Extension of the liquid chromatography/quantitative structure-property relationship method to assess the lipophilicity of neutral, acidic, basic and amphotheric drugs

被引:23
作者
Pallicer, Juan M. [1 ,2 ]
Calvet, Carme [3 ]
Port, Adriana [3 ]
Roses, Marti [1 ,2 ]
Rafols, Clara [1 ,2 ]
Bosch, Elisabeth [1 ,2 ]
机构
[1] Univ Barcelona, Dept Quim Analit, E-08028 Barcelona, Spain
[2] Univ Barcelona, Inst Biomed IBUB, E-08028 Barcelona, Spain
[3] ESTEVE, Barcelona 08041, Spain
关键词
Lipophilicity; Drugs; HPLC; UHPLC; QSPR model; Polarity model; WATER PARTITION-COEFFICIENTS; GRADIENT RP-HPLC; METRIC LOG-P; OF-THE-ART; MOBILE-PHASE; MULTIPROTIC SUBSTANCES; CHROMATOGRAPHIC METHOD; ARTIFICIAL MEMBRANE; POLARITY PARAMETER; ORGANIC-COMPOUNDS;
D O I
10.1016/j.chroma.2012.03.089
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A reported chromatographic method to determine the 1-octanol/water partition coefficient (log P-o/w) has been used to estimate the lipophilicity of 33 drugs with diverse structures and functionalities, including neutral, acid, basic, and amphoteric compounds. The applicability of the chromatographic method has been extended to the UHPLC technique, and the results obtained were compared to those obtained from conventional HPLC. No significant difference between the results obtained by both techniques is noticed. Thus, the suitability of UHPLC, which involves shorter run times, for lipophilicity assessment is demonstrated. In order to show the consistency of this chromatographic method, the log P-o/w, values of those drugs which have acid-base properties have been also determined by potentiometry, and the final results have been compared with both values derived from the chromatographic method and the ones from the literature. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 122
页数:10
相关论文
共 50 条
[1]  
Anderson S., COMMUNICATION
[2]   PH-METRIC LOG-P .1. DIFFERENCE PLOTS FOR DETERMINING ION-PAIR OCTANOL-WATER PARTITION-COEFFICIENTS OF MULTIPROTIC SUBSTANCES [J].
AVDEEF, A .
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 1992, 11 (04) :510-517
[3]   PH-METRIC LOG-P .2. REFINEMENT OF PARTITION-COEFFICIENTS AND IONIZATION-CONSTANTS OF MULTIPROTIC SUBSTANCES [J].
AVDEEF, A .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (02) :183-190
[4]   Fast determination of lipophilicity by HPLC [J].
Ayouni, L ;
Cazorla, G ;
Chaillou, D ;
Herbreteau, B ;
Rudaz, S ;
Lantéri, P ;
Carrupt, PA .
CHROMATOGRAPHIA, 2005, 62 (5-6) :251-255
[5]   Drug liposome partitioning as a tool for the prediction of human passive intestinal absorption [J].
Balon, K ;
Riebesehl, BU ;
Müller, BW .
PHARMACEUTICAL RESEARCH, 1999, 16 (06) :882-888
[6]   DIFFERENTIAL SCANNING CALORIMETRY STUDY OF THE INTERACTION OF ANTIDEPRESSANT DRUGS, NORADRENALINE, AND 5-HYDROXYTRYPTAMINE WITH A MEMBRANE MODEL [J].
BAUER, M ;
MEGRET, C ;
LAMURE, A ;
LACABANNE, C ;
FAURANCLAVEL, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (10) :897-901
[7]   REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY FOR EVALUATING THE LIPOPHILICITY OF PHARMACEUTICAL SUBSTANCES WITH IONIZATION UP TO LOG PAPP = 8 [J].
BELSNER, K ;
PFEIFER, M ;
WILFFERT, B .
JOURNAL OF CHROMATOGRAPHY, 1993, 629 (02) :123-134
[8]   Effect of n-octanol in the mobile phase on lipophilicity determination by reversed-phase high-performance liquid chromatography on a modified silica column [J].
Benhaim, Deborah ;
Grushka, Eli .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1209 (1-2) :111-119
[9]   LINEAR DESCRIPTION OF SOLUTE RETENTION IN REVERSED-PHASE LIQUID-CHROMATOGRAPHY BY A NEW MOBILE-PHASE POLARITY PARAMETER [J].
BOSCH, E ;
BOU, P ;
ROSES, M .
ANALYTICA CHIMICA ACTA, 1994, 299 (02) :219-229
[10]   A QSPR study of the p solute polarity parameter to estimate retention in HPLC [J].
Bosque, R ;
Sales, J ;
Bosch, E ;
Rosés, M ;
García-Alvarez-Coque, MC ;
Torres-Lapasió, JR .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2003, 43 (04) :1240-1247