Literature DB >> 12458685

Assuring quality and performance of sustained and controlled release parenterals: AAPS workshop report, co-sponsored by FDA and USP.

Diane J Burgess1, Ajaz S Hussain, Thomas S Ingallinera, Mei-Ling Chen.   

Abstract

This is a summary report of the American Association of Pharmaceutical Scientists, the Food and Drug Administration, and the United States Pharmacopoeia cosponsored workshop on "Assuring Quality and Performance of Sustained and Controlled Release Parenterals." Experts from the pharmaceutical industry, the regulatory authorities, and academia participated in this workshop to review, discuss, and debate formulation, processing, and manufacture of sustained and controlled release parenterals and identify critical process parameters and their control. Areas were identified where research is needed to understand the performance of these drug delivery systems and to assist in the development of appropriate testing procedures. Recommendations were made for future workshops, meetings, and working groups in this area.

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Year:  2002        PMID: 12458685     DOI: 10.1023/a:1020730102176

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


  11 in total

1.  Development of a dialysis in vitro release method for biodegradable microspheres.

Authors:  Susan S D'Souza; Patrick P DeLuca
Journal:  AAPS PharmSciTech       Date:  2005-10-06       Impact factor: 3.246

2.  Towards more realistic in vitro release measurement techniques for biodegradable microparticles.

Authors:  D Klose; N Azaroual; F Siepmann; G Vermeersch; J Siepmann
Journal:  Pharm Res       Date:  2008-10-29       Impact factor: 4.200

3.  Equivalence-by-design: targeting in vivo drug delivery profile.

Authors:  Mei-Ling Chen; Vincent H L Lee
Journal:  Pharm Res       Date:  2008-10-28       Impact factor: 4.200

4.  FIP/AAPS joint workshop report: dissolution/in vitro release testing of novel/special dosage forms.

Authors:  Cynthia K Brown; Horst Dieter Friedel; Amy R Barker; Lucinda F Buhse; Susanne Keitel; Todd L Cecil; Johannes Kraemer; J Michael Morris; Christos Reppas; Mary P Stickelmeyer; Chikako Yomota; Vinod P Shah
Journal:  AAPS PharmSciTech       Date:  2011-06-18       Impact factor: 3.246

5.  Macroporous acrylamide phantoms improve prediction of in vivo performance of in situ forming implants.

Authors:  Christopher Hernandez; Natalia Gawlik; Monika Goss; Haoyan Zhou; Selva Jeganathan; Danielle Gilbert; Agata A Exner
Journal:  J Control Release       Date:  2016-10-11       Impact factor: 9.776

6.  In vitro-in vivo correlation of parenteral risperidone polymeric microspheres.

Authors:  Jie Shen; Stephanie Choi; Wen Qu; Yan Wang; Diane J Burgess
Journal:  J Control Release       Date:  2015-09-28       Impact factor: 9.776

Review 7.  Accelerated in-vitro release testing methods for extended-release parenteral dosage forms.

Authors:  Jie Shen; Diane J Burgess
Journal:  J Pharm Pharmacol       Date:  2012-03-08       Impact factor: 3.765

8.  Formulation and evaluation of pharmaceutically equivalent parenteral depot suspension of methyl prednisolone acetate.

Authors:  A Alam; Alka Ahuja; Sanjula Baboota; S K Gidwani; J Ali
Journal:  Indian J Pharm Sci       Date:  2009-01       Impact factor: 0.975

Review 9.  Methods to assess in vitro drug release from injectable polymeric particulate systems.

Authors:  Susan S D'Souza; Patrick P DeLuca
Journal:  Pharm Res       Date:  2006-01-13       Impact factor: 4.580

10.  Effect of nonionic surfactants in release media on accelerated in-vitro release profile of sirolimus eluting stents with biodegradable polymeric coating.

Authors:  Ami Raval; Pratap Bahadur; Ankur Raval
Journal:  J Pharm Anal       Date:  2017-06-08
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