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In vitro models for the prediction of in vivo performance of oral dosage forms.
Kostewicz, Edmund S; Abrahamsson, Bertil; Brewster, Marcus; Brouwers, Joachim; Butler, James; Carlert, Sara; Dickinson, Paul A; Dressman, Jennifer; Holm, René; Klein, Sandra; Mann, James; McAllister, Mark; Minekus, Mans; Muenster, Uwe; Müllertz, Anette; Verwei, Miriam; Vertzoni, Maria; Weitschies, Werner; Augustijns, Patrick.
Afiliação
  • Kostewicz ES; Institute of Pharmaceutical Technology, Goethe University, Frankfurt/Main, Germany.
  • Abrahamsson B; Department of Global Medicines Development, AstraZeneca R&D, S-431 83 Mölndal, Sweden.
  • Brewster M; Drug Product Development, Pharmaceutical Development and Manufacturing Sciences, Janssen Research and Development, Johnson & Johnson, Beerse, Belgium.
  • Brouwers J; Drug Delivery and Disposition, KU Leuven, Leuven, Belgium.
  • Butler J; Product Development, GlaxoSmithKline R&D, Harlow, United Kingdom.
  • Carlert S; Department of Global Medicines Development, AstraZeneca R&D, S-431 83 Mölndal, Sweden.
  • Dickinson PA; Clinical Pharmacology and Pharmacometrics, AstraZeneca R&D, Alderley Park, Macclesfield SK10 4TG, United Kingdom.
  • Dressman J; Institute of Pharmaceutical Technology, Goethe University, Frankfurt/Main, Germany.
  • Holm R; Biologics and Pharmaceutical Science, H.Lundbeck A/S, Ottiliavej 9, DK 2500 Valby, Denmark.
  • Klein S; Biopharmaceutics and Pharmaceutical Technology, University of Greifswald, Greifswald, Germany.
  • Mann J; Development Laboratories, MSD, Hoddesdon, United Kingdom.
  • McAllister M; Drug Product Design, Pfizer PGRD, Sandwich, Kent CT13 9NJ, United Kingdom.
  • Minekus M; TNO, Zeist, The Netherlands.
  • Muenster U; Material Science and Early Characterization, Research Center Aprath, Bayer Pharma AG, Germany.
  • Müllertz A; Pharmaceutical Design and Drug Delivery, University of Copenhagen, Denmark.
  • Verwei M; TNO, Zeist, The Netherlands.
  • Vertzoni M; Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopolis, 15771 Athens, Greece.
  • Weitschies W; Biopharmaceutics and Pharmaceutical Technology, University of Greifswald, Greifswald, Germany.
  • Augustijns P; Drug Delivery and Disposition, KU Leuven, Leuven, Belgium. Electronic address: patrick.augustijns@pharm.kuleuven.be.
Eur J Pharm Sci ; 57: 342-66, 2014 Jun 16.
Article em En | MEDLINE | ID: mdl-23988843
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biofarmácia / Farmacocinética / Preparações Farmacêuticas / Modelos Biológicos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biofarmácia / Farmacocinética / Preparações Farmacêuticas / Modelos Biológicos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article