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雷尼替丁与甲氧氯普胺的药代动力学相互作用研究。

Pharmacokinetic interaction study between ranitidine and metoclopramide.

作者信息

Leucuţa Adrian, Vlase Laurian, Farcău Dorin, Nanulescu Mircea

机构信息

3rd Pediatric Clinic, University of Medicine and Pharmacy, Str. Campeni 2-4, Cluj-Napoca, Romania.

出版信息

Rom J Gastroenterol. 2004 Sep;13(3):211-4.

Abstract

The pharmacokinetics of metoclopramide in healthy volunteers was evaluated to determine if previously repeated doses of ranitidine inhibit the metabolism of the gastrointestinal prokinetic drug. Metoclopramide 20 mg (tablets) in combination with ranitidine 150 mg (tablets) were administered to 14 healthy human volunteers in a two treatment study design, separated by 5 days in which the ranitidine alone was administrated in single p.o. doses twice daily. Plasma concentrations of metoclopramide were determined during a 24 hour period following drug administration. Metoclopramide plasma concentrations were determined by a validated RP-HPLC method. Pharmacokinetic parameters were calculated with compartmental and non-compartmental analysis. In the two periods of treatments, the mean peak plasma concentrations Cmax were 44 ng/ml (metoclopramide alone) and 49.2 ng/ml (metoclopramide and ranitidine). The time taken to reach the peak, Tmax, was 1.15 hrs, and 1.21 hrs, respectively. The total areas under the curve (AUC) was 314.3 ng.hr/ml and 354.06 ng.hr/ml, respectively. The half-life (T 1/2) was 5.6 hr and 6.7 hr. A statistically significant difference was observed for both AUC and half-life of metoclopramide when administered alone or after 5 days of treatment with ranitidine. The experimental data proved the pharmacokinetic interaction between ranitidine of metoclopramide, and suggest monitoring adverse effects in patients.

摘要

对健康志愿者中胃复安的药代动力学进行了评估,以确定先前重复给予雷尼替丁是否会抑制这种胃肠促动力药物的代谢。在一项双治疗研究设计中,将20毫克胃复安(片剂)与150毫克雷尼替丁(片剂)联合给予14名健康人类志愿者,两次治疗之间间隔5天,在此期间单独给予雷尼替丁,每日口服单剂量两次。在给药后的24小时内测定胃复安的血浆浓度。胃复安血浆浓度通过经过验证的反相高效液相色谱法测定。采用房室分析和非房室分析计算药代动力学参数。在两个治疗期,平均血浆峰浓度Cmax分别为44纳克/毫升(单独使用胃复安)和49.2纳克/毫升(胃复安和雷尼替丁)。达到峰值的时间Tmax分别为1.15小时和1.21小时。曲线下总面积(AUC)分别为314.3纳克·小时/毫升和354.06纳克·小时/毫升。半衰期(T 1/2)分别为5.6小时和6.7小时。单独给予胃复安或在给予雷尼替丁治疗5天后,胃复安的AUC和半衰期均观察到统计学上的显著差异。实验数据证明了雷尼替丁与胃复安之间的药代动力学相互作用,并建议对患者的不良反应进行监测。

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