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Mechanistic ligand-receptor interaction model: operational model of agonism

机译:机械配体-受体相互作用模型:激动作用的操作模型

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摘要

This tutorial explains the basic principles of mechanistic ligand-receptor interaction model, which is an operational model of agonism. A growing number of agonist drugs, especially immune oncology drugs, is currently being developed. In this tutorial, time-dependent ordinary differential equation for simple operational model of agonism was derived step by step. The differential equation could be applied in a pharmacodynamic modeling software, such as NONMEM, for use in non-steady state experiments, in which experimental data are generated while the interaction between ligand and receptor changes over time. Making the most of the non-steady state experimental data would simplify the experimental processes, and furthermore allow us to identify more detailed kinetics of a potential drug. The operational model of agonism could be useful to predict the optimal dose for agonistic drugs from and animal pharmacology experiments at the very early phase of drug development.
机译:本教程说明了机械配体-受体相互作用模型的基本原理,这是一种激动作用的操作模型。目前正在开发越来越多的激动剂药物,尤其是免疫肿瘤药物。在本教程中,逐步推导了基于时间的常态微分方程,用于简单的激动作用模型。该微分方程可以应用于药效学建模软件,例如NONMEM,用于非稳态实验,在该实验中,当配体和受体之间的相互作用随时间变化时,生成实验数据。充分利用非稳态实验数据将简化实验过程,并且还使我们能够确定潜在药物的更详细动力学。激动作用的操作模型可用于在药物开发的早期阶段从动物药理实验和动物药理实验预测激动剂的最佳剂量。

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