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      Mass Transfer and Nutrient Absorption in a Simulated Model of Small Intestine

      , , ,
      Journal of Food Science
      Wiley

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          Most cited references36

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          Food oral processing—A review

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            Disintegration of solid foods in human stomach.

            Knowledge of the disintegration of solid foods in human stomach is essential to assess the bioavailability of nutrients in the gastrointestinal (GI) tract. A comprehensive review of food gastric digestion, focusing on disintegration of solid foods, is presented. Most of the research reviewed in this paper is contained in the medical, pharmaceutical, food, and nutritional literature. Stomach physiology is briefly introduced, including composition and rheological properties of gastric contents, stomach wall motility in fed/fasted states, and hydrodynamic and mechanical forces that act on the ingested food. In vivo and in vitro methods used for studying food and drug digestion in GI are summarized. Stomach emptying rate, which controls the rate of absorption of nutrients, is highly related to the disintegration of foods. This topic is highlighted with focus on the important mechanisms and the influence of chemical and physical properties of foods. Future research in this area is identified to increase our fundamental understanding of the food digestion process in the stomach as related to the food composition, material properties such as texture and microstructure, and chemical characteristics. This information is necessary to develop new guidelines for seeking innovative processing methods to manufacture foods specifically targeted for health.
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              A compartmental absorption and transit model for estimating oral drug absorption.

              This report describes a compartmental absorption and transit model to estimate the fraction of dose absorbed and the rate of drug absorption for passively transported drugs in immediate release products. The model considers simultaneous small intestinal transit flow and drug absorption. Both analytical and numerical methods were utilized to solve the model equations. It was found that the fraction of dose absorbed can be estimated by F(a) = 1-(1+0.54 P(eff))(-7), where P(eff) is the human effective permeability in cm/h. A good correlation was found between the fraction of dose absorbed and the effective permeability for ten drugs covering a wide range of absorption characteristics. The model was able to explain the oral plasma concentration profiles of atenolol.
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                Author and article information

                Journal
                Journal of Food Science
                Wiley
                00221147
                August 2010
                August 2010
                July 21 2010
                : 75
                : 6
                : E339-E346
                Article
                10.1111/j.1750-3841.2010.01659.x
                20722918
                8204909e-fb73-4253-91e0-ec31fbc96613
                © 2010

                http://doi.wiley.com/10.1002/tdm_license_1.1

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