Mahmood I, Sahlroot J T
Division of Pharmaceutical Evaluation I, Food and Drug Administration, Rockville, MD 20852, USA.
Biopharm Drug Dispos. 1997 Mar;18(2):117-26. doi: 10.1002/(sici)1099-081x(199703)18:2<117::aid-bdd5>3.0.co;2-c.
A limited sampling model has been developed for flunarizine following a 30 mg oral dose in epileptic patients who were receiving phenytoin or carbamazepine or both, to estimate the area under the curve (AUC) and maximum plasma concentration (Cmax). The model was developed using training data sets from 30, 20, 15, or 10 patients at one or two time points. The equations describing the models for AUC using two time points (3 and 24h) and Cmax for the training data set of 30 subjects were AUCpredicted = 11.1 C3h + 121.4 C24h - 157 (r = 0.80) Cmax(predicted) = 0.036 AUC + 42.9 (r = 0.74) The model was validated on 64 patients who received flunarizine orally. The model provided reasonably good estimates for both AUC and Cmax. The mean predicted AUC of flunarizine was 1230 +/- 717 ng h mL-1, whereas the observed AUC was 1203 +/- 900 ng h mL-1. The bias of the prediction was 2% and precision was 28%. The mean predicted Cmax of flunarizine was 86 +/- 32 ng mL-1 as compared to an observed mean Cmax of 90 +/- 42 ng mL-1. The bias and precision of the prediction were 4% and 24%, respectively. The method described here may be used to estimate AUC and Cmax for flunarizine without detailed pharmacokinetic studies.
已针对接受苯妥英或卡马西平或两者治疗的癫痫患者口服30 mg氟桂利嗪后,开发了一种有限采样模型,以估计曲线下面积(AUC)和最大血浆浓度(Cmax)。该模型是使用来自30、20、15或10名患者在一个或两个时间点的训练数据集开发的。描述使用两个时间点(3小时和24小时)的AUC模型以及30名受试者训练数据集的Cmax模型的方程为:AUC预测值 = 11.1×C3小时 + 121.4×C24小时 - 157(r = 0.80);Cmax(预测值) = 0.036×AUC + 42.9(r = 0.74)。该模型在64名口服氟桂利嗪的患者身上进行了验证。该模型对AUC和Cmax均提供了相当不错的估计。氟桂利嗪的平均预测AUC为1230±717 ng·h·mL-1,而观察到的AUC为1203±900 ng·h·mL-1。预测偏差为2%,精密度为28%。氟桂利嗪的平均预测Cmax为86±32 ng·mL-1,而观察到的平均Cmax为90±42 ng·mL-1。预测的偏差和精密度分别为4%和24%。此处描述的方法可用于在无需详细药代动力学研究的情况下估计氟桂利嗪的AUC和Cmax。