首页> 外文期刊>Addiction biology >Effect of saquinavir/ritonavir (1000/100 mg bid) on the pharmacokinetics of methadone in opiate-dependent HIV-negative patients on stable methadone maintenance therapy.
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Effect of saquinavir/ritonavir (1000/100 mg bid) on the pharmacokinetics of methadone in opiate-dependent HIV-negative patients on stable methadone maintenance therapy.

机译:沙奎那韦/利托那韦(1000/100 mg bid)对稳定美沙酮维持治疗的阿片依赖性HIV阴性患者美沙酮药代动力学的影响。

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This study was performed to determine the effect of two protease inhibitors, saquinavir (SQV, oral 1000 mg bid) boosted by ritonavir (RTV, oral 100 mg bid), on pharmacokinetics (PK) of methadone in opiate-dependent HIV-negative patients on stable methadone maintenance therapy. This was a two-center, open-label, one-sequence cross-over, multiple-dose study in 13 HIV-negative patients who were on stable methadone therapy (oral, 60-120 mg qd). All patients continued methadone treatment on days 2-15. All patients received SQV/RTV in combination with methadone from days 2-15. PK of methadone was assessed on day 1 (alone) and on day 15 when methadone treatment was combined with SQV/RTV at steady state. Twelve patients completed the study. Median age, body weight and height were 50 years (range: 24-54 years), 80 kg (range: 57-97 kg) and 174 cm (range: 163-189 cm), respectively. All patients were Caucasian, and 11 were smokers. Median methadone dose was 85 mg qd. Geometric mean area under curve of the plasma concentration-time curve over 24 hour dosing interval (AUC(0-24 hour)) ratio of methadone with and without SQV/RTV was 0.81% (90% confidence interval: 71-91%). There was no significant plasma protein-binding displacement of methadone by SQV/RTV. The combination of SQV/RTV and methadone was well tolerated. There were no clinically significant adverse events or significant changes in laboratory parameters, electrocardiograms or vital signs. The 19% decrease in R-methadone AUC(0-24 hour) in the presence of SQV/RTV was not clinically relevant. There appears to be no need for methadone dose adjustment when methadone (60-120 mg qd) and SQV/RTV (1000/100 mg bid) are coadministered.
机译:进行这项研究的目的是为了确定两种蛋白酶抑制剂(沙奎那韦,SQV,口服1000 mg bid),由利托那韦(RTV,口服100 mg bid)增强,对阿片类药物依赖性HIV阴性患者美沙酮的药代动力学(PK)。稳定的美沙酮维持疗法。这是一项针对13名接受稳定美沙酮治疗(口服,每日60-120 mg)的HIV阴性患者的两中心,开放标签,单序列交叉,多剂量研究。所有患者在第2-15天继续接受美沙酮治疗。从第2-15天起,所有患者均接受SQ​​V / RTV联合美沙酮治疗。在稳定状态下,美沙酮治疗与SQV / RTV联合使用的第1天(单独)和第15天评估了美沙酮的PK。 12名患者完成了研究。中位年龄,体重和身高分别为50岁(范围:24-54岁),80公斤(范围:57-97公斤)和174厘米(范围:163-189厘米)。所有患者均为白种人,其中11人为吸烟者。美沙酮的中位剂量为每日85毫克。在有和没有SQV / RTV的美沙酮的24小时给药间隔(AUC(0-24小时))比率下,血浆浓度-时间曲线曲线下的几何平均面积为0.81%(90%置信区间:71-91%)。 SQV / RTV没有明显的美沙酮血浆蛋白结合置换作用。 SQV / RTV和美沙酮的组合耐受性良好。没有临床上的重大不良事件或实验室参数,心电图或生命体征的重大变化。在存在SQV / RTV的情况下,R-美沙酮AUC(0-24小时)下降19%与临床无关。当联合使用美沙酮(60-120 mg qd)和SQV / RTV(1000/100 mg bid)时,似乎无需调整美沙酮剂量。

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