Defence Research and Development Canada-Toronto, Toronto, Ontario, Canada.
J Clin Pharmacol. 2013 Oct;53(10):1048-57. doi: 10.1002/jcph.131. Epub 2013 Jul 12.
Physiologically based pharmacokinetic models were developed using MATLAB Simulink® and PK-Sim®. We compared the capability and usefulness of these two models by simulating pharmacokinetic changes of midazolam under exercise and heat stress to verify the usefulness of MATLAB Simulink® as a generic PBPK modeling software. Although both models show good agreement with experimental data obtained under resting condition, their predictions of pharmacokinetics changes are less accurate in the stressful conditions. However, MATLAB Simulink® may be more flexible to include physiologically based processes such as oral absorption and simulate various stress parameters such as stress intensity, duration and timing of drug administration to improve model performance. Further work will be conducted to modify algorithms in our generic model developed using MATLAB Simulink® and to investigate pharmacokinetics under other physiological stress such as trauma.
我们使用 MATLAB Simulink® 和 PK-Sim® 开发了基于生理学的药代动力学模型。我们通过模拟咪达唑仑在运动和热应激下的药代动力学变化来比较这两种模型的能力和有用性,以验证 MATLAB Simulink® 作为通用 PBPK 建模软件的有用性。虽然这两种模型在休息状态下与实验数据都吻合良好,但在应激状态下,它们对药代动力学变化的预测准确性较低。然而,MATLAB Simulink® 可能更灵活,可以纳入基于生理学的过程,如口服吸收,并模拟各种应激参数,如应激强度、药物给药的持续时间和时间,以提高模型性能。我们将进一步修改使用 MATLAB Simulink® 开发的通用模型中的算法,并研究其他生理应激(如创伤)下的药代动力学。