Nia B, Vergnaud J M
Laboratory of Materials and Chemical Engineering, Faculty of Sciences, University of St-Etienne, France.
Eur J Drug Metab Pharmacokinet. 1996 Oct-Dec;21(4):333-8. doi: 10.1007/BF03189735.
The comparative pharmacokinetics of Aspegic, the lysine salt of acetylsalicylic acid, administered in multi doses either through i.v. or i.m. route was studied. 1 g of drug was injected each time with a frequency of 3 times a day. The pharmacokinetic parameters were determined using the experimental data in the literature. From these results, three categories of patients were considered, depending on their response to the drug. A numerical model was established in order to evaluate the following results: the drug level in the blood compartment obtained with the i.v. or i.m. administration, as well as the area under the curve for the first day and the third day when the so-called stationary state was obtained. Approximately similar values for AUC were obtained for each route of administration, for a given category of patients. The effect of the inter-variability of the patients characterised by their response to the drug was found to be of prime importance.
研究了通过静脉注射或肌肉注射多剂量给药的乙酰水杨酸赖氨酸盐阿斯匹林的比较药代动力学。每次注射1克药物,每天3次。使用文献中的实验数据确定药代动力学参数。根据这些结果,根据患者对药物的反应,将患者分为三类。建立了一个数值模型来评估以下结果:静脉注射或肌肉注射给药后血药浓度,以及在所谓稳态时第一天和第三天的曲线下面积。对于给定类别的患者,每种给药途径的曲线下面积值大致相似。发现患者对药物反应的个体差异的影响至关重要。