| Literature DB >> 30886367 |
André Brodkorb1, Lotti Egger2, Marie Alminger3, Paula Alvito4, Ricardo Assunção4, Simon Ballance5, Torsten Bohn6, Claire Bourlieu-Lacanal7, Rachel Boutrou8, Frédéric Carrière9, Alfonso Clemente10, Milena Corredig11, Didier Dupont8, Claire Dufour12, Cathrina Edwards13, Matt Golding14, Sibel Karakaya15, Bente Kirkhus5, Steven Le Feunteun8, Uri Lesmes16, Adam Macierzanka17, Alan R Mackie18, Carla Martins4, Sébastien Marze19, David Julian McClements20, Olivia Ménard8, Mans Minekus21, Reto Portmann2, Cláudia N Santos22,23, Isabelle Souchon24, R Paul Singh25, Gerd E Vegarud26, Martin S J Wickham27, Werner Weitschies28, Isidra Recio29.
Abstract
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.Entities:
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Year: 2019 PMID: 30886367 DOI: 10.1038/s41596-018-0119-1
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491