Fleishaker J C, Peters G R
Clinical Pharmacokinetics Unit, Pharmacia & Upjohn, Inc., Kalamazoo, Michigan 49007, USA.
J Clin Pharmacol. 1996 Sep;36(9):809-13. doi: 10.1002/j.1552-4604.1996.tb04254.x.
The pharmacokinetics of tirilazad mesylate and its active reduced metabolite, U-89678, were evaluated in ischemic stroke patients receiving 2.5 mg/kg tirilazad every 3 hours for the first 12 hours of dosing followed by 2.5 mg/kg every 6 hours for a total of 22 doses (5 days). Trough and serial samples drawn during the 6 hours after administration of the last dose were analyzed for plasma levels of tirilazad and U-89678 by means of high-performance liquid chromatography. Complete concentration-time profiles were available for 20 patients, including 12 men (mean age, 68.0 years) and 8 women (mean age, 75.0 years). Trough concentrations of tirilazad and U-89678 were consistent with the loading regimen used. The mean area under the concentration-time curve from time 0 to 6 hours (AUC0-6) of tirilazad was 8181 +/- 2398 ng.hr/mL in men and 8135 +/- 3671 ng.hr/mL in women. The mean AUC0-6 of U-89678 was 2761 +/- 1834 ng.hr/mL in men and 1477 +/- 903 ng.hr/mL in women. These results show that gender has a modest effect on the pharmacokinetics of U-89678 but little effect on the pharmacokinetics of tirilazad in elderly ischemic stroke patients. These observations are consistent with previous findings in healthy young and elderly subjects.
在缺血性中风患者中评估了甲磺酸替拉扎特及其活性还原代谢产物U - 89678的药代动力学。给药的前12小时,每3小时给予患者2.5mg/kg甲磺酸替拉扎特,之后每6小时给予2.5mg/kg,共给药22次(5天)。在末次给药后6小时内采集谷值和系列样本,通过高效液相色谱法分析甲磺酸替拉扎特和U - 89678的血浆水平。获得了20例患者的完整浓度 - 时间曲线,其中包括12名男性(平均年龄68.0岁)和8名女性(平均年龄75.0岁)。甲磺酸替拉扎特和U - 89678的谷浓度与所用的负荷给药方案一致。男性甲磺酸替拉扎特从0至6小时的浓度 - 时间曲线下面积(AUC0 - 6)均值为8181±2398ng·hr/mL,女性为8135±3671ng·hr/mL。男性U - 89678的平均AUC0 - 6为2761±1834ng·hr/mL,女性为1477±903ng·hr/mL。这些结果表明,性别对老年缺血性中风患者U - 89678的药代动力学有一定影响,但对甲磺酸替拉扎特的药代动力学影响较小。这些观察结果与之前在健康年轻和老年受试者中的发现一致。