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氟伏沙明对佐匹克隆药代动力学的影响:健康志愿者的两治疗期研究。

Effect of fluvoxamine on the pharmokinetics of zolpidem: a two-treatment period study in healthy volunteers.

机构信息

Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Pharmacy, University of Medicine and Pharmacy Iuliu Haţieganu, Cluj-Napoca, Romania.

出版信息

Clin Exp Pharmacol Physiol. 2012 Jan;39(1):9-12. doi: 10.1111/j.1440-1681.2011.05625.x.

Abstract
  1. Our objective was to evaluate a possible pharmacokinetic interaction between zolpidem and fluvoxamine in healthy volunteers. 2. The study consisted of two periods: Period 1 (reference), when each volunteer received a single dose of 5 mg zolpidem; and Period 2 (test), when each volunteer received a single dose of 5 mg zolpidem and 100 mg fluvoxamine. Between the two periods, the subjects were treated for 6 days with a single daily dose of 100 mg fluvoxamine. 3. Pharmacokinetic parameters of zolpidem given in each treatment period were calculated using non-compartmental analysis and the data from two periods were compared to determine statistically significant differences. 4. In the two periods of treatments, the mean peak plasma concentrations (C(max)) were 56.4 ± 25.6 ng/mL (zolpidem alone) and 67.3 ± 25.8 ng/mL (zolpidem after pretreatment with fluvoxamine). The t(max), times taken to reach C(max), were 0.83 ± 0.44 and 1.26 ± 0.74 h, respectively, and the total areas under the curve (AUC(0-∞)) were 200.9 ± 116.8 and 512.0 ± 354.6 ng h/mL, respectively. The half-life of zolpidem was 2.24 ± 0.81 h when given alone and 4.99 ± 2.92 h after pretreatment with fluvoxamine. 5. Fluvoxamine interacts with zolpidem in healthy volunteers and increases its exposure by approximately 150%. The experimental data showed the pharmacokinetic interaction between zolpidem and fluvoxamine, and suggest that the observed interaction might be clinically significant, but its relevance has to be confirmed.
摘要
  1. 我们的目的是评估健康志愿者中佐匹克隆和氟伏沙明之间可能存在的药代动力学相互作用。

  2. 该研究包括两个时期:第一期(参比期),每位志愿者接受单剂量 5 毫克佐匹克隆;第二期(试验期),每位志愿者接受单剂量 5 毫克佐匹克隆和 100 毫克氟伏沙明。在两个时期之间,受试者接受了 6 天的单剂量 100 毫克氟伏沙明治疗。

  3. 使用非房室分析计算每个治疗期给予的佐匹克隆的药代动力学参数,并比较两个时期的数据以确定是否存在统计学显著差异。

  4. 在两个治疗期,平均峰血浆浓度(C(max))分别为 56.4 ± 25.6 ng/mL(佐匹克隆单独使用)和 67.3 ± 25.8 ng/mL(佐匹克隆在氟伏沙明预处理后)。达到 C(max)的时间(t(max))分别为 0.83 ± 0.44 和 1.26 ± 0.74 h,曲线下面积(AUC(0-∞))分别为 200.9 ± 116.8 和 512.0 ± 354.6 ng h/mL。佐匹克隆的半衰期在单独使用时为 2.24 ± 0.81 h,在氟伏沙明预处理后为 4.99 ± 2.92 h。

  5. 氟伏沙明与健康志愿者中的佐匹克隆相互作用,使佐匹克隆的暴露量增加约 150%。实验数据显示了佐匹克隆和氟伏沙明之间的药代动力学相互作用,并表明观察到的相互作用可能具有临床意义,但需要确认其相关性。

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