Johnson S L, Mayersohn M
Biopharm Drug Dispos. 1985 Jul-Sep;6(3):313-23. doi: 10.1002/bdd.2510060306.
Plasma concentration-time data resulting from constant rate intravenous infusion may be analysed in two ways: Samples may be collected both during and after infusion and fit to an infusion model. Samples may be collected after infusion is complete and the data may be fit as an i.v. bolus. The purpose of this study was to contrast these two fitting procedures in terms of the accuracy of the parameter values obtained. Concentration-time data were computer-generated with the introduction of random error to simulate the disposition profiles of two model drugs. The results of these simulations indicate that satisfactory values for area-dependent parameters may be obtained without fitting data during the infusion phase. The exception to this is the apparent steady-state volume whose values become less accurate with longer infusion times. The parameters most affected by ignoring data points in the infusion phase are the central volume of distribution, and the coefficient and disposition rate constant associated with the initial, rapid phase of disposition. The equation which describes the entire concentration-time profile provides the most accurate parameter estimates of the model equation. In addition, we also describe the influence of the fitting method on the intercompartmental transfer rate constants.
恒速静脉输注产生的血浆浓度-时间数据可以通过两种方式进行分析:在输注期间和输注后均采集样本,并拟合输注模型。在输注完成后采集样本,数据可拟合为静脉推注。本研究的目的是对比这两种拟合程序在所得参数值准确性方面的差异。浓度-时间数据通过引入随机误差由计算机生成,以模拟两种模型药物的处置情况。这些模拟结果表明,在不拟合输注阶段数据的情况下,也可以获得与面积相关参数的满意值。明显的稳态容积是个例外,其值会随着输注时间的延长而变得不太准确。在输注阶段忽略数据点对参数影响最大的是中央分布容积,以及与初始快速处置阶段相关的系数和处置速率常数。描述整个浓度-时间曲线的方程可提供模型方程最准确的参数估计值。此外,我们还描述了拟合方法对隔室间转运速率常数的影响。