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Clinical pharmacokinetic drug interactions associated with artemisinin derivatives and HIV-antivirals

机译:与青蒿素衍生物和艾滋病毒抗病毒相关的临床药代动力学药物相互作用

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摘要

Management of HIV and malaria co-infection is challenging due to potential drug-drug interactions between antimalarial and HIV-antiviral drugs. Little is known of the clinical significance of these drug interactions, and this review provides a comprehensive summary and critical evaluation of the literature. Specifically, drug interactions between WHO-recommended artemisinin combination therapies (ACT) and HIV-antivirals are discussed. An extensive literature search produced eight articles detailing n = 44 individual pharmacokinetic interactions. Only data pertaining to artemether-lumefantrine and two other artesunate combinations are available, but most of the interactions are characterized on at least two occasions by two different groups. Overall, protease inhibitors (PIs) tended to increase the exposure of lumefantrine and decrease the exposures of artemether and dihydroartemisinin, a pharmacologically active metabolite of artemether. Non-nucleoside reverse transcriptase inhibitors (NNRTIs) tended to decrease the exposures of artemether, dihydroartemisinin, and lumefantrine when co-administered with artemether-lumefantrine. Fewer studies characterized the effects of PIs or NNRTIs on artesunate combinations, but nevirapine increased artesunate exposure and ritonavir decreased dihydroartemisinin exposure. On the other hand, artemether-lumefantrine or artesunate combinations had little effect on the pharmacokinetics of HIV-antivirals, with the exception of decreased nevirapine exposure from artemether-lumefantrine or increased ritonavir exposure from pyronaridine/artesunate co-administration. In general, pharmacokinetic interactions can be explained by the metabolic properties of the co-administered drugs. Despite several limitations to the studies, these data do provide valuable insights into the potential pharmacokinetic perturbations, and the consistently marked elevation or reduction in ACT exposure in some cases cannot be overlooked.
机译:由于抗疟疾和艾滋病毒抗病毒药物之间的潜在药物 - 药物相互作用,艾滋病毒和疟疾的管理是挑战。众所周知,这些药物相互作用的临床意义,本综述提供了对文献的综合摘要和批判性评估。具体而言,讨论了谁推荐的青蒿素组合疗法(ACT)和艾滋病毒抗病患者之间的药物相互作用。广泛的文献搜索产生了八篇文章,详细介绍了n = 44个单独的药代动力学相互作用。只有与艺术品 - Lumefantrine和另外两种艺术组合有关的数据,但大多数相互作用的特征在于两次不同的组。总体而言,蛋白酶抑制剂(PIS)倾向于增加Lumefantrine的暴露并降低伪醚和二氢甲醛的曝光,一种药理上活性的蒿甲醇。非核苷逆转录酶抑制剂(NNRTIS)倾向于降低伪醚,二氢细胞蛋白和Lumefantrine的曝光,当与替摩尔醚 - Lumefantrine共同施用时。较少的研究表征了PIS或NNRTIS对艺术组合的影响,但Nevirapine增加了艺术暴露,Ritonavir降低了二氢血珠暴露。另一方面,Artemetret-Lumefantrine或artesunate组合对艾滋病毒抗病毒的药代动力学产生影响,除了来自蒿甲酰胺/艺术共同给药的丙啶rine或增加的ritonavir暴露而降低的Nevirapine暴露。通常,通过共同给药的药物的代谢性能可以解释药代动力学相互作用。尽管对研究有几个局限性,但这些数据确实为潜在的药代动力学扰动提供了有价值的见解,并且在某些情况下,行为暴露的始终标记的高度或减少不能被忽视。

著录项

  • 来源
    《Clinical pharmacokinetics》 |2014年第2期|共13页
  • 作者单位

    Faculty of Pharmaceutical Sciences University of British Columbia Vancouver BC Canada;

    College of Pharmacy Qatar University Doha Qatar;

    Faculty of Pharmaceutical Sciences University of British Columbia Vancouver BC Canada;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

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