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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HIV抗病毒药物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:由于抗疟药和HIV抗病毒药之间可能存在药物间相互作用,因此HIV和疟疾共感染的管理面临挑战。这些药物相互作用的临床意义鲜为人知,该综述提供了文献的全面总结和重要评价。具体而言,讨论了WHO推荐的青蒿素联合疗法(ACT)与HIV抗病毒药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。仅可获得有关蒿甲醚-荧光黄素和其他两种青蒿琥酯组合的数据,但大多数相互作用至少在两种情况下由两个不同的小组表征。总体而言,蛋白酶抑制剂(PIs)倾向于增加lumantantrine的暴露量并降低蒿甲醚和双氢青蒿素(蒿甲醚的药理活性代谢产物)的暴露。当与蒿甲醚-萤石黄碱共同施用时,非核苷逆转录酶抑制剂(NNRTIs)倾向于减少蒿甲醚,二氢青蒿素和麻黄素的暴露。较少的研究表征了PI或NNRTI对青蒿琥酯组合的影响,但是奈韦拉平增加了青蒿琥酯的暴露,利托那韦减少了双氢青蒿素的暴露。另一方面,蒿甲醚-氟美特林或青蒿琥酯组合对HIV-抗病毒药的药代动力学几乎没有影响,除了蒿甲醚-氟美特林对奈韦拉平的暴露减少或吡咯烷/青蒿琥酯共同给药对利托那韦的暴露增加。通常,药代动力学相互作用可以通过共同给药药物的代谢特性来解释。尽管研究存在一些局限性,但这些数据的确为潜在的药代动力学扰动提供了宝贵的见解,在某些情况下,ACT暴露的持续显着升高或降低也不能忽略。

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