Hanna Julia, Foster David J R, Salter Amy, Somogyi Andrew A, White Jason M, Bochner Felix
Department of Clinical and Experimental Pharmacology, University of Adelaide, Adelaide, Australia.
Br J Clin Pharmacol. 2005 Oct;60(4):404-13. doi: 10.1111/j.1365-2125.2005.02464.x.
To investigate within- and between-subject variability of the pharmacodynamics and pharmacokinetics of (R)- and (S)-methadone in methadone maintenance subjects at steady-state.
Six non-holder subjects were studied on three occasions at 7-16 day intervals; doses (20-170 mg/day) remained unchanged. Blood samples and pharmacodynamic data were collected 10-12 times over a 24-h inter-dosing interval. All pharmacodynamic data were expressed as the area under the end-point versus time curve. Using analyses of variance with mixed effects, best estimates were made of the ratio of between- to within-subject variation, with corresponding 95% confidence intervals (CI) for within-subject variation at the average value.
Subjects were relatively consistent between occasions, whereas there was much greater between-subject variability (P < 0.02) for all measures. Estimates of the ratio of between- to within-subject variation ranged from 2.2-12.8 for pharmacodynamic measures, and 1.3-7.9 for pharmacokinetic parameters. For pain, total mood disturbance, withdrawal, pupil size and respiration rate, 95% CI for within-subject measures ranged < or = 2-fold, while this was greater for subjective direct opioid effects (4.2-fold). For CL/F of the active (R)-methadone, the variance ratio was 4.9 (P < 0.0003), with 95% CI for within-subject measures ranging < or = 2-fold. (S)-methadone CL/F demonstrated greater within-subject variability (3.4-fold), possibly contributing to a smaller (2.7; P < 0.0003) ratio of between- to within-subject variance.
Non-holder methadone maintenance treatment participants appear to respond consistently with respect to pharmacokinetics and pharmacodynamics over a 1-2 month period. Such knowledge may help prescribers to determine whether alternative dosing regimens or treatments might be more appropriate in this population.
研究美沙酮维持治疗患者在稳态时(R)-和(S)-美沙酮的药效学和药代动力学的个体内及个体间变异性。
对6名未戒断患者进行了3次研究,间隔7 - 16天;剂量(20 - 170毫克/天)保持不变。在给药间隔24小时内采集10 - 12次血样和药效学数据。所有药效学数据均表示为终点与时间曲线下的面积。使用混合效应方差分析,对个体间变异与个体内变异的比值进行最佳估计,并给出个体内变异在平均值时相应的95%置信区间(CI)。
患者在不同研究期间相对一致,然而所有测量指标的个体间变异性要大得多(P < 0.02)。个体间变异与个体内变异比值的估计值,药效学指标范围为2.2 - 12.8,药代动力学参数范围为1.3 - 7.9。对于疼痛、总体情绪障碍、戒断反应、瞳孔大小和呼吸频率,个体内测量的95%CI范围≤2倍,而主观直接阿片类效应则更大(4.2倍)。对于活性(R)-美沙酮的CL/F,方差比为4.9(P < 0.0003),个体内测量的95%CI范围≤2倍。(S)-美沙酮CL/F表现出更大的个体内变异性(3.4倍),这可能导致个体间与个体内方差的比值较小(2.7;P < 0.0003)。
未戒断的美沙酮维持治疗参与者在1 - 2个月期间的药代动力学和药效学反应似乎较为一致。这些知识可能有助于开处方者确定在该人群中替代给药方案或治疗方法是否更合适。