摘要
在建立大鼠生理模型的基础上,模拟出了大鼠静脉注射环孢菌素A各主要器官或组织的时间-浓度曲线,并且与实验结果进行了对比,结果表明本方法具有一定的可行性.
Based on the general physiologically-based pharmcokinetics model of rat, the concentrations of cyclosporine A in blood and various organs or tissues in rat are simulated and these results are compared to those of experiments. This method is feasible.
出处
《西南民族大学学报(自然科学版)》
CAS
2005年第5期766-768,共3页
Journal of Southwest Minzu University(Natural Science Edition)
关键词
生理药物动力学模型
环孢菌素A
大鼠
数值模拟
general physiologically-based pharmcokinetics model
cyclosporine A
rat
simulation