Literature DB >> 24643933

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

Christos Reppas1, 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.   

Abstract

Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have been utilized to decrease the number of in vivo studies required during the drug development process and to mitigate the risk related to in vivo bioequivalence studies. This report reviews the ability of current in vitro performance tests to predict in vivo performance and generate successful in vitro and in vivo correlations for oral dosage forms. It also summarizes efforts to improve the predictability of biorelevant tests. The report is based on the presentations at the 2013 workshop, Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms, in Washington, DC, sponsored by the FIP Dissolution/Drug Release Focus Group in partnership with the American Association of Pharmaceutical Scientists (AAPS) and a symposium at the AAPS 2012 Annual meeting on the same topic.

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Year:  2014        PMID: 24643933     DOI: 10.1007/s11095-014-1348-9

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  28 in total

1.  Comparison of the rates of disintegration, gastric emptying, and drug absorption following administration of a new and a conventional paracetamol formulation, using gamma scintigraphy.

Authors:  Kilian Kelly; Bridget O'Mahony; Blythe Lindsay; Tamara Jones; Tim J Grattan; Amin Rostami-Hodjegan; Howard N E Stevens; Clive G Wilson
Journal:  Pharm Res       Date:  2003-10       Impact factor: 4.200

2.  Food effects on tablet disintegration.

Authors:  Bertil Abrahamsson; Tamsin Albery; Anna Eriksson; Ingrid Gustafsson; Marie Sjöberg
Journal:  Eur J Pharm Sci       Date:  2004-06       Impact factor: 4.384

3.  Comparison and analysis of theoretical models for diffusion-controlled dissolution.

Authors:  Yanxing Wang; Bertil Abrahamsson; Lennart Lindfors; James G Brasseur
Journal:  Mol Pharm       Date:  2012-04-17       Impact factor: 4.939

4.  Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans.

Authors:  Yasushi Shono; Ekarat Jantratid; Filippos Kesisoglou; Christos Reppas; Jennifer B Dressman
Journal:  Eur J Pharm Biopharm       Date:  2010-06-01       Impact factor: 5.571

5.  Gastric flow and mixing studied using computer simulation.

Authors:  Anupam Pal; Keshavamurthy Indireshkumar; Werner Schwizer; Bertil Abrahamsson; Michael Fried; James G Brasseur
Journal:  Proc Biol Sci       Date:  2004-12-22       Impact factor: 5.349

Review 6.  PBPK models for the prediction of in vivo performance of oral dosage forms.

Authors:  Edmund S Kostewicz; Leon Aarons; Martin Bergstrand; Michael B Bolger; Aleksandra Galetin; Oliver Hatley; Masoud Jamei; Richard Lloyd; Xavier Pepin; Amin Rostami-Hodjegan; Erik Sjögren; Christer Tannergren; David B Turner; Christian Wagner; Werner Weitschies; Jennifer Dressman
Journal:  Eur J Pharm Sci       Date:  2013-09-21       Impact factor: 4.384

7.  An in vitro methodology for forecasting luminal concentrations and precipitation of highly permeable lipophilic weak bases in the fasted upper small intestine.

Authors:  Dimitrios Psachoulias; Maria Vertzoni; James Butler; David Busby; Moira Symillides; Jennifer Dressman; Christos Reppas
Journal:  Pharm Res       Date:  2012-08-14       Impact factor: 4.200

8.  Irregular absorption profiles observed from diclofenac extended release tablets can be predicted using a dissolution test apparatus that mimics in vivo physical stresses.

Authors:  Grzegorz Garbacz; Ralph-Steven Wedemeyer; Stefan Nagel; Thomas Giessmann; Hubert Mönnikes; Clive G Wilson; Werner Siegmund; Werner Weitschies
Journal:  Eur J Pharm Biopharm       Date:  2008-06-07       Impact factor: 5.571

Review 9.  Evaluation of gastrointestinal drug supersaturation and precipitation: strategies and issues.

Authors:  Jan Bevernage; Joachim Brouwers; Marcus E Brewster; Patrick Augustijns
Journal:  Int J Pharm       Date:  2012-11-27       Impact factor: 5.875

10.  An investigation into the utility of a multi-compartmental, dynamic, system of the upper gastrointestinal tract to support formulation development and establish bioequivalence of poorly soluble drugs.

Authors:  Paul A Dickinson; Ragheb Abu Rmaileh; Lee Ashworth; Richard A Barker; Wendy M Burke; Claire M Patterson; Nick Stainforth; Mohammed Yasin
Journal:  AAPS J       Date:  2012-02-29       Impact factor: 4.009

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  2 in total

1.  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

2.  Approaches for Establishing Clinically Relevant Dissolution Specifications for Immediate Release Solid Oral Dosage Forms.

Authors:  Andre Hermans; Andreas M Abend; Filippos Kesisoglou; Talia Flanagan; Michael J Cohen; Dorys A Diaz; Y Mao; Limin Zhang; Gregory K Webster; Yiqing Lin; David A Hahn; Carrie A Coutant; Haiyan Grady
Journal:  AAPS J       Date:  2017-08-22       Impact factor: 4.009

  2 in total

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