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清淡食物对三种苯二氮䓬类药物(夸西泮、硝西泮和地西泮)药代动力学和药效学的不同影响。

Different effects of light food on pharmacokinetics and pharmacodynamics of three benzodiazepines, quazepam, nitrazepam and diazepam.

作者信息

Yamazaki A, Kumagai Y, Fujita T, Hasunuma T, Yokota S, Maeda M, Otani Y, Majima M

机构信息

Department of Molecular Pharmacology, Kitasato University Graduate School of Medicinal graduate course, Kanagawa, Japan.

出版信息

J Clin Pharm Ther. 2007 Feb;32(1):31-9. doi: 10.1111/j.1365-2710.2007.00795.x.

Abstract

OBJECTIVE

Quazepam, nitrazepam and diazepam are administered under fed or fasted conditions for insomnia or anxiety disorder. Light bedtime food may have clinically relevant effects on the plasma levels of those drugs and hence on psychomotor performance. This study assessed the effect of light food on the pharmacokinetics and pharmacodynamics of these drugs.

METHOD

Twenty-one eligible subjects were randomized to one of three groups of seven subjects: quazepam 20 mg, diazepam 5 mg or nitrazepam 5 mg. Each healthy subject took a single oral dose of the assigned drug after overnight fasting and after light food, on a separate occasion. Blood samples were collected until 72 h after dosing. The plasma samples were assayed using high-pressure liquid chromatography with spectrophotometric detection. Reaction time, critical flicker fusion test and visual analogue scales were conducted.

RESULTS

The peak plasma concentration (C(max)) and area under the concentration-time curve (AUC) of quazepam with light food were 1.2-fold [90% confidence interval (CI): 1.1-1.5; P < 0.05] and 1.5-fold (90% CI: 1.3-1.9; P < 0.05) higher than that without light food, respectively. For nitrazepam and diazepam, the time to peak was delayed about 1 h in fed condition (P > 0.05). However it had no effect on their C(max) and AUC. Reaction time of quazepam with light food was prolonged at 4 and 6 h after dosing and its area under the effect-time curve from 0 to 10 h was increased (P < 0.05).

CONCLUSION

Light food increased the bioavailability of quazepam and affected psychomotor performance. Light food delayed T(max) of nitrazepam and diazepam but had no effect on C(max) and AUC.

摘要

目的

夸西泮、硝西泮和地西泮在进食或禁食条件下用于治疗失眠或焦虑症。睡前少量进食可能会对这些药物的血浆水平产生临床相关影响,进而影响精神运动表现。本研究评估了少量食物对这些药物药代动力学和药效学的影响。

方法

21名符合条件的受试者被随机分为三组,每组7人:分别服用20毫克夸西泮、5毫克地西泮或5毫克硝西泮。每位健康受试者在过夜禁食后和少量进食后,分别单次口服指定药物。给药后采集血样直至72小时。血浆样本采用带分光光度检测的高压液相色谱法进行测定。进行反应时间、临界闪烁融合试验和视觉模拟量表测试。

结果

进食少量食物时,夸西泮的血浆峰浓度(C(max))和浓度-时间曲线下面积(AUC)分别比未进食少量食物时高1.2倍[90%置信区间(CI):1.1 - 1.5;P < 0.05]和1.5倍(90% CI:1.3 - 1.9;P < 0.05)。对于硝西泮和地西泮,进食条件下达到峰浓度的时间延迟约1小时(P > 0.05)。然而,这对它们的C(max)和AUC没有影响。进食少量食物时,夸西泮给药后4小时和6小时的反应时间延长,其0至10小时效应-时间曲线下面积增加(P < 0.05)。

结论

少量食物增加了夸西泮的生物利用度并影响精神运动表现。少量食物延迟了硝西泮和地西泮的达峰时间(T(max)),但对C(max)和AUC没有影响。

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