High throughput solubility measurement in drug discovery and development

被引:305
作者
Alsenz, Jochem [1 ]
Kansy, Manfred [1 ]
机构
[1] F Hoffmann La Roche & Co Ltd, Div Pharma, Dept Preclin Res, CH-4070 Basel, Switzerland
关键词
solubility; kinetic solubility; thermodynamic (equilibrium) solubility; discovery; development; assay development; high throughput;
D O I
10.1016/j.addr.2007.05.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Measurement of drug solubility in various solvents is one of the key elements of compound characterization during the whole discovery and development process. This review summarizes current experimental approaches and addresses recent advances in the experimental methods used to determine drug solubility in drug discovery and early development. This paper focuses on high throughput methods designed to determine kinetic and thermodynamic (equilibrium) solubility but traditional methods are also presented. The focus, positioning, experimental setup, pros and cons, and limitations of individual assays are discussed and differences in solubility studies in discovery and development environments are highlighted. Finally, future needs and trends in solubility assay development designed to overcome current bottlenecks and trade-offs between speed and quality/quantity of measurements are addressed. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:546 / 567
页数:22
相关论文
共 158 条
[1]  
Alakhov V, 2001, Curr Opin Drug Discov Devel, V4, P493
[2]   Development of a partially automated solubility screening (PASS) assay for early drug development [J].
Alsenz, Jochem ;
Meister, Eva ;
Haenel, Elisabeth .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (07) :1748-1762
[3]   Relationship between Polysorbate 80 solubilization descriptors and octanol-water partition coefficients of drugs [J].
Alvarez-Núñez, FA ;
Yalkowsky, SH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 200 (02) :217-222
[4]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[5]   Physicochemical profiling in drug research: a brief survey of the state-of-the-art of experimental techniques [J].
Avdeef, A ;
Testa, B .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (10) :1681-1689
[6]   High-throughput measurements of solubility profiles [J].
Avdeef, A .
PHARMACOKINETIC OPTIMIZATION IN DRUG RESEARCH: BIOLOGICAL, PHYSICOCHEMICAL, AND COMPUTATIONAL STRATEGIES, 2001, :305-325
[7]   pH-metric solubility. 2: Correlation between the acid-base titration and the saturation shake-flask solubility-pH methods [J].
Avdeef, A ;
Berger, CM ;
Brownell, C .
PHARMACEUTICAL RESEARCH, 2000, 17 (01) :85-89
[8]   Solubility-excipient classification gradient maps [J].
Avdeef, Alex ;
Bendels, Stefanie ;
Tsinman, Oksana ;
Tsinman, Konstantin ;
Kansy, Manfred .
PHARMACEUTICAL RESEARCH, 2007, 24 (03) :530-545
[9]  
Avdeef Alex, 1998, Pharmacy and Pharmacology Communications, V4, P165
[10]   In silico approaches to prediction of aqueous and DMSO solubility of drug-like compounds:: Trends, problems and solutions [J].
Balakin, KV ;
Savchuk, NP ;
Tetko, IV .
CURRENT MEDICINAL CHEMISTRY, 2006, 13 (02) :223-241