur, S.J., Lim, B.O., Decker, E.A., McClements, D.J. (2011). In vitro human digestion models for food applications. Food Chemistry, 125, 1-12.
7. Ladics, G.S. (2008). Current codex guidelines for assessment of potential protein allergenicity. Food and Chemical Toxicology, 46 (10 SUPPL.), S20-S23.
8. Araya, H., Contreras, P., Alviña, M., Vera, G., Pak, N. (2002). A comparison between an in vitro method to determine carbohydrate digestion rate and the glycemic response in young men. European Journal of Clinical Nutrition, 56, 735-739.
Knowledge on human digestion is a prerequisite to develop an in vitro digestion procedure specific for a particular (micro)nutrient in a particular food system and an advantage to interpret results obtained by in vitro digestion tests. Most commonly used enzymes are amylases, proteases and lipases.warning.png"Knowledge on human digestion is a prerequisite to develop an in vitro digestion procedure specific for a particular (micro)nutrient in a particular food system and an advantage to interpret results obtained by in vitro digestion tests. Most commonly used enzymes are amylases, proteases and lipases." cannot be used as a page name in this wiki.