Literature DB >> 15770643

Trends in solubility of polymorphs.

Madhu Pudipeddi1, Abu T M Serajuddin.   

Abstract

Polymorphism of drug substances has been the subject of intense investigation in the pharmaceutical field for over 40 years. Considering the multitude of reports on solubility or dissolution of polymorphs in the literature, an attempt is made in this study to answer the question: How big is the impact of polymorphism on solubility? A large number of literature reports on solubility or dissolution of polymorphs were reviewed and the data were analyzed for trends in solubility ratio of polymorphs. The general trend reveals that the ratio of polymorph solubility is typically less than 2, although occasionally higher ratios can be observed. A similar trend is also observed for anhydrate/hydrate solubility ratios, although anhydrate/hydrate solubility ratios appear to be more spread out and higher than the typical ratio for nonsolvated polymorphs. An attempt is also made in this commentary to estimate the ratio of solubilities of polymorphs from thermal data. The trend in estimated solubility ratio shows good agreement with the one observed with experimentally determined solubility values. Copyright 2005 Wiley-Liss, Inc

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Year:  2005        PMID: 15770643     DOI: 10.1002/jps.20302

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  27 in total

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2.  Discovery pharmaceutics--challenges and opportunities.

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Journal:  AAPS J       Date:  2006-06-02       Impact factor: 4.009

Review 3.  Recent progress in the computational prediction of aqueous solubility and absorption.

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Journal:  AAPS J       Date:  2006-02-03       Impact factor: 4.009

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Journal:  J Comput Aided Mol Des       Date:  2015-06-09       Impact factor: 3.686

5.  Crystalline form information from multiwell plate salt screening by use of Raman microscopy.

Authors:  Takashi Kojima; Satomi Onoue; Noriaki Murase; Fumie Katoh; Takashi Mano; Yoshihisa Matsuda
Journal:  Pharm Res       Date:  2006-04-06       Impact factor: 4.200

6.  Estimating the Aqueous Solubility of Pharmaceutical Hydrates.

Authors:  Stephen J Franklin; Usir S Younis; Paul B Myrdal
Journal:  J Pharm Sci       Date:  2016-06       Impact factor: 3.534

7.  Exploratory Study on Lercanidipine Hydrochloride Polymorphism: pH-Dependent Solubility Behavior and Simulation of its Impact on Pharmacokinetics.

Authors:  Ilia Alekseevich Repin; Raimar Loebenberg; John DiBella; António C L Conceição; Manuel E Minas da Piedade; Humberto G Ferraz; Michele G Issa; Nadia A Bou-Chacra; Catharine F M Ermida; Gabriel L B de Araujo
Journal:  AAPS PharmSciTech       Date:  2021-01-21       Impact factor: 3.246

8.  Toward the establishment of standardized in vitro tests for lipid-based formulations, part 3: understanding supersaturation versus precipitation potential during the in vitro digestion of type I, II, IIIA, IIIB and IV lipid-based formulations.

Authors:  Hywel D Williams; Philip Sassene; Karen Kleberg; Marilyn Calderone; Annabel Igonin; Eduardo Jule; Jan Vertommen; Ross Blundell; Hassan Benameur; Anette Müllertz; Colin W Pouton; Christopher J H Porter
Journal:  Pharm Res       Date:  2013-05-10       Impact factor: 4.200

9.  Improved pharmacokinetics of mercaptopurine afforded by a thermally robust hemihydrate.

Authors:  Kortney M Kersten; Adam J Matzger
Journal:  Chem Commun (Camb)       Date:  2016-03-22       Impact factor: 6.222

10.  Effect of polymer additives on the transformation of BMS-566394 anhydrate to the dihydrate form.

Authors:  S Betigeri; A Thakur; R Shukla; K Raghavan
Journal:  Pharm Res       Date:  2007-10-12       Impact factor: 4.200

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