Literature DB >> 11170041

Comparison of chromatographic and spectroscopic methods used to rank compounds for aqueous solubility.

L Pan1, Q Ho, K Tsutsui, L Takahashi.   

Abstract

Rapid methods for ranking the solubility of compounds in aqueous media using commercial, 96-well ultraviolet-visible (UV-vis) and nephelometric plate readers are described. The methods were evaluated using commercially available compounds from a variety of structural classes as well as a series of structurally related compounds derived from combinatorial synthesis. Samples were predissolved in dimethyl sulfoxide (DMSO) and then added to the study solvent to attain a final concentration of DMSO in the aqueous solution of 5%. Comparison of filtration of the samples through nylon and poly(tetrafluoroethylene) (PTFE) membranes is also described. The solubility of the compounds determined using the UV-vis plate reader in the absorption mode (with samples filtered with the PTFE filter) as well as in the light scattering mode was in good agreement with that determined by high-performance liquid chromatography, with an average correlation of 0.95. Solubility data obtained using a 96-well nephelometer was also comparable (r(2) = 0.97). The nonequilibrium methods described in this study can be used to rapidly rank compounds from combinatorial libraries for solubility and can also give a general assessment of solubility prior to running additional high throughput screens in a drug discovery environment. Copyright 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:521-529, 2001

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Year:  2001        PMID: 11170041     DOI: 10.1002/1520-6017(200104)90:4<521::aid-jps1009>3.0.co;2-b

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


  7 in total

1.  Experimental and computational screening models for prediction of aqueous drug solubility.

Authors:  Christel A S Bergström; Ulf Norinder; Kristina Luthman; Per Artursson
Journal:  Pharm Res       Date:  2002-02       Impact factor: 4.200

2.  Solubility at the molecular level: development of a critical aggregation concentration (CAC) assay for estimating compound monomer solubility.

Authors:  Jie Wang; Edmund Matayoshi
Journal:  Pharm Res       Date:  2012-03-16       Impact factor: 4.200

3.  Impact of the amount of excess solids on apparent solubility.

Authors:  Kohsaku Kawakami; Kyoko Miyoshi; Yasuo Ida
Journal:  Pharm Res       Date:  2005-08-24       Impact factor: 4.200

4.  Challenges in the Conversion of Manual Processes to Machine-Assisted Syntheses: Activation of Thioglycoside Donors with Aryl(trifluoroethyl)iodonium Triflimide.

Authors:  Regis C Saliba; Zachary J Wooke; Gabriel A Nieves; An-Hsiang Adam Chu; Clay S Bennett; Nicola L B Pohl
Journal:  Org Lett       Date:  2018-01-16       Impact factor: 6.005

5.  Preparation of Glycyrrhetinic Acid Liposomes Using Lyophilization Monophase Solution Method: Preformulation, Optimization, and In Vitro Evaluation.

Authors:  Tingting Liu; Wenquan Zhu; Cuiyan Han; Xiaoyu Sui; Chang Liu; Xiaoxing Ma; Yan Dong
Journal:  Nanoscale Res Lett       Date:  2018-10-16       Impact factor: 4.703

6.  Harmonizing solubility measurement to lower inter-laboratory variance - progress of consortium of biopharmaceutical tools (CoBiTo) in Japan.

Authors:  Asami Ono; Naoya Matsumura; Takahiro Kimoto; Yoshiyuki Akiyama; Satoko Funaki; Naomi Tamura; Shun Hayashi; Yukiko Kojima; Masahiro Fushimi; Hiroshi Sudaki; Risa Aihara; Yuka Haruna; Maiko Jiko; Masaru Iwasaki; Takuya Fujita; Kiyohiko Sugano
Journal:  ADMET DMPK       Date:  2019-08-05

7.  Development of a Method for Fast Assessment of Protein Solubility Based on Ultrasonic Dispersion and Differential Centrifugation Technology.

Authors:  Dongwei Wei; Meng Wang; Hongdi Wang; Guijin Liu; Jun Fang; Yanbin Jiang
Journal:  ACS Omega       Date:  2022-08-22
  7 in total

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