Literature DB >> 17055411

Solubility: it's not just for physical chemists.

Shobha N Bhattachar1, Laura A Deschenes, James A Wesley.   

Abstract

Solubility data are used to make crucial decisions from the earliest stages of drug discovery throughout the development process, but often the decision-maker is far removed, in terms of both organization and scientific background, from the scientist who generates the data. Here we provide a reference point for consumers of solubility who are presented with increasingly sophisticated strategies to measure sooner, faster or more accurately. We discuss the fundamental forces that govern solubility, the role of physical-chemical parameters such as pH and pK(a), and the principles involved in different solubility measurements. Our ultimate goal is to enable a decision-maker, when presented with solubility data, to have in hand the tools to evaluate not just the magnitude but also the context and appropriateness of those measurements to the drug in question.

Mesh:

Substances:

Year:  2006        PMID: 17055411     DOI: 10.1016/j.drudis.2006.09.002

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  13 in total

1.  Predicting the solubility of the anti-cancer agent docetaxel in small molecule excipients using computational methods.

Authors:  Loan Huynh; Justin Grant; Jean-Christophe Leroux; Pascal Delmas; Christine Allen
Journal:  Pharm Res       Date:  2007-08-18       Impact factor: 4.200

2.  Understanding the Differences Between Cocrystal and Salt Aqueous Solubilities.

Authors:  Katie L Cavanagh; Chinmay Maheshwari; Naír Rodríguez-Hornedo
Journal:  J Pharm Sci       Date:  2017-10-31       Impact factor: 3.534

Review 3.  Molecular photoswitches in aqueous environments.

Authors:  Jana Volarić; Wiktor Szymanski; Nadja A Simeth; Ben L Feringa
Journal:  Chem Soc Rev       Date:  2021-11-15       Impact factor: 54.564

4.  Rapid and efficient hydrophilicity tuning of p53/mdm2 antagonists.

Authors:  Stuti Srivastava; Barbara Beck; Wei Wang; Anna Czarna; Tad A Holak; Alexander Dömling
Journal:  J Comb Chem       Date:  2009 Jul-Aug

5.  Role of physiological intestinal water in oral absorption.

Authors:  Steven C Sutton
Journal:  AAPS J       Date:  2009-05-02       Impact factor: 4.009

6.  Influence of the solid form of siramesine hydrochloride on its behavior in aqueous environments.

Authors:  Anne Zimmermann; Fang Tian; Heidi Lopez de Diego; Michiel Ringkjøbing Elema; Jukka Rantanen; Anette Müllertz; Lars Hovgaard
Journal:  Pharm Res       Date:  2008-11-13       Impact factor: 4.200

7.  Investigation of the atypical glass transition and recrystallization behavior of amorphous prazosin salts.

Authors:  Lokesh Kumar; Dharmesh Popat; Arvind K Bansal
Journal:  Pharmaceutics       Date:  2011-08-25       Impact factor: 6.321

8.  Anti-Mycobacterial Evaluation of 7-Chloro-4-Aminoquinolines and Hologram Quantitative Structure-Activity Relationship (HQSAR) Modeling of Amino-Imino Tautomers.

Authors:  Marcelle L F Bispo; Camilo H S Lima; Laura N F Cardoso; André L P Candéa; Flávio A F M Bezerra; Maria C S Lourenço; Maria G M O Henriques; Ricardo B Alencastro; Carlos R Kaiser; Marcus V N Souza; Magaly G Albuquerque
Journal:  Pharmaceuticals (Basel)       Date:  2017-06-09

Review 9.  QSPR studies on aqueous solubilities of drug-like compounds.

Authors:  Pablo R Duchowicz; Eduardo A Castro
Journal:  Int J Mol Sci       Date:  2009-06-03       Impact factor: 6.208

10.  Influence of Solvent Composition on the Performance of Spray-Dried Co-Amorphous Formulations.

Authors:  Jaya Mishra; Thomas Rades; Korbinian Löbmann; Holger Grohganz
Journal:  Pharmaceutics       Date:  2018-04-12       Impact factor: 6.321

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.