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环孢菌素A的生理药物动力学模型 被引量:4

General physiologically pharmcokinetics model of cyclosporine A
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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
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