Lipophilicity and Its Relationship with Passive Drug Permeation

被引:341
作者
Liu, Xiangli [1 ]
Testa, Bernard [2 ]
Fahr, Alfred [1 ]
机构
[1] Univ Jena, Dept Pharmaceut Technol, D-07743 Jena, Germany
[2] CHUV BH04, Univ Hosp Ctr, Dept Pharm, CH-1011 Lausanne, Switzerland
关键词
lipophilicity; permeation; quantitative; structure-permeation relationships; LIPOSOME ELECTROKINETIC CHROMATOGRAPHY; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; WATER PARTITION-COEFFICIENTS; BLOOD-BRAIN-BARRIER; CAPILLARY ELECTROMIGRATION TECHNIQUES; PENETRANT STRUCTURE RELATIONSHIPS; IMMOBILIZED ARTIFICIAL MEMBRANES; CACO-2 CELL MONOLAYERS; SOLVENT SYSTEMS; STRATUM-CORNEUM;
D O I
10.1007/s11095-010-0303-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this review, we first summarize the structure and properties of biological membranes and the routes of passive drug transfer through physiological barriers. Lipophilicity is then introduced in terms of the intermolecular interactions it encodes. Finally, lipophilicity indices from isotropic solvent systems and from anisotropic membrane-like systems are discussed for their capacity to predict passive drug permeation across biological membranes such as the intestinal epithelium, the blood-brain barrier (BBB) or the skin. The broad evidence presented here shows that beyond the predictive power of lipophilicity parameters, the various intermolecular forces they encode allow a mechanistic interpretation of passive drug permeation.
引用
收藏
页码:962 / 977
页数:16
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