Literature DB >> 23988843

In vitro models for the prediction of in vivo performance of oral dosage forms.

Edmund S Kostewicz1, Bertil Abrahamsson2, Marcus Brewster3, Joachim Brouwers4, James Butler5, Sara Carlert2, Paul A Dickinson6, Jennifer Dressman1, René Holm7, Sandra Klein8, James Mann9, Mark McAllister10, Mans Minekus11, Uwe Muenster12, Anette Müllertz13, Miriam Verwei11, Maria Vertzoni14, Werner Weitschies8, Patrick Augustijns15.   

Abstract

Accurate prediction of the in vivo biopharmaceutical performance of oral drug formulations is critical to efficient drug development. Traditionally, in vitro evaluation of oral drug formulations has focused on disintegration and dissolution testing for quality control (QC) purposes. The connection with in vivo biopharmaceutical performance has often been ignored. More recently, the switch to assessing drug products in a more biorelevant and mechanistic manner has advanced the understanding of drug formulation behavior. Notwithstanding this evolution, predicting the in vivo biopharmaceutical performance of formulations that rely on complex intraluminal processes (e.g. solubilization, supersaturation, precipitation…) remains extremely challenging. Concomitantly, the increasing demand for complex formulations to overcome low drug solubility or to control drug release rates urges the development of new in vitro tools. Development and optimizing innovative, predictive Oral Biopharmaceutical Tools is the main target of the OrBiTo project within the Innovative Medicines Initiative (IMI) framework. A combination of physico-chemical measurements, in vitro tests, in vivo methods, and physiology-based pharmacokinetic modeling is expected to create a unique knowledge platform, enabling the bottlenecks in drug development to be removed and the whole process of drug development to become more efficient. As part of the basis for the OrBiTo project, this review summarizes the current status of predictive in vitro assessment tools for formulation behavior. Both pharmacopoeia-listed apparatus and more advanced tools are discussed. Special attention is paid to major issues limiting the predictive power of traditional tools, including the simulation of dynamic changes in gastrointestinal conditions, the adequate reproduction of gastrointestinal motility, the simulation of supersaturation and precipitation, and the implementation of the solubility-permeability interplay. It is anticipated that the innovative in vitro biopharmaceutical tools arising from the OrBiTo project will lead to improved predictions for in vivo behavior of drug formulations in the GI tract.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Biorelevant; In vitro evaluation; In vivo biopharmaceutical performance; Innovative Medicines Initiative (IMI); Oral Biopharmaceutical Tools (OrBiTo); Oral drug formulations

Mesh:

Substances:

Year:  2013        PMID: 23988843     DOI: 10.1016/j.ejps.2013.08.024

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  35 in total

1.  Food Effect in Humans: Predicting the Risk Through In Vitro Dissolution and In Vivo Pharmacokinetic Models.

Authors:  Neil Mathias; Yan Xu; Balvinder Vig; Umesh Kestur; Amy Saari; John Crison; Divyakant Desai; Aditya Vanarase; Munir Hussain
Journal:  AAPS J       Date:  2015-05-02       Impact factor: 4.009

2.  Application of Absorption Modeling in Rational Design of Drug Product Under Quality-by-Design Paradigm.

Authors:  Filippos Kesisoglou; Amitava Mitra
Journal:  AAPS J       Date:  2015-05-22       Impact factor: 4.009

3.  Assessment of In Vivo Clinical Product Performance of a Weak Basic Drug by Integration of In Vitro Dissolution Tests and Physiologically Based Absorption Modeling.

Authors:  Xuan Ding; Ivelina Gueorguieva; James A Wesley; Lee J Burns; Carrie A Coutant
Journal:  AAPS J       Date:  2015-07-01       Impact factor: 4.009

4.  Demonstrating comparative in vitro bioequivalence for animal drug products through chemistry and manufacturing controls and physicochemical characterization: a proposal.

Authors:  Marilyn N Martinez; Raafat Fahmy
Journal:  AAPS J       Date:  2015-01-22       Impact factor: 4.009

5.  "Development of Fixed Dose Combination Products" Workshop Report: Considerations of Gastrointestinal Physiology and Overall Development Strategy.

Authors:  Bart Hens; Maura Corsetti; Marival Bermejo; Raimar Löbenberg; Pablo M González; Amitava Mitra; Divyakant Desai; Dakshina Murthy Chilukuri; Alexis Aceituno
Journal:  AAPS J       Date:  2019-06-06       Impact factor: 4.009

6.  Biorelevant in vitro performance testing of orally administered dosage forms-workshop report.

Authors:  Christos Reppas; Horst-Dieter Friedel; Amy R Barker; Lucinda F Buhse; Todd L Cecil; Susanne Keitel; Johannes Kraemer; J Michael Morris; Vinod P Shah; Mary P Stickelmeyer; Chikako Yomota; Cynthia K Brown
Journal:  Pharm Res       Date:  2014-03-19       Impact factor: 4.200

Review 7.  Nanoparticles for oral delivery: Design, evaluation and state-of-the-art.

Authors:  Abhijit A Date; Justin Hanes; Laura M Ensign
Journal:  J Control Release       Date:  2016-06-09       Impact factor: 9.776

8.  Determining the polymer threshold amount for achieving robust drug release from HPMC and HPC matrix tablets containing a high-dose BCS class I model drug: in vitro and in vivo studies.

Authors:  Uroš Klančar; Saša Baumgartner; Igor Legen; Polona Smrdel; Nataša Jeraj Kampuš; Dejan Krajcar; Boštjan Markun; Klemen Kočevar
Journal:  AAPS PharmSciTech       Date:  2014-10-18       Impact factor: 3.246

Review 9.  Lipid-associated oral delivery: Mechanisms and analysis of oral absorption enhancement.

Authors:  Oljora Rezhdo; Lauren Speciner; Rebecca Carrier
Journal:  J Control Release       Date:  2016-08-09       Impact factor: 9.776

10.  A Focused Screen Identifies Antifolates with Activity on Mycobacterium tuberculosis.

Authors:  Anuradha Kumar; Ana Guardia; Gonzalo Colmenarejo; Esther Pérez; Ruben R Gonzalez; Pedro Torres; David Calvo; Ruben M Gómez; Fátima Ortega; Elena Jiménez; Raquel C Gabarro; Joaquín Rullás; Lluis Ballell; David R Sherman
Journal:  ACS Infect Dis       Date:  2015-08-12       Impact factor: 5.084

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