Vachharajani N N, Shyu W C, Smith R A, Greene D S
Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb, Princeton, NJ 08043-4000, USA.
Br J Clin Pharmacol. 1998 Dec;46(6):611-3. doi: 10.1046/j.1365-2125.1998.00837.x.
Single dose pharmacokinetics and safety of irbesartan, an angiotensin II receptor antagonist, were evaluated in healthy young and elderly male and female subjects.
Irbesartan was administered as two 25 mg capsules after a 10 h fast to 12 young men, 12 young women, 12 elderly men and 12 elderly women. Serial blood and urine sample were collected up to 96 h after the dose. Plasma and urine samples were analysed for irbesartan by h.p.l.c./fluorescence methods.
No statistically significant gender effects were observed in peak plasma concentration (Cmax), area under the curve (AUC), and terminal elimination half-life (t1/2) of irbesartan. The geometric mean AUC and Cmax increased by about 43% and 49%, respectively, in the elderly subjects. Also the time to peak was significantly shorter in the elderly subjects compared with that observed in the young subjects. Renal clearance ofirbesartan was significantly reduced in the elderly females but this reduction is not likely to be of any clinical relevance since less than 3% of the administered dose of irbesartan is excreted unchanged in the urine.
Although there was an effect of age on the pharmacokinetics of irbesartan, based on the safety and efficacy profile, no adjustment in irbesartan dosage is necessary with respect to age or gender.
在健康青年和老年男性及女性受试者中评估血管紧张素II受体拮抗剂厄贝沙坦的单剂量药代动力学及安全性。
12名青年男性、12名青年女性、12名老年男性和12名老年女性在禁食10小时后服用两粒25毫克胶囊的厄贝沙坦。给药后长达96小时收集系列血液和尿液样本。采用高效液相色谱/荧光法分析血浆和尿液样本中的厄贝沙坦。
在厄贝沙坦的血浆峰浓度(Cmax)、曲线下面积(AUC)和终末消除半衰期(t1/2)方面未观察到具有统计学意义的性别效应。老年受试者的几何平均AUC和Cmax分别增加约43%和49%。此外,老年受试者达到峰浓度的时间明显短于青年受试者。老年女性中厄贝沙坦的肾清除率显著降低,但由于厄贝沙坦给药剂量中不到3%以原形经尿液排泄,这种降低不太可能具有任何临床相关性。
尽管年龄对厄贝沙坦的药代动力学有影响,但基于安全性和有效性概况,无需根据年龄或性别调整厄贝沙坦剂量。