Nikiforidis G C, Argyropoulos C P, Kassimatis T I, Ithakissios D S
Department of Medical Physics, School of Medicine, University of Patras, Greece.
Eur J Drug Metab Pharmacokinet. 1997 Jul-Sep;22(3):265-76. doi: 10.1007/BF03189817.
In the present paper, a nonlinear compartmental model for theophylline pharmacokinetics is developed. The analytical solution of the model, in parametric form, is derived under plateau conditions for plasma metabolite concentration. The parameters are obtained from plasma and urine data using best fitting techniques and their values are used in order to calculate maintenance intravenous infusion. Numerical simulation is then performed in order to compare the drug concentration obtained by our approach with that of alternative intravenous regimens. The differences argue for individualized dosage regimens, since theophylline is a drug with a narrow therapeutic window and its concentration at the active sites strongly depends on characteristic parameters of the patient's response. Our results show that it is possible to estimate the patients' parameters during the first 8 h after intravenous administration of the drug and these parameters can be used to design an individualized dosage regimen in patients receiving theophylline intravenously.
在本文中,开发了一种用于茶碱药代动力学的非线性房室模型。在血浆代谢物浓度的平台条件下,以参数形式推导了该模型的解析解。使用最佳拟合技术从血浆和尿液数据中获得参数,并使用其值来计算维持静脉输注量。然后进行数值模拟,以便将我们的方法获得的药物浓度与替代静脉给药方案的药物浓度进行比较。由于茶碱是一种治疗窗较窄的药物,其在活性部位的浓度强烈依赖于患者反应的特征参数,这些差异支持个体化给药方案。我们的结果表明,在静脉给药后的前8小时内可以估计患者的参数,并且这些参数可用于为接受静脉注射茶碱的患者设计个体化给药方案。