Shiran Mohammad-Reza, Hosseinzadeh Rasa, Hamidikenari Abolhassan, Zarghami Mehran, Lamsehchi Nargess, Rafati Mohammad-Reza
Psychiatry and Behavioral Sciences Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Department of Pharmacotherapy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Iran J Psychiatry Behav Sci. 2011 Fall;5(2):53-61.
To investigate the pharmacokinetics (PK) and PK- pharmacodynamic (PD) relationship of methadone in a cohort of outpatients undergoing methadone maintenance treatment (MMT).
Sixty male patients undergoing MMT with a mean ±SD methadone daily dosage of 58 ± 34 mg were enrolled in this study. A 5-ml blood sample was collected before the daily intake of methadone. As a PD measure, the Subjective Opioid Withdrawal Scale (SOWS) form was completed immediately after obtaining the blood sample. Blood samples were taken and the forms were completed 4-5 times more (up to 24 hr) after the daily intake of methadone. Plasma methadone was analyzed using HPLC. Population PK/PD analysis was performed using population pharmacokinetics modeling software P-Pharm.
Significant decreases (p< 0.05) were observed in the SOWS scores during 10 hours after methadone intake. The SOWS had returned to baseline by 24 hr after using methaodone (p= 0.98). A considerable interindividual variability in the CL/F (16 fold), EC50 (3 fold) and Emax (6 fold) for methadone was observed.
Withdrawal symptoms were significantly improved in MMT patients after taking methadone and the PD measure was substantially affected by fluctuations in plasma methadone concentration. However, The SOWS had returned to baseline by 24 hr after using mathadone. Thus, a once daily dosing of methadone may not be suitable for those MMT patients who experience a significant withdrawal disturbance in the latter part of the interdose interval. This may increase the perceived severity of withdrawal and induce a craving for additional opioids.
研究美沙酮在一组接受美沙酮维持治疗(MMT)的门诊患者中的药代动力学(PK)及PK-药效学(PD)关系。
本研究纳入了60例接受MMT的男性患者,其美沙酮日均剂量平均为58±34mg。在每日服用美沙酮前采集5ml血样。作为药效学指标,在采集血样后立即填写主观阿片戒断量表(SOWS)。在每日服用美沙酮后,再采集血样并填写量表4-5次(最长至24小时)。采用高效液相色谱法分析血浆美沙酮。使用群体药代动力学建模软件P-Pharm进行群体PK/PD分析。
美沙酮摄入后10小时内,SOWS评分显著降低(p<0.05)。服用美沙酮24小时后,SOWS评分已恢复至基线水平(p=0.98)。观察到美沙酮的清除率/分布容积(CL/F)(16倍)、半数效应浓度(EC50)(3倍)和最大效应(Emax)(6倍)存在较大的个体间差异。
MMT患者服用美沙酮后戒断症状显著改善,且药效学指标受血浆美沙酮浓度波动的影响较大。然而,服用美沙酮24小时后SOWS评分已恢复至基线水平。因此,对于那些在给药间隔后期出现明显戒断不适的MMT患者,每日一次服用美沙酮可能并不合适。这可能会增加戒断的感知严重程度,并引发对额外阿片类药物的渴望。