体内药代动力学和药效学建模。

Critical reviews in bioengineering Pub Date : 1981-01-01
N H Holford, L B Sheiner
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引用次数: 0

摘要

描述和预测药物剂量与药效之间的关系是临床药理学的一个合理目标。涉及剂量-效应关系的过程可以分为两大类:药代动力学,涉及影响剂量-活性部位浓度过程的因素;药效学,描述活性部位浓度-效应过程。剂量效应关系模型的发展将从不区分药代动力学和药效学的剂量效应模型开始,发展到基于药代动力学预测活性位点浓度的模型,最后描述结合药代动力学和药效学模型来预测活性位点浓度和药物效应的模型。
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Pharmacokinetic and pharmacodynamic modeling in vivo.

A rational goal of clinical pharmacology is to described and predict the relationship between drug dose and drug effect. The processes involved in the dose-effect relationship can be described in two main categories - pharmacokinetics, which is concerned with factors affecting the dose-active site concentration process, and pharmacodynamics, which describes the active site concentration-effect process. The development of models of the dose-effect relationship will be described starting with dose-effect models which do not distinguish between pharmacokinetics and pharmacodynamics, progressing to models based upon pharmacokinetic predictions of the active site concentration, and finally describing models which combine both pharmacokinetic and pharmacodynamic models to predict both active site concentrations and the drug effect.

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