A BIOLOGICALLY-BASED ALGORITHM FOR PREDICTING HUMAN TISSUE - BLOOD PARTITION COEFFICIENTS OF ORGANIC CHEMICALS

被引:87
作者
POULIN, P [1 ]
KRISHNAN, K [1 ]
机构
[1] UNIV MONTREAL,FAC MED,DEPT MED TRAVAIL & HYG MILIEU,MONTREAL,PQ H3C 3J7,CANADA
来源
HUMAN & EXPERIMENTAL TOXICOLOGY | 1995年 / 14卷 / 03期
关键词
PARTITION COEFFICIENTS; TISSUE; BLOOD PARTITIONING; PHYSIOLOGICALLY-BASED PHARMACOKINETIC MODELS;
D O I
10.1177/096032719501400307
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A biologically-based algorithm for predicting the tissue: blood partition coefficients (PCs) of organic chemicals has been developed. The approach consisted of (i) describing tissues and blood in terms of their neutral lipid, phospholipid, and water contents, (ii) obtaining data on the solubility of chemicals in n-octanol and water, and (iii) calculating the tissue: blood PCs by assuming that the solubility of a chemical in n-octanol corresponds to its solubility in neutral lipids, the solubility in water corresponds to the solubility in tissue/blood water fraction, and the solubility in phospholipids is a function of solubility in water and n-octanol. The adequacy of this approach was verified by comparing the predicted values with previously published experimental data on human tissue (liver, lung, muscle, kidney, brain, adipose tissue): blood PCs for 23 organic chemicals. In the case of liver, lung and muscle, the predicted PC values were in close agreement with the higher-end of the range of experimental PC values found in the literature. The predicted brain: and kidney: blood PCs were greater than the experimental PCs in most cases by approximately a factor of two. Whereas the adipose tissue: blood PCs of relatively less hydrophilic chemicals were adequately predicted, the predicted PCs for relatively more hydrophilic chemicals were much greater than the experimentally-determined values. There was a good agreement between the predicted and experimentally-determined blood solubility of the 23 chemicals chosen for this study, indicating that the over-estimation of tissue: blood PCs by the present method is not due to under-estimation of blood solubility of chemicals. Rather, it might be due to the lower tissue solubility of chemicals observed experimentally due to the complexity of the tissue matrices. This novel approach of describing tissues in terms of the type of lipid and water content should enable the prediction of the tissue: blood PCs of organic chemicals with information on their solubility in water and n-octanol, for developing physiologically-based toxicokinetic models.
引用
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页码:273 / 280
页数:8
相关论文
共 28 条
[1]   PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELING WITH DICHLOROMETHANE, ITS METABOLITE, CARBON-MONOXIDE, AND BLOOD CARBOXYHEMOGLOBIN IN RATS AND HUMANS [J].
ANDERSEN, ME ;
CLEWELL, HJ ;
GARGAS, ML ;
MACNAUGHTON, MG ;
REITZ, RH ;
NOLAN, RJ ;
MCKENNA, MJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 108 (01) :14-27
[2]  
[Anonymous], 1961, BIOCH HDB
[3]  
BOWEN DM, 1974, BIOCH LIPIDS, P141
[4]   ESTIMATION OF TISSUE-TO-PLASMA PARTITION-COEFFICIENTS USED IN PHYSIOLOGICAL PHARMACOKINETIC MODELS [J].
CHEN, HSG ;
GROSS, JF .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1979, 7 (01) :117-125
[5]   STRUCTURE AND QUANTIFICATION OF A PHYSIOLOGICAL MODEL OF THE DISTRIBUTION OF INJECTED AGENTS AND INHALED ANESTHETICS [J].
DAVIS, NR ;
MAPLESON, WW .
BRITISH JOURNAL OF ANAESTHESIA, 1981, 53 (04) :399-405
[6]  
FEINGOLD A, 1976, ANESTH ANALG, V55, P593
[7]  
FIESEROVABERGER.V, 1983, MODELING INHALATION, V1, P3
[8]  
FISEROVABERGERO.V, 1980, BRIT J IND MED, V37, P42
[9]  
FISEROVABERGERO.V, 1986, INT ARCH OCC ENV HEA, V58, P75
[10]   LIPIDS OF HUMAN MYOCARDIUM [J].
FLETCHER, RF .
LIPIDS, 1972, 7 (11) :728-&