Literature DB >> 17084051

Current perspectives in dissolution testing of conventional and novel dosage forms.

Shirzad Azarmi1, Wilson Roa, Raimar Löbenberg.   

Abstract

The purpose of this article is to review USP and non-pharmacopeial dissolution testing methods for conventional and novel pharmaceutical dosage forms and give an insight to possible alternatives in drug dissolution study design and appropriate choices for dissolution media. For each dosage form first the USP method(s) for dissolution testing are reviewed followed by alternative methods used in research and development.

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Year:  2006        PMID: 17084051     DOI: 10.1016/j.ijpharm.2006.10.001

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  37 in total

1.  A semi-mechanistic modeling strategy to link in vitro and in vivo drug release for modified release formulations.

Authors:  Martin Bergstrand; Erik Söderlind; Ulf G Eriksson; Werner Weitschies; Mats O Karlsson
Journal:  Pharm Res       Date:  2011-09-27       Impact factor: 4.200

Review 2.  Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption.

Authors:  Joseph M Custodio; Chi-Yuan Wu; Leslie Z Benet
Journal:  Adv Drug Deliv Rev       Date:  2007-11-28       Impact factor: 15.470

3.  In vitro-in vivo correlation of efavirenz tablets using GastroPlus®.

Authors:  Thiago da Silva Honório; Eduardo Costa Pinto; Helvécio Vinicius A Rocha; Valeria Sant'Anna Dantas Esteves; Tereza Cristina dos Santos; Helena Carla Rangel Castro; Carlos Rangel Rodrigues; Valeria Pereira de Sousa; Lucio Mendes Cabral
Journal:  AAPS PharmSciTech       Date:  2013-08-14       Impact factor: 3.246

4.  Dissolution testing for generic drugs: an FDA perspective.

Authors:  Om Anand; Lawrence X Yu; Dale P Conner; Barbara M Davit
Journal:  AAPS J       Date:  2011-04-09       Impact factor: 4.009

5.  Dissolution testing of sublingual tablets: a novel in vitro method.

Authors:  Ousama Rachid; Mutasem Rawas-Qalaji; F Estelle R Simons; Keith J Simons
Journal:  AAPS PharmSciTech       Date:  2011-04-27       Impact factor: 3.246

6.  Linking dissolution to disintegration in immediate release tablets using image analysis and a population balance modelling approach.

Authors:  David Wilson; Stephen Wren; Gavin Reynolds
Journal:  Pharm Res       Date:  2011-08-11       Impact factor: 4.200

7.  Development and Validation of a Discriminatory Dissolution Model for an Immediately Release Dosage Form by DOE and Statistical Approaches.

Authors:  Mingkun Fu; Ellen Conroy; Michael Byers; Lakshminarasimhan Pranatharthiharan; Thierry Bilbault
Journal:  AAPS PharmSciTech       Date:  2021-04-21       Impact factor: 3.246

Review 8.  Application of UV Imaging in Formulation Development.

Authors:  Yu Sun; Jesper Østergaard
Journal:  Pharm Res       Date:  2016-10-20       Impact factor: 4.200

9.  Evolution of Choice of Solubility and Dissolution Media After Two Decades of Biopharmaceutical Classification System.

Authors:  Nadia Bou-Chacra; Katherine Jasmine Curo Melo; Ivan Andrés Cordova Morales; Erika S Stippler; Filippos Kesisoglou; Mehran Yazdanian; Raimar Löbenberg
Journal:  AAPS J       Date:  2017-05-17       Impact factor: 4.009

10.  Taste Masking of Griseofulvin and Caffeine Anhydrous Using Kleptose Linecaps DE17 by Hot Melt Extrusion.

Authors:  Abhishek Juluri; Carmen Popescu; Leon Zhou; Reena N Murthy; Vanaja K Gowda; P Chetan Kumar; Manjeet B Pimparade; Michael A Repka; S Narasimha Murthy
Journal:  AAPS PharmSciTech       Date:  2015-08-20       Impact factor: 3.246

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