Luecke R H, Wosilait W D, Pearce B A, Young J F
Department of Chemical Engineering, University of Missouri-Columbia 65211.
Teratology. 1994 Feb;49(2):90-103. doi: 10.1002/tera.1420490205.
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.
用于人类妊娠的基于生理学的药代动力学(PBPK)模型必须纳入许多在成熟动物的PBPK模型中通常不会遇到的因素。妊娠模型必须包括在妊娠期间母亲、胎盘和胚胎/胎儿所发生的巨大变化。胚胎/胎儿体重变化采用Gompertz生长方程进行建模,该方程与妊娠25至300天大量汇总的人类胚胎/胎儿体重数据拟合良好。该方程基于与生物体总重量成比例的生长速率,比例因子随时间呈指数下降。广泛用于将成熟动物的器官重量、血流速率和其他属性与总重量相关联的异速生长方程,被用于将胎儿器官重量与胎儿总重量相关联。还建立了血浆流速和其他器官相关参数的异速生长关系。用FORTRAN 77编写的计算机模型包括母亲的27个隔室和胎儿的16个隔室;它还可容纳两种物质,能够表示母体化合物和代谢物(或第二种药物或环境物质)。尽管该模型规模较大,但方程中固有的稀疏性使其能够在当前可用的、价格合理的台式计算机上在合理时间内进行数值求解。包含一个非线性回归程序,用于将关键模型参数与实验数据拟合。在妊娠25天至300天之间的任何一天,可在母体和胎儿器官中模拟母亲体内给药和测量的化学物质浓度。异速生长关系也被用于将这个人类模型用于从动物实验获得的数据。