LogD:: Lipophilicity for ionisable compounds

被引:157
作者
Kah, Melanie [1 ]
Brown, Colin D. [2 ]
机构
[1] Cent Sci Lab, York YO41 1LZ, N Yorkshire, England
[2] Univ York, Dept Environm, York YO10 5DD, N Yorkshire, England
关键词
Kow; logP; hydrophobicity; pH; octanol-water; pow;
D O I
10.1016/j.chemosphere.2008.04.074
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The octanol/water partition coefficient (Kow) for organic compounds is widely used in predictive environmental studies. A significant proportion of contaminants of surface and ground water are ionisable (e.g. many pesticides, pharmaceuticals, metabolites). Such compounds may be partially ionised dependent on the pH. Since the neutral and ionic species exhibit different polarities, the Kow value of ionisable pesticides is pH dependent. It is therefore essential to determine Kow values over the full range of pH that occurs in the environment in order to get appropriate predictors. Numerous methods are available to measure lipophilicity but only a few are appropriate for ionisable pesticides (e.g. pH metric and filter probe methods). Parameters such as pH and ionic strength need to be carefully controlled when working with ionisable compounds. Variation of these factors probably explains why literature can yield Kow values that differ by more than one order of magnitude for some compounds. In this article, Kow values obtained for six acidic pesticides with three different methods are compared as well (data from the literature, measured by pH metric method and calculated with five computer programs). The values used in predictive regression equations needs to be either measured with a suitable method or selected from the literature with great care. Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1401 / 1408
页数:8
相关论文
共 61 条
[21]   ATOMIC PHYSICOCHEMICAL PARAMETERS FOR 3-DIMENSIONAL STRUCTURE DIRECTED QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS .3. MODELING HYDROPHOBIC INTERACTIONS [J].
GHOSE, AK ;
PRITCHETT, A ;
CRIPPEN, GM .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1988, 9 (01) :80-90
[22]   Octanol/water partitioning simulation by reversed-phase high performance liquid chromatography for structurally diverse acidic drugs:: Effect of n-octanol as mobile phase additive [J].
Giaginis, Costas ;
Theocharis, Stamatios ;
Tsantili-Kakoulidou, Anna .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1166 (1-2) :116-125
[23]   Screening of pesticides for environmental partitioning tendency [J].
Gramatica, P ;
Di Guardo, A .
CHEMOSPHERE, 2002, 47 (09) :947-956
[24]   Determination of octanol-water partition coefficient for terpenoids using reversed-phase high-performance liquid chromatography [J].
Griffin, S ;
Wyllie, SG ;
Markham, J .
JOURNAL OF CHROMATOGRAPHY A, 1999, 864 (02) :221-228
[25]   Prediction of the solubility, activity coefficient and liquid/liquid partition coefficient of organic compounds [J].
Hilal, SH ;
Karickhoff, SW ;
Carreira, LA .
QSAR & COMBINATORIAL SCIENCE, 2004, 23 (09) :709-720
[26]   Recent advances in computational prediction of drug absorption and permeability in drug discovery [J].
Hou, Tingjun ;
Wang, Junmei ;
Zhang, Wei ;
Wang, Wei ;
Xu, Xiaojie .
CURRENT MEDICINAL CHEMISTRY, 2006, 13 (22) :2653-2667
[27]   DISTRIBUTION OF HYDROPHOBIC IONOGENIC ORGANIC-COMPOUNDS BETWEEN OCTANOL AND WATER - ORGANIC-ACIDS [J].
JAFVERT, CT ;
WESTALL, JC ;
GRIEDER, E ;
SCHWARZENBACH, RP .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1990, 24 (12) :1795-1803
[28]   Prediction of the adsorption of ionizable pesticides in soils [J].
Kah, Melanie ;
Brown, Colin D. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (06) :2312-2322
[29]   APPARENT OCTANOL WATER PARTITION-COEFFICIENTS OF PENTACHLOROPHENOL AS A FUNCTION OF PH [J].
KAISER, KLE ;
VALDMANIS, I .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1982, 60 (16) :2104-2106
[30]   The E-state as an extended free valence [J].
Kier, LB ;
Hall, LH .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1997, 37 (03) :548-552