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Time effects of food intake on the pharmacokinetics and pharmacodynamics of quazepam.

机译:食物摄入量对Quzepam药代动力学和药效学的时间影响。

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AIMS: There is little information on interaction between food and the hypnotic agent quazepam. We therefore studied the effects of food and its time interval on the pharmacokinetics and pharmacodynamics of quazepam. METHODS: A randomized three-phase crossover study with 2-week intervals was conducted. Nine healthy male volunteers took a single oral 20 mg dose of quazepam under the following conditions: 1) after fasting overnight; 2) 30 min after eating standard meal; or 3) 3 h after eating the same meal. Plasma concentrations of quazepam and its metabolite, 2-oxoquazepam and psychomotor function using the Digit Symbol Substitute Test (DSST), Stanford Sleepiness Scale (SSS) and Visual Analogue Scale were measured up to 48 h. RESULTS: During the food treatments at 30 min and 3 h before dosing, the peak concentrations (Cmax) were 300% (95% CI 260, 340%; P < 0.001) and 250% (95% CI 210, 290%; P < 0.01) of the corresponding value during the fasting phase. For quazepam, the area under the plasma concentration-time curve from 0 to 8 h measured at 30 min and 3 h before dosing was significantly increased, with the food treatments by 2.4-fold (95% CI 2.0; 2.8-fold; P < 0.001) and 2.1-fold (95% CI 1.7; 2.4-fold; P < 0.01), respectively. In response to pharmacokinetic changes, some of the pharmacodynamics (DSST, P < 0.05; SSS, P < 0.05) differed significantly between fasted status and fed status. No difference was found in any pharmacokinetic or pharmacodynamic parameters between the two food treatment phases. CONCLUSIONS: A food effect on quazepam absorption is evident and continues at least until 3 h after food intake. The dosing of quazepam after a long period of ordinary fasting might reduce its efficacy because a 3 h interval between the timing of the evening meal and bedtime administration of hypnotics is regarded as normal in daily life.
机译:目的:关于食物与催眠药奎西p之间相互作用的信息很少。因此,我们研究了食物及其时间间隔对Quzepam药代动力学和药效学的影响。方法:进行了为期2周的随机三相交叉研究。九名健康的男性志愿者在以下情况下单次口服20毫克剂量的Quzepam:1)禁食过夜后; 2)吃标准餐后30分钟;或3)进餐后3小时。使用数字符号替代测试(DSST),斯坦福嗜睡量表(SSS)和视觉类比量表测量了quazepam及其代谢物,2-oxoquazepam和精神运动功能的血浆浓度,直至48小时。结果:在给药前30分钟和3小时的食物处理过程中,峰值浓度(Cmax)分别为300%(95%CI 260,340%; P <0.001)和250%(95%CI 210,290%; P <0.01)在禁食阶段的相应值。对于Quzepam,在给药前30分钟和3小时测量的0至8 h血浆浓度-时间曲线下的面积显着增加,其中食物处理增加了2.4倍(95%CI 2.0; 2.8倍; P < 0.001)和2.1倍(95%CI 1.7; 2.4倍; P <0.01)。响应药代动力学变化,禁食状态和进食状态之间的某些药效学(DSST,P <0.05; SSS,P <0.05)有显着差异。在两个食品处理阶段之间,在任何药代动力学或药效学参数方面均未发现差异。结论:食物对Quzepam吸收的作用是明显的,并且至少持续到食物摄入后3小时。长时间的常规禁食后服用奎西p可能会降低其疗效,因为在日常生活中,从晚餐时间到就寝时间服用催眠药之间的3小时间隔被认为是正常的。

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