Literature DB >> 26017815

Computational Fluid Dynamics Simulation of Hydrodynamics and Stresses in the PhEur/USP Disintegration Tester Under Fed and Fasted Fluid Characteristics.

Sarah Kindgen1, Herbert Wachtel2, Bertil Abrahamsson3, Peter Langguth1.   

Abstract

Disintegration of oral solid dosage forms is a prerequisite for drug dissolution and absorption and is to a large extent dependent on the pressures and hydrodynamic conditions in the solution that the dosage form is exposed to. In this work, the hydrodynamics in the PhEur/USP disintegration tester were investigated using computational fluid dynamics (CFD). Particle image velocimetry was used to validate the CFD predictions. The CFD simulations were performed with different Newtonian and non-Newtonian fluids, representing fasted and fed states. The results indicate that the current design and operating conditions of the disintegration test device, given by the pharmacopoeias, are not reproducing the in vivo situation. This holds true for the hydrodynamics in the disintegration tester that generates Reynolds numbers dissimilar to the reported in vivo situation. Also, when using homogenized US FDA meal, representing the fed state, too high viscosities and relative pressures are generated. The forces acting on the dosage form are too small for all fluids compared to the in vivo situation. The lack of peristaltic contractions, which generate hydrodynamics and shear stress in vivo, might be the major drawback of the compendial device resulting in the observed differences between predicted and in vivo measured hydrodynamics.
© 2015 Wiley Periodicals, Inc. and the American Pharmacists Association.

Keywords:  LADME; biopharmaceutics; computational fluid dynamics; disintegration testing; food effects; hydrodynamics; in vitro models; mathematical model; oral drug delivery; solid dosage form

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Year:  2015        PMID: 26017815     DOI: 10.1002/jps.24511

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  5 in total

Review 1.  Development of In Vitro Dissolution Testing Methods to Simulate Fed Conditions for Immediate Release Solid Oral Dosage Forms.

Authors:  Timothy R Lex; Jason D Rodriguez; Lei Zhang; Wenlei Jiang; Zongming Gao
Journal:  AAPS J       Date:  2022-03-11       Impact factor: 4.009

2.  Justification of disintegration testing beyond current FDA criteria using in vitro and in silico models.

Authors:  Lukas Uebbing; Lukas Klumpp; Gregory K Webster; Raimar Löbenberg
Journal:  Drug Des Devel Ther       Date:  2017-04-11       Impact factor: 4.162

3.  Dissolution of an ensemble of differently shaped poly-dispersed drug particles undergoing solubility reduction: mathematical modelling.

Authors:  Michela Abrami; Lucia Grassi; Rosario di Vittorio; Dritan Hasa; Beatrice Perissutti; Dario Voinovich; Gabriele Grassi; Italo Colombo; Mario Grassi
Journal:  ADMET DMPK       Date:  2020-07-14

4.  Modelling and Simulation of the Drug Release from a Solid Dosage Form in the Human Ascending Colon: The Influence of Different Motility Patterns and Fluid Viscosities.

Authors:  Michael Schütt; Konstantinos Stamatopoulos; Hannah K Batchelor; Mark J H Simmons; Alessio Alexiadis
Journal:  Pharmaceutics       Date:  2021-06-10       Impact factor: 6.321

5.  Tablet Disintegration and Dispersion under In Vivo-like Hydrodynamic Conditions.

Authors:  Jan Lenz; Frederik Fuest; Jan Henrik Finke; Heike Bunjes; Arno Kwade; Michael Juhnke
Journal:  Pharmaceutics       Date:  2022-01-16       Impact factor: 6.321

  5 in total

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