INFOGEST static in vitro simulation of gastrointestinal food digestion

Статическая модель INFOGEST для моделирования переваривания пищевых продуктов in vitro в желудочно-кишечном тракте
Martin Wickham, Bente Kirkhus, Reto Portmann, Torsten Bohn, Didier Dupont, Alan R. Mackie, André Brodkorb, Werner Weitschies, Claire Bourlieu‐Lacanal, Rachel Boutrou, Steven Le Feunteun, Ricardo Assunção, David Julian McClements, Gerd E. Vegarud, Mans Minekus, Marie Alminger, Paula Alvito, Simon Ballance, Frédéric Carrière, Milena Corredig, Claire Dufour, Lotti Egger, Matt Golding, Sibel Karakaya, Uri Lesmes, Adam Macierzanka, Sébastien Marze, Olivia Ménard, Isidra Recio, Cláudia Nunes dos Santos, R. Paul Singh, Alfonso Clemente, Cathrina H. Edwards, Carla Martins, Isabelle Souchon
2019-03-18

COST INFOGEST protocolINFOGEST 2.0food matrix micronutrient releasegastrointestinal food digestionstatic in vitro digestion
Developing a mechanistic understanding of the impact of food structure and composition on human health has increasingly involved simulating digestion in the upper gastrointestinal tract. These simulations have used a wide range of different conditions that often have very little physiological relevance, and this impedes the meaningful comparison of results. The standardized protocol presented here is based on an international consensus developed by the COST INFOGEST network. The method is designed to be used with standard laboratory equipment and requires limited experience to encourage a wide range of researchers to adopt it. It is a static digestion method that uses constant ratios of meal to digestive fluids and a constant pH for each step of digestion. This makes the method simple to use but not suitable for simulating digestion kinetics. Using this method, food samples are subjected to sequential oral, gastric and intestinal digestion while parameters such as electrolytes, enzymes, bile, dilution, pH and time of digestion are based on available physiological data. This amended and improved digestion method (INFOGEST 2.0) avoids challenges associated with the original method, such as the inclusion of the oral phase and the use of gastric lipase. The method can be used to assess the endpoints resulting from digestion of foods by analyzing the digestion products (e.g., peptides/amino acids, fatty acids, simple sugars) and evaluating the release of micronutrients from the food matrix. The whole protocol can be completed in ~7 d, including ~5 d required for the determination of enzyme activities.
1
INFOGEST 2.0 uses standard laboratory equipment and requires limited expertise, facilitating broader adoption and meaningful comparison across studies.
2
The INFOGEST 2.0 protocol standardizes static upper-gastrointestinal digestion simulations using internationally agreed physiological conditions.
3
The method sequentially models oral, gastric, and intestinal digestion, incorporating physiological electrolytes, enzymes, bile, dilution, pH, and digestion times.
4
The protocol enables analysis of digestion products and micronutrient release from food matrices, and can be completed in approximately seven days including enzyme-activity measurements.
5
The static design maintains constant meal-to-fluid ratios and pH within each phase, simplifying implementation but preventing simulation of digestion kinetics.

food samples subjected to simulated upper gastrointestinal digestion

digestion products and micronutrient release resulting from sequential oral, gastric, and intestinal digestion under standardized physiological conditions

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2019-03-18
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Authors
Martin Wickham
Bente Kirkhus
Reto Portmann
Torsten Bohn
Didier Dupont
Alan R. Mackie
André Brodkorb
Werner Weitschies
Claire Bourlieu‐Lacanal
Rachel Boutrou
Steven Le Feunteun
Ricardo Assunção
David Julian McClements
Gerd E. Vegarud
Mans Minekus
Marie Alminger
Paula Alvito
Simon Ballance
Frédéric Carrière
Milena Corredig
Claire Dufour
Lotti Egger
Matt Golding
Sibel Karakaya
Uri Lesmes
Adam Macierzanka
Sébastien Marze
Olivia Ménard
Isidra Recio
Cláudia Nunes dos Santos
R. Paul Singh
Alfonso Clemente
Cathrina H. Edwards
Carla Martins
Isabelle Souchon
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