A physiologically based pharmacokinetic computer model for human pregnancy.

A physiologically based pharmacokinetic (PBPK) model for human pregnancy must incorporate many factors that are not usually encountered in PBPK models of mature animals. Models for pregnancy must include the large changes that take place in the mother, the placenta and the embryo/fetus over the period of pregnancy. The embryo/fetal weight change was modeled using the Gompertz equation for growth which gave a good fit to extensive pooled weight data of the human embryo/fetus from 25 to 300 days of gestation. This equation is based on a growth rate that is proportional to the total weight of the organism with the proportionality factor decreasing exponentially with time. Allometric equations, which are widely used to relate organ weights, blood flow rates and other attributes of mature animals to total weight, were adapted to correlate fetal organ weights with total fetal weight. Allometric relationships were also developed for plasma flow rates and other organ-related parameters. The computer model, written in FORTRAN 77, included 27 compartments for the mother and 16 for the fetus; it also accommodates two substances allowing representation of a parent compound and a metabolite (or a second drug or environmental substance). Although this model is large, the inherent sparsity in the equations allow it to be solved numerically in a reasonable time on currently available, reasonably priced desktop computers. A nonlinear regression routine is included to fit key model parameters to experimental data. Concentrations of chemicals administered and measured in the mother may be simulated in both maternal and fetal organs at any day(s) between 25 days and 300 days of gestation. Allometric relationships are also utilized to adopt this human model for use with data obtained from animal experiments.

[1]  R. Pauli,et al.  Maternal and fetal sequelae of anticoagulation during pregnancy. , 1980, The American journal of medicine.

[2]  L. Zeise,et al.  Route-dependent pharmacokinetics, distribution, and placental permeability of organic and inorganic selenium in hamsters. , 1990, Teratology.

[3]  W. Wosilait 5 – Displacement Interactions Resulting from Competition for Binding Sites on Proteins , 1990 .

[4]  H J Clewell,et al.  Physiologically based pharmacokinetic modeling of the pregnant rat: a multiroute exposure model for trichloroethylene and its metabolite, trichloroacetic acid. , 1989, Toxicology and applied pharmacology.

[5]  J C Lewis,et al.  Microcomputer program for interactions in drug elimination in the rat. , 1988, Computer methods and programs in biomedicine.

[6]  W. S. Snyder,et al.  Report of the task group on reference man , 1979, Annals of the ICRP.

[7]  E. Adolph,et al.  Quantitative Relations in the Physiological Constitutions of Mammals. , 1949, Science.

[8]  R. Lutz,et al.  A preliminary pharmacokinetic model for several chlorinated biphenyls in the rat. , 1977, Drug metabolism and disposition: the biological fate of chemicals.

[9]  K. Bischoff,et al.  Methotrexate pharmacokinetics. , 1971, Journal of pharmaceutical sciences.

[10]  Mark A. Kramer,et al.  The simultaneous solution and sensitivity analysis of systems described by ordinary differential equations , 1988, TOMS.

[11]  A. K. Laird,et al.  Dynamics of relative growth. , 1965, Growth.

[12]  W. Slikker The role of metabolism in the testing of developmental toxicants. , 1987, Regulatory toxicology and pharmacology : RTP.

[13]  R. Luecke,et al.  Multifactorial modeling, drug interactions, liver damage and aging. , 1988, General pharmacology.

[14]  E J O'Flaherty,et al.  A physiologically based kinetic model of rat and mouse gestation: disposition of a weak acid. , 1992, Toxicology and applied pharmacology.

[15]  R. H. Luecke,et al.  Use Open Equations for Better Models , 1992 .

[16]  Benjamin Gompertz,et al.  XXIV. On the nature of the function expressive of the law of human mortality, and on a new mode of determining the value of life contingencies. In a letter to Francis Baily, Esq. F. R. S. &c , 1825, Philosophical Transactions of the Royal Society of London.

[17]  R K Jain,et al.  Physiologically based pharmacokinetic modeling: principles and applications. , 1983, Journal of pharmaceutical sciences.

[18]  J. Mordenti,et al.  Man versus beast: pharmacokinetic scaling in mammals. , 1986, Journal of pharmaceutical sciences.

[19]  Tyler Sa,et al.  Dynamics of normal growth. , 1965 .

[20]  R. Luecke,et al.  Physiological flow model for drug elimination interactions in the rat. , 1980, Computer Programs in Biomedicine.