Drewelow Bernd, Schaffler Klaus, Reitmeir Peter, Bethke Thomas D
Institute of Clinical Pharmacology, University of Rostock, Rostock, Germany.
Arzneimittelforschung. 2010;60(8):483-91. doi: 10.1055/s-0031-1296316.
A randomized, double-blind, 2-way crossover trial of 24 healthy volunteers investigated the influence of esomeprazole (CAS 119141-88-7) and pantoprazole (CAS 102625-70-7), both 1 x 40 mg orally for 11 days, on the pharmacokinetics and pharmacodynamics of diazepam (CAS 439-14-5). Single-dose intravenous diazepam 0.1 mg/kg was administered on day 6. Blood sampling for pharmacokinetic assessment was conducted 0-120 h post diazepam application and data were analyzed using a model-independent approach and ANOVA. Pharmacodynamic parameters were assessed by an oculodynamic test and auditory evoked potentials 0-10 h post diazepam application. Data were analyzed using a linear mixed regression model. The AUC of diazepam was increased by 28.0%, Cmax by 31.4% and t1/2 by 41.1% in the esomeprazole vs. pantoprazole group. Myogenic parameters such as angular velocity of saccadic eye movements and complex choice reaction time were impaired with esomeprazole when compared to pantoprazole after diazepam administration (P < 0.0028) at 4-6 h. The sedation parameter microsleep doubled (2.6 vs. 1.1%; P < 0.0073). No differences in auditory evoked potentials were observed. In conclusion, it cannot be ruled out that a relevant pharmacodynamic interaction between diazepam and esomeprazole may occur when both drugs are concomitantly administered. Pantoprazole may provide a higher safety profile.
一项针对24名健康志愿者的随机、双盲、双向交叉试验,研究了埃索美拉唑(CAS 119141-88-7)和泮托拉唑(CAS 102625-70-7)(均口服1×40 mg,持续11天)对地西泮(CAS 439-14-5)药代动力学和药效学的影响。在第6天静脉注射单剂量地西泮0.1 mg/kg。在地西泮给药后0至120小时进行血样采集以进行药代动力学评估,并使用非模型依赖方法和方差分析对数据进行分析。在地西泮给药后0至10小时,通过眼动力学测试和听觉诱发电位评估药效学参数。使用线性混合回归模型对数据进行分析。与泮托拉唑组相比,埃索美拉唑组地西泮的AUC增加了28.0%,Cmax增加了31.4%,t1/2增加了41.1%。在给予地西泮后4至6小时,与泮托拉唑相比,埃索美拉唑使眼跳运动角速度和复杂选择反应时间等肌源性参数受损(P<0.0028)。镇静参数微睡眠增加了一倍(2.6%对1.1%;P<0.0073)。未观察到听觉诱发电位的差异。总之,不能排除地西泮和埃索美拉唑同时给药时可能发生相关药效学相互作用。泮托拉唑可能具有更高的安全性。