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Influence of piperacillin on pharmacokinetics of etimicin in healthy volunteers

机译:哌拉西林对健康志愿者依替米星药代动力学的影响

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AIM: To investigate the influence of piperacillin on the pharmacokinetics of etimicin. METHODS: Ten healthy male volunteers subjects were administered randomly with 200 mg of etimicin alone or in combination with 2000 mg of piperacillin. After two weeks washout period, the subjects were crossed over to the second regimen. Blood and urinary samples were collected at specified time intervals. Etimicin concentration was analyzed using microbioassay method with Bacillus pumillus as the tested strain. Pharmacokinetic parameters were determined from serum concentration-time data with the 3p87-software package. RESULTS: Maximum serum concentrations of etimicin alone was (21 +- 5) mg/L compared with (19 +- 4) mg/L for the combination. The elimination half-lives were (1.9 +-0.4) h and (1.9 +- 0.2) h for etimicin alone and in combination, respectively. The area under the concentration-time curve of etimicin alone was (38 +- 7) mg·h·L~(-1) as opposed to (41 +- 8) mg·h·L~(-1) in combination. Twelve hours after administration, urinary recovery rates of etimicin were (56 +- 8) % and (56 +-6) % for etimicin alone and with piperacillin, respectively. CONCLUTION: The results indicated that the pharmacokinetics of etimicin was not affected by concurrent administration of piperacillin in healthy male volunteers. No modification in dosing regimen is necessary when two drugs were co-administered.
机译:目的:探讨哌拉西林对依替米星药代动力学的影响。方法:十名健康的男性志愿者受试者随机接受单独的200 mg依替米星或与2000 mg哌拉西林合用。在两周的冲洗期后,将受试者转移至第二方案。在指定的时间间隔收集血液和尿液样本。使用微生物测定法以枯草芽孢杆菌作为被测菌株分析了依替米星的浓度。使用3p87软件包根据血清浓度-时间数据确定药代动力学参数。结果:单独的依替米星的最大血清浓度为(21±5)mg / L,而联合用药的最高血清浓度为(19±4)mg / L。依替米星单独和组合的消除半衰期分别为(1.9±-0.4)h和(1.9±-0.2)h。单独的依替米星浓度-时间曲线下面积为(38 +-7)mg·h·L〜(-1),而组合时为(41 + -8)mg·h·L〜(-1)。给药十二小时后,单独使用依替米星和联合哌拉西林的依替米星的尿回收率分别为(56±8)%和(56 + -6)%。结论:在健康男性志愿者中,同时给予哌拉西林对依替米星的药代动力学没有影响。当同时使用两种药物时,无需修改给药方案。

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