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对乙酰氨基酚和布洛芬与替米沙坦联合给药时在健康志愿者体内的药代动力学。

Pharmacokinetics of acetaminophen and ibuprofen when coadministered with telmisartan in healthy volunteers.

作者信息

Stangier J, Su C A, Fraunhofer A, Tetzloff W

机构信息

Department of Pharmacokinetics and Drug Metabolism, Boehringer Ingelheim Pharma KG, Birkendorfer Strasse, D-88397 Biberach an der Riss, Germany.

出版信息

J Clin Pharmacol. 2000 Dec;40(12 Pt 1):1338-46.

Abstract

Two open-label, two-way, crossover studies were performed to assess any pharmacokinetic interaction of telmisartan with either acetaminophen or ibuprofen. Healthy male adult volunteers (n = 12) received a single oral dose of acetaminophen 1 g alone and with oral telmisartan 120 mg in one study. Oral ibuprofen 400 mg three times daily with and without oral once-daily telmisartan 120 mg was given for 7 days in the other study conducted in 6 males and 6 females. In both studies, there was a washout period of > or = 13 days between single and combination medication administration. The primary end points Cmax and AUC were compared between combination (acetaminophen or ibuprofen + telmisartan) and single-agent medication (acetaminophen or ibuprofen). Pharmacokinetic drug interaction was assessed by analysis of variance (ANOVA) and calculation of 90% confidence intervals (CI) for treatment ratios using log-transformed parameters. Bioequivalence (i.e., lack of interaction) was concluded if the 90% CI of the ratios for both Cmax and AUC were within the acceptance limit of 0.80 to 1.25. Geometric mean Cmax values for acetaminophen and R-(-)- and S-(+)-ibuprofen enantiomers were similar with and without telmisartan coadministration (12.6 micrograms/mL vs. 14.1 micrograms/mL; 17.3 micrograms/mL vs. 16.7 micrograms/mL; 19.4 micrograms/mL vs. 19.5 micrograms/mL, respectively), and values for R-(-)- as well as S-(+)-ibuprofen were bioequivalent. Geometric mean AUC values for acetaminophen and R-(-)- and S-(+)-ibuprofen were also bioequivalent with and without telmisartan. The distribution and elimination parameters of both acetaminophen and ibuprofen were comparable in the presence or absence of telmisartan. The concomitant and single-agent medications were all well tolerated. In conclusion, the long half-life and excellent safety profile of telmisartan were unaffected by concurrent acetaminophen or ibuprofen medication; thus, once-daily dosing of telmisartan can be maintained, which may help to optimize patient compliance, and patients may self-administer concomitant acetaminophen or ibuprofen.

摘要

进行了两项开放标签、双向、交叉研究,以评估替米沙坦与对乙酰氨基酚或布洛芬之间的任何药代动力学相互作用。在一项研究中,12名健康成年男性志愿者单次口服1 g对乙酰氨基酚,同时口服120 mg替米沙坦。在另一项针对6名男性和6名女性的研究中,给予每日3次口服400 mg布洛芬,分别联合或不联合每日1次口服120 mg替米沙坦,持续7天。在两项研究中,单次用药和联合用药之间均有≥13天的洗脱期。比较联合用药(对乙酰氨基酚或布洛芬 + 替米沙坦)和单药治疗(对乙酰氨基酚或布洛芬)之间的主要终点Cmax和AUC。通过方差分析(ANOVA)和使用对数转换参数计算治疗比的90%置信区间(CI)来评估药代动力学药物相互作用。如果Cmax和AUC比值的90%CI在0.80至1.25的接受限度内,则得出生物等效性(即无相互作用)的结论。无论是否联用替米沙坦,对乙酰氨基酚以及R-(-)-和S-(+)-布洛芬对映体的几何平均Cmax值相似(分别为12.6μg/mL对14.1μg/mL;17.3μg/mL对16.7μg/mL;19.4μg/mL对19.5μg/mL),且R-(-)-和S-(+)-布洛芬的值具有生物等效性。无论是否使用替米沙坦,对乙酰氨基酚以及R-(-)-和S-(+)-布洛芬的几何平均AUC值也具有生物等效性。无论有无替米沙坦,对乙酰氨基酚和布洛芬的分布及消除参数均具有可比性。联合用药和单药治疗均耐受性良好。总之,替米沙坦的长半衰期和良好安全性不受同时使用对乙酰氨基酚或布洛芬的影响;因此,可以维持替米沙坦每日一次给药,这可能有助于优化患者依从性,且患者可自行服用对乙酰氨基酚或布洛芬。

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