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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Pharmacokinetic Interaction between amprenavir and rifabutin or rifampin in healthy males.
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Pharmacokinetic Interaction between amprenavir and rifabutin or rifampin in healthy males.

机译:安普那韦与利福布汀或利福平在健康男性中的药代动力学相互作用。

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摘要

The objective of this study was to determine if there is a pharmacokinetic interaction when amprenavir is given with rifabutin or rifampin and to determine the effects of these drugs on the erythromycin breath test (ERMBT). Twenty-four healthy male subjects were randomized to one of two cohorts. All subjects received amprenavir (1,200 mg twice a day) for 4 days, followed by a 7-day washout period, followed by either rifabutin (300 mg once a day [QD]) (cohort 1) or rifampin (600 mg QD) (cohort 2) for 14 days. Cohort 1 then received amprenavir plus rifabutin for 10 days, and cohort 2 received amprenavir plus rifampin for 4 days. Serial plasma and urine samples for measurement of amprenavir, rifabutin, and rifampin and their 25-O-desacetyl metabolites, were measured by high-performance liquid chromatography. Rifabutin did not significantly affect amprenavir's pharmacokinetics. Amprenavir significantly increased the area under the curve at steady state (AUC(ss)) of rifabutin by 2.93-fold and the AUC(ss) of 25-O-desacetylrifabutin by 13.3-fold. Rifampin significantly decreased the AUC(ss) of amprenavir by 82%, but amprenavir had no effect on rifampin pharmacokinetics. Amprenavir decreased the results of the ERMBT by 83%. The results of the ERMBT after 2 weeks of rifabutin and rifampin therapy were increased 187 and 156%, respectively. Amprenavir plus rifampin was well tolerated. Amprenavir plus rifabutin was poorly tolerated, and 5 of 11 subjects discontinued therapy. Rifampin markedly increases the metabolic clearance of amprenavir, and coadministration is contraindicated. Amprenavir significantly decreases clearance of rifabutin and 25-O-desacetylrifabutin, and the combination is poorly tolerated. Amprenavir inhibits the ERMBT, and rifampin and rifabutin are equipotent inducers of the ERMBT.
机译:这项研究的目的是确定氨普那韦与利福布汀或利福平联用时是否存在药代动力学相互作用,并确定这些药物对红霉素呼气试验(ERMBT)的作用。 24名健康男性受试者被随机分为两个队列之一。所有受试者均接受安普那韦(1200毫克,每天两次),共4天,然后是7天的清除期,然后接受利福布汀(300毫克,每天一次[QD](组1)或利福平(600 mg QD)(第2组)进行14天。然后,队列1接受安普那韦加利福布汀治疗10天,队列2接受安普那韦加利福平治疗4天。通过高效液相色谱法测定了用于测定氨丙那韦,利福布汀和利福平及其25-O-去乙酰基代谢产物的系列血浆和尿液样品。利福布汀对氨普那韦的药代动力学没有明显影响。安普那韦显着增加了利福布汀稳态下曲线下面积(AUC(ss))2.93倍,而25-O-去乙酰基rifabutin的AUC(ss)增加了13.3倍。利福平显着降低了氨普那韦的AUC(ss)达82%,但氨普那韦对利福平的药代动力学没有影响。 Amprenavir使ERMBT的结果降低了83%。利福布汀和利福平治疗2周后的ERMBT结果分别增加187和156%。安普那韦加利福平耐受性良好。 Amprenavir加rifabutin的耐受性差,并且11名受试者中有5名停止了治疗。利福平显着增加了氨普那韦的代谢清除率,并且禁忌联合使用。安普那韦显着降低了利福布汀和25-O-去乙酰基利福布汀的清除率,并且该组合的耐受性差。 Amprenavir抑制ERMBT,而利福平和利福布汀是ERMBT的等价诱导剂。

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