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吡喹酮/青蒿琥酯与利托那韦在健康志愿者中的药物-药物相互作用分析。

Drug-drug interaction analysis of pyronaridine/artesunate and ritonavir in healthy volunteers.

出版信息

Am J Trop Med Hyg. 2012 Mar;86(3):489-495. doi: 10.4269/ajtmh.2012.11-0558.

Abstract

A multiple dose, parallel group study was conducted to assess for a drug-drug interaction between the pyronaridine/artesunate (PA) combination antimalarial and ritonavir. Thirty-four healthy adults were randomized (1:1) to receive PA for 3 days or PA with ritonavir (100 mg twice daily for 17 days, PA administered on Days 8-10). Pharmacokinetic parameters for pyronaridine, artesunate, and its active metabolite dihydroartemisinin (DHA) were obtained after the last PA dose and for ritonavir on Days 1 and 10. Ritonavir coadministration did not markedly change pyronaridine pharmacokinetics but resulted in a 27% increase in artesunate area under the curve (AUC) and a 38% decrease in DHA AUC. Ritonavir exposure was increased 3.2-fold in the presence of PA. The only relevant safety observations were increases in liver enzymes, only reaching a clinically significant grade in the PA + ritonavir arm. It was concluded that coadministered ritonavir and PA interact to alter exposure to artesunate, DHA, and ritonavir itself.

摘要

一项多剂量、平行组研究评估了吡喹酮/青蒿琥酯(PA)联合抗疟药物与利托那韦之间的药物相互作用。34 名健康成年人随机(1:1)接受 3 天的 PA 治疗或 PA 联合利托那韦(17 天,每日两次 100mg,PA 在第 8-10 天给药)。在最后一次 PA 给药后和第 1 天和第 10 天获得吡喹酮、青蒿琥酯及其活性代谢物二氢青蒿素(DHA)的药代动力学参数以及利托那韦的药代动力学参数。利托那韦联合给药并未显著改变吡喹酮的药代动力学参数,但导致青蒿琥酯 AUC 增加 27%,DHA AUC 减少 38%。在存在 PA 的情况下,利托那韦的暴露量增加了 3.2 倍。唯一相关的安全观察是肝酶升高,仅在 PA+利托那韦组达到临床显著水平。结论是,联合给予的利托那韦和 PA 相互作用,改变了青蒿琥酯、DHA 和利托那韦本身的暴露量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e81/3284369/9d2d1ec3ffa1/tropmed-86-489-g001.jpg

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