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多剂量利托那韦对利福布汀药代动力学的影响。

The effect of multiple doses of ritonavir on the pharmacokinetics of rifabutin.

作者信息

Cato A, Cavanaugh J, Shi H, Hsu A, Leonard J, Granneman R

机构信息

Pharmaceutical Products Division, Abbott Laboratories, Abbott Park, Ill., USA.

出版信息

Clin Pharmacol Ther. 1998 Apr;63(4):414-21. doi: 10.1016/S0009-9236(98)90036-4.

Abstract

OBJECTIVE

To investigate the effects of ritonavir on the pharmacokinetics of rifabutin.

METHODS

In a multiple-dose, randomized, parallel-group, double-blind study, subjects received 150 mg rifabutin daily for 24 days coadministered on days 15 to 24 with twice-daily doses of either placebo or ritonavir (300 mg on day 15, 400 mg on day 16, and 500 mg on days 17 to 24). Plasma concentrations of rifabutin and 25-O-desacetylrifabutin were measured by HPLC, and the pharmacokinetics were determined after the rifabutin doses on days 14 and 24.

RESULTS

For subjects receiving rifabutin and placebo who completed the study (n = 11), there were small but statistically significant differences (< or = 32%) in several rifabutin and 25-O-desacetylrifabutin pharmacokinetic parameters between the regimens of rifabutin alone and rifabutin with placebo. In contrast, the effect of ritonavir on rifabutin pharmacokinetics of subjects completing the study (n = 5) was substantial. Rifabutin mean minimum observed concentration (Cmin), maximum observed concentration (Cmax), and area under the concentration-time curve [AUC(0-24)] increased by approximately sixfold, 2.5-fold, and fourfold, respectively, and 25-O-desacetylrifabutin mean Cmin, Cmax, and AUC(0-24) increased by approximately 200-, 16-, and 35-fold, respectively, when coadministered with ritonavir compared with rifabutin administered alone. The sum of the mean AUC(0-24) of rifabutin and 25-O-desacetylrifabutin increased nearly sevenfold when coadministered with ritonavir.

CONCLUSIONS

Ritonavir inhibited the metabolism of rifabutin and 25-O-desacetylrifabutin, suggesting that both are metabolized at least in part by CYP3A. Ritonavir may have enhanced rifabutin bioavailability by reducing either intestinal of hepatic metabolism of both. Clarithromycin is an alternative to rifabutin for antimycobacterial therapy that may be administered concurrently with ritonavir. Administration of ritonavir with a reduced rifabutin dosage regimen (150 mg every Monday, Wednesday, and Friday) is being investigated.

摘要

目的

研究利托那韦对利福布汀药代动力学的影响。

方法

在一项多剂量、随机、平行组、双盲研究中,受试者每天服用150mg利福布汀,共24天,在第15至24天同时每日两次服用安慰剂或利托那韦(第15天300mg,第16天400mg,第17至24天500mg)。采用高效液相色谱法测定利福布汀和25 - O - 去乙酰利福布汀的血浆浓度,并在第14天和第24天服用利福布汀剂量后测定药代动力学。

结果

对于完成研究的接受利福布汀和安慰剂的受试者(n = 11),单独使用利福布汀方案与利福布汀加安慰剂方案之间,几种利福布汀和25 - O - 去乙酰利福布汀药代动力学参数存在微小但具有统计学意义的差异(≤32%)。相比之下,利托那韦对完成研究的受试者(n = 5)的利福布汀药代动力学影响显著。与单独服用利福布汀相比,与利托那韦合用时,利福布汀的平均最低观察浓度(Cmin)、最高观察浓度(Cmax)和浓度 - 时间曲线下面积[AUC(0 - 24)]分别增加了约6倍、2.5倍和4倍,25 - O - 去乙酰利福布汀的平均Cmin、Cmax和AUC(0 - 24)分别增加了约200倍、16倍和35倍。利福布汀和25 - O - 去乙酰利福布汀的平均AUC(0 - 24)之和与利托那韦合用时增加了近7倍。

结论

利托那韦抑制利福布汀和25 - O - 去乙酰利福布汀的代谢,表明两者至少部分通过CYP3A代谢。利托那韦可能通过减少两者在肠道或肝脏的代谢来提高利福布汀的生物利用度。克拉霉素是抗分枝杆菌治疗中利福布汀的替代药物,可与利托那韦同时使用。正在研究利托那韦与降低剂量的利福布汀给药方案(每周一、三、五服用150mg)联合使用的情况。

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