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健康志愿者每日口服 300 毫克和 150 毫克拉米夫定后的拉米夫定及其三磷酸盐的药代动力学:ENCORE 2 研究结果。

Pharmacokinetics of lamivudine and lamivudine-triphosphate after administration of 300 milligrams and 150 milligrams once daily to healthy volunteers: results of the ENCORE 2 study.

机构信息

Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2012 Mar;56(3):1427-33. doi: 10.1128/AAC.05599-11. Epub 2011 Dec 19.

Abstract

There is interest in evaluating the efficacy of lower doses of certain antiretrovirals for clinical care. We determined here the bioequivalence of plasma lamivudine (3TC) and intracellular 3TC-triphosphate (3TC-TP) concentrations after the administration of two different doses. ENCORE 2 was a randomized crossover study. Subjects received 3TC at 300 and 150 mg once daily for 10 days (arm 1; n = 13) or vice versa (arm 2; n = 11), separated by a 10-day washout. Pharmacokinetic (PK) profiles (0 to 24 h) were assessed on days 10 and 30. Plasma 3TC and 3TC-TP levels in peripheral blood mononuclear cells were quantified by high-performance liquid chromatography-tandem mass spectrometry. Within-subject changes in PK parameters (the area under the concentration-time curve from 0 to 24 h [AUC(0-24)], the trough concentration of drug in plasma at 24 h [C(24)], and the maximum concentration of drug in plasma [C(max)]) were evaluated by determining the geometric mean ratios (GMRs) adjusted for study arm, period, and intra-individual variation. Regimens were considered bioequivalent if the 90% confidence interval (90% CI) fell within the range of 0.8 to 1.25. A total of 24 subjects completed the study. The GM (90% CI) 3TC AUC(0-24)), expressed as ng·h/ml, for the 300- and 150-mg doses were 8,354 (7,609 to 9,172) and 4,773 (4,408 to 5,169), respectively. Bioequivalence in 3TC PK following the administration of 300 and 150 mg was not demonstrated: the GMRs for AUC(0-24), C(24), and C(max) were 0.57 (0.55 to 0.60), 0.63 (0.59 to 0.67), and 0.56 (0.53 to 0.60), respectively. The GM (90% CI) 3TC-TP AUC(0-24) values (pmol·h/10(6) cells) for the 300- and 150-mg doses were 59.5 (51.8 to 68.3) and 44.0 (38.0 to 51.0), respectively. Bioequivalence in 3TC-TP PK following the administration of 300 and 150 mg was not demonstrated: the GMRs for AUC(0-24), C(24), and C(max) were 0.73 (0.64 to 0.83), 0.82 (0.68 to 0.99), and 0.70 (0.61 to 0.82), respectively. We found that 3TC at 150 mg is not bioequivalent to the standard regimen of 300 mg, indicating that saturation of cytosine phosphorylation pathways is not achieved at a dose of 150 mg.

摘要

人们对评估某些抗逆转录病毒的低剂量用于临床护理的疗效很感兴趣。我们在此确定了两种不同剂量给药后血浆拉米夫定(3TC)和细胞内 3TC-三磷酸(3TC-TP)浓度的生物等效性。ENCORE 2 是一项随机交叉研究。受试者每天接受 300mg 和 150mg 的 3TC 治疗,持续 10 天(第 1 组;n=13)或相反(第 2 组;n=11),两种剂量之间间隔 10 天洗脱期。在第 10 天和第 30 天评估了(0 至 24 小时)药代动力学(PK)曲线下面积(AUC(0-24))。通过高效液相色谱-串联质谱法定量外周血单核细胞中的血浆 3TC 和 3TC-TP 水平。通过确定研究臂、周期和个体内变异的几何平均比(GMR)来评估 PK 参数(从 0 到 24 小时的浓度-时间曲线下面积[AUC(0-24)]、24 小时时血浆中药物的谷浓度[C(24)]和血浆中药物的最大浓度[C(max)])的变化。如果 90%置信区间(90%CI)落在 0.8 至 1.25 范围内,则认为方案具有生物等效性。共有 24 名受试者完成了研究。300mg 和 150mg 剂量的 3TC AUC(0-24)的 GM(90%CI),表示为 ng·h/ml,分别为 8354(7609 至 9172)和 4773(4408 至 5169)。300mg 和 150mg 给药后 3TC PK 未显示生物等效性:AUC(0-24)、C(24)和 C(max)的 GMR 分别为 0.57(0.55 至 0.60)、0.63(0.59 至 0.67)和 0.56(0.53 至 0.60)。300mg 和 150mg 剂量的 3TC-TP AUC(0-24)GM(90%CI)值(pmol·h/106 细胞)分别为 59.5(51.8 至 68.3)和 44.0(38.0 至 51.0)。300mg 和 150mg 给药后 3TC-TP PK 也未显示生物等效性:AUC(0-24)、C(24)和 C(max)的 GMR 分别为 0.73(0.64 至 0.83)、0.82(0.68 至 0.99)和 0.70(0.61 至 0.82)。我们发现 150mg 的 3TC 与 300mg 的标准方案不具有生物等效性,这表明 150mg 剂量不能使胞嘧啶磷酸化途径饱和。

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