Literature DB >> 12141269

Assuring quality and performance of sustained and controlled release parenterals: workshop report.

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 co-sponsored 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 in order 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: 12141269      PMCID: PMC2751292          DOI: 10.1208/ps040205

Source DB:  PubMed          Journal:  AAPS PharmSci        ISSN: 1522-1059


  16 in total

1.  FIP/AAPS guidelines to dissolution/in vitro release testing of novel/special dosage forms.

Authors:  Martin Siewert; Jennifer Dressman; Cynthia K Brown; Vinod P Shah
Journal:  AAPS PharmSciTech       Date:  2003       Impact factor: 3.246

2.  Assuring quality and performance of sustained and controlled release parenterals: EUFEPS workshop report.

Authors:  Diane J Burgess; Daan J A Crommelin; Ajaz S Hussain; Mei-Ling Chen
Journal:  AAPS PharmSci       Date:  2004-03-22

3.  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

4.  Accelerated in vitro release testing of implantable PLGA microsphere/PVA hydrogel composite coatings.

Authors:  Jie Shen; Diane J Burgess
Journal:  Int J Pharm       Date:  2011-10-13       Impact factor: 5.875

Review 5.  Critical factors influencing the in vivo performance of long-acting lipophilic solutions--impact on in vitro release method design.

Authors:  Susan Weng Larsen; Claus Larsen
Journal:  AAPS J       Date:  2009-11-06       Impact factor: 4.009

6.  A short term quality control tool for biodegradable microspheres.

Authors:  Susan D'Souza; Jabar A Faraj; Rossella Dorati; Patrick P DeLuca
Journal:  AAPS PharmSciTech       Date:  2014-02-12       Impact factor: 3.246

Review 7.  Role of In Vitro Release Methods in Liposomal Formulation Development: Challenges and Regulatory Perspective.

Authors:  Deepak Solomon; Nilesh Gupta; Nihal S Mulla; Snehal Shukla; Yadir A Guerrero; Vivek Gupta
Journal:  AAPS J       Date:  2017-09-18       Impact factor: 4.009

Review 8.  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

9.  Development and validation of a discriminative dissolution test for betamethasone sodium phosphate and betamethasone dipropionate intramuscular injectable suspension.

Authors:  Alice Simon; Vinícius Raphael de Almeida Borges; Lucio Mendes Cabral; Valéria Pereira de Sousa
Journal:  AAPS PharmSciTech       Date:  2013-02-01       Impact factor: 3.246

10.  Duel-acting subcutaneous microemulsion formulation for improved migraine treatment with zolmitriptan and diclofenac: formulation and in vitro-in vivo characterization.

Authors:  R Dubey; Luigi G Martini; Mark Christie
Journal:  AAPS J       Date:  2013-12-21       Impact factor: 4.009

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