Quantitative structure-retention and retention-activity relationships of β-blocking agents by micellar liquid chromatography

被引:65
|
作者
Detroyer, A
Heyden, YV
Carda-Broch, S
García-Alvarez-Coque, MC
Massart, DL
机构
[1] Free Univ Brussels, Dept Pharmaceut & Biomed Anal, Inst Pharmaceut, B-1090 Brussels, Belgium
[2] Univ Valencia, Fac Quim, Dept Quim Analit, E-46100 Valencia, Spain
关键词
quantitative structure-retention relationship; quantitative retention-activity relationship; partition coefficient; beta-blockers;
D O I
10.1016/S0021-9673(01)00577-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sixteen beta -blocking agents (acebutolol, alprenolol, atenolol, bisoprolol, carteolol, celiprolol, esmolol, labetalol, metoprolol, nadolol, oxprenolol, pindolol. practolol, propranolol, sotalol and timolol) showing a large range of hydrophobicity (octanol-water partition coefficients, log P between -0.025 and 2.81) were subjected to micellar liquid chromatography with sodium dodecyl sulfate as micelle forming agent, and n-propanol as organic modifier. The correlation between log P and the retention factor extrapolated to a mobile phase free of micelles and organic modifier was investigated. The use of an interpolated retention factor or the retention factor for specific individual experimental mobile phases was however advantageous since the retention factors of all beta -blocking agents were measurable in the selected mobile phases. Good correlations with log P and with in vitro biological parameters (cellular permeability coefficients in Caco-2 monolayers and apparent permeability coefficients in rat intestinal segments) were found. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:211 / 221
页数:11
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