The application of the GastroDuo as an in vitro dissolution tool to simulate the gastric emptying of the postprandial stomach.

In the postprandial stomach, processes such as secretion, digestion, and gastric emptying all occur simultaneously. Therefore, the system is highly heterogeneous and dynamically changing, for instance in terms of various physicochemical parameters such as pH value or viscosity. Thus, the administration of a drug together with food can result in highly variable drug plasma concentrations, which may affect the efficacy and safety of the pharmacotherapy. In this work, pharmacokinetic data obtained from two fed state bioequivalence studies with the immediate release drug products Viagra® (sildenafil) and Adenuric® (febuxostat) have been analyzed. This evaluation revealed that basically three characteristic types of onset behavior of drug plasma concentration can be distinguished. It was hypothesized that the different types of onset behavior were mainly caused by the interplay between gastric drug dissolution and gastric emptying. To study this interplay in vitro, a biopredictive dissolution tool the GastroDuo was developed and used for both drug products. Thereby, three different test programs have been applied to simulate certain aspects of the postprandial human stomach, which included dynamic pH changes, gastric peristalsis and the kinetics of gastric emptying. Specifically, the behavior of non caloric fluids by the so called "Magenstrasse" was taken into deeper consideration. The experiments revealed that the dissolution and emptying behavior of the two drug products were affected in different ways by the three test programs. The in vitro data nicely explained the tendencies of the drug products for certain types of onset behavior observed in the pharmacokinetic data. Whereas Viagra® was stronger affected by simulated peristalsis, Adenuric® was more sensitive to the simulated emptying kinetics. This work clearly demonstrated the important role of gastric fluid emptying for the onset of drug plasma concentration after oral administration of immediate release formulations in the fed state. Moreover, this was the first study in which the GastroDuo was applied as a biopredictive in vitro model which is able to simulate crucial parameters of the human stomach (e.g. pH profiles, gastric emptying) in a realistic manner.

[1]  W. Weitschies,et al.  Effect of Coadministered Water on the In Vivo Performance of Oral Formulations Containing N-Acetylcysteine: An In Vitro Approach Using the Dynamic Open Flow-Through Test Apparatus. , 2017, Molecular pharmaceutics.

[2]  J. Malagelada,et al.  Different gastric, pancreatic, and biliary responses to solid-liquid or homogenized meals , 1979, Digestive Diseases and Sciences.

[3]  D. Fleisher,et al.  Drug, Meal and Formulation Interactions Influencing Drug Absorption After Oral Administration , 1999, Clinical pharmacokinetics.

[4]  M. Grimm,et al.  Resolving the physiological conditions in bioavailability and bioequivalence studies: Comparison of fasted and fed state. , 2016, European journal of pharmaceutics and biopharmaceutics.

[5]  J. Malagelada Quantificantion of gastric solid-liquid discrimination during digestion of ordinary meals. , 1977, Gastroenterology.

[6]  W. Weitschies,et al.  In vitro simulation of realistic gastric pressure profiles , 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[7]  K. Schulze Imaging and modelling of digestion in the stomach and the duodenum , 2006, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

[8]  S. Sriwiriyajan,et al.  Effect of omeprazole on the pharmacokinetics of itraconazole , 1998, European Journal of Clinical Pharmacology.

[9]  James G Brasseur,et al.  A stomach road or "Magenstrasse" for gastric emptying. , 2007, Journal of biomechanics.

[10]  M. Grimm,et al.  Investigation of pH and Temperature Profiles in the GI Tract of Fasted Human Subjects Using the Intellicap(®) System. , 2015, Journal of pharmaceutical sciences.

[11]  A. Dowson,et al.  Speed of Onset and Efficacy of Zolmitriptan Nasal Spray in the Acute Treatment of Migraine , 2003, CNS drugs.

[12]  Michael Grimm,et al.  Gastric Water Emptying under Fed State Clinical Trial Conditions Is as Fast as under Fasted Conditions. , 2017, Molecular pharmaceutics.

[13]  L. Marciani,et al.  Assessment of antral grinding of a model solid meal with echo-planar imaging. , 2001, American journal of physiology. Gastrointestinal and liver physiology.

[14]  C. V. van Herpen,et al.  Effect of food and acid-reducing agents on the absorption of oral targeted therapies in solid tumors. , 2016, Drug discovery today.

[15]  Lutz Trahms,et al.  Impact of the intragastric location of extended release tablets on food interactions. , 2005, Journal of controlled release : official journal of the Controlled Release Society.

[16]  M. Camilleri Integrated upper gastrointestinal response to food intake. , 2006, Gastroenterology.

[17]  J. Kühn,et al.  Intragastric volume changes after intake of a high-caloric, high-fat standard breakfast in healthy human subjects investigated by MRI. , 2014, Molecular pharmaceutics.

[18]  W. Weitschies,et al.  Bio-relevant dissolution testing of hard capsules prepared from different shell materials using the dynamic open flow through test apparatus. , 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[19]  J. Blanchard,et al.  The absolute bioavailability of caffeine in man , 2004, European Journal of Clinical Pharmacology.

[20]  Martin C Garnett,et al.  Quantification of gastrointestinal liquid volumes and distribution following a 240 mL dose of water in the fasted state. , 2014, Molecular pharmaceutics.

[21]  R. Singh,et al.  Disintegration of solid foods in human stomach. , 2008, Journal of food science.

[22]  Bart Hens,et al.  Supersaturation and Precipitation of Posaconazole Upon Entry in the Upper Small Intestine in Humans. , 2015, Journal of pharmaceutical sciences.

[23]  Werner Weitschies,et al.  Development of a bio-relevant dissolution test device simulating mechanical aspects present in the fed stomach. , 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[24]  L. Trahms,et al.  Bioavailability of amoxicillin and clavulanic acid from extended release tablets depends on intragastric tablet deposition and gastric emptying. , 2008, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[25]  Michael Grimm,et al.  Navigating the human gastrointestinal tract for oral drug delivery: Uncharted waters and new frontiers. , 2016, Advanced drug delivery reviews.

[26]  A. Fox Onset of Effect of 5‐HT1B/1D Agonists: A Model With Pharmacokinetic Validation , 2004, Headache.

[27]  B. Abrahamsson,et al.  Food effects on tablet disintegration. , 2004, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[28]  M. Grimm,et al.  Intragastric pH and pressure profiles after intake of the high-caloric, high-fat meal as used for food effect studies. , 2015, Journal of controlled release : official journal of the Controlled Release Society.

[29]  M. Karsdal,et al.  Optimizing bioavailability of oral administration of small peptides through pharmacokinetic and pharmacodynamic parameters: The effect of water and timing of meal intake on oral delivery of Salmon Calcitonin , 2008, BMC clinical pharmacology.