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孟鲁司特对健康志愿者华法林药代动力学和药效学的影响。

Effect of montelukast on the pharmacokinetics and pharmacodynamics of warfarin in healthy volunteers.

作者信息

Van Hecken A, Depré M, Verbesselt R, Wynants K, De Lepeleire I, Arnout J, Wong P H, Freeman A, Holland S, Gertz B, De Schepper P J

机构信息

Center for Clinical Pharmacology, UZ Gasthuisberg, KULeuven, Belgium.

出版信息

J Clin Pharmacol. 1999 May;39(5):495-500.

Abstract

Montelukast, a cysteinyl leukotriene receptor antagonist, is being developed for the treatment of asthma and related diseases. This study was designed to evaluate whether montelukast at clinically used dosage levels would interfere with the anticoagulant effect of warfarin. In a two-period, double-blind, randomized crossover study, 12 healthy male subjects received a single oral dose of 30 mg warfarin on the 7th day of a 12-day treatment with montelukast, 10 mg daily by mouth, or a placebo. Montelukast had no significant effect on the area under the plasma concentration-time curves and peak plasma concentrations of either R- or S-warfarin. However, slight but statistically significant decreases in time to peak concentration of both warfarin enantiomers and in elimination half-life of the less potent R-warfarin were observed in the presence of montelukast. These changes were not considered as clinically relevant. Montelukast had no significant effect on the anticoagulant effect of warfarin, as assessed by the international normalized ratio (INR) for prothrombin time (AUC0-144 and INR maximum). The results of this study suggest that a clinically important interaction between these drugs is unlikely to occur in patients requiring concomitant administration of both drugs.

摘要

孟鲁司特是一种半胱氨酰白三烯受体拮抗剂,目前正被开发用于治疗哮喘及相关疾病。本研究旨在评估临床使用剂量水平的孟鲁司特是否会干扰华法林的抗凝作用。在一项两阶段、双盲、随机交叉研究中,12名健康男性受试者在接受孟鲁司特(每日口服10 mg,共12天)或安慰剂治疗的第7天,单次口服30 mg华法林。孟鲁司特对R-或S-华法林的血浆浓度-时间曲线下面积及血浆峰浓度均无显著影响。然而,在使用孟鲁司特的情况下,观察到两种华法林对映体的达峰时间以及活性较低的R-华法林的消除半衰期均有轻微但具有统计学意义的降低。这些变化不被认为具有临床相关性。通过凝血酶原时间的国际标准化比值(INR)(AUC0-144和INR最大值)评估,孟鲁司特对华法林的抗凝作用无显著影响。本研究结果表明,在需要同时服用这两种药物的患者中,这两种药物之间不太可能发生具有临床重要意义的相互作用。

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