Physicochemical profiling in drug research: a brief survey of the state-of-the-art of experimental techniques

被引:119
作者
Avdeef, A
Testa, B [1 ]
机构
[1] Univ Lausanne, Inst Med Chem, Dept Pharm, CH-1015 Lausanne, Switzerland
[2] PION Inc, Woburn, MA 01801 USA
关键词
ionization; lipophilicity; distribution; solubility; permeability; screening; high-throughput method;
D O I
10.1007/PL00012496
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review begins with a general presentation of the new paradigm of drug discovery, with its emphasis on the rapid identification and elimination of compounds with unsuitable physicochemical and pharmacokinetic properties. The focus of the paper is on the various experimental methods used to determine such key physicochemical properties as ionization, lipophilicity and distribution in isotropic and anisotropic systems, solubility, and permeability across artificial membranes. Both traditional and high-throughput methods are presented and their limits highlighted. The text concludes with the trade-off between quantity/speed in high-throughput screening techniques versus greater data quality in the more labor-intensive methods.
引用
收藏
页码:1681 / 1689
页数:9
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