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Grey-box pharmacokinetic/pharmacodynamic modelling of a euglycaemic clamp study

机译:血糖钳夹研究的灰色盒药代动力学/药效学建模

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摘要

Grey-box pharmacokinetic/pharmacodynamic (PK/PD) modelling is presented as a promising way of modelling the pharmacokinetics and pharmacodynamics of the in vivo system of insulin and glucose and to estimate model and derived PK/PD parameters. The concept behind grey-box modelling consists in using a priori physiological knowledge along with information from data in the estimation of model parameters. The PK/PD properties of two types of insulin are investigated in a euglycaemic clamp study where a single bolus of insulin is injected subcutaneously. The effect of insulin on the glucose disappearance is investigated by artificially maintaining a blood glucose concentration close to the normal fasting level. The infused glucose needed to maintain the clamped blood glucose concentration can therefore be used as a measure for the glucose utilization. The PK and PD parameters are successfully estimated simultaneously thereby describing the uptake, distribution, and effect of the two different types of insulin.
机译:Grey-box药代动力学/药效学(PK / PD)建模是为胰岛素和葡萄糖体内系统的药代动力学和药效学建模以及评估模型和推导的PK / PD参数的一种有前途的方法。灰箱建模背后的概念在于使用先验生理知识以及来自模型信息估计中的数据信息。在正常血糖钳位研究中研究了两种类型的胰岛素的PK / PD特性,在该研究中皮下注射了单剂量的胰岛素。通过人为地保持血糖浓度接近正常的禁食水平来研究胰岛素对葡萄糖消失的影响。因此,维持钳位血糖浓度所需的注入葡萄糖可以用作葡萄糖利用的量度。成功地同时估算了PK和PD参数,从而描述了两种不同类型胰岛素的吸收,分布和作用。

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