• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The influence of food on the disposition of the antiepileptic oxcarbazepine and its major metabolites in healthy volunteers.

作者信息

Degen P H, Flesch G, Cardot J M, Czendlik C, Dieterle W

机构信息

Ciba-Geigy Limited, Pharmaceuticals Division, Basel, Switzerland.

出版信息

Biopharm Drug Dispos. 1994 Aug;15(6):519-26. doi: 10.1002/bdd.2510150609.

DOI:10.1002/bdd.2510150609
PMID:7993989
Abstract

The effect of food on the pharmacokinetics of the antiepileptic oxcarbazepine (OXC) was investigated in healthy volunteers. Six healthy male volunteers were treated with single peroral doses of 600 mg of oxcarbazepine (Trileptal) after overnight fasting or a fat- and protein-rich breakfast. Mean (+/- SD) areas under the plasma concentration-time curves (AUC) of the major component in plasma, the active monohydroxy metabolite (MHD), which is responsible for the therapeutic effect in man, were 672 (25) mumol L-1 h when given to the fasted volunteers and 780 (31) mumol L-1 h (p = 0.042) when given after a substantial breakfast. Mean (+/- SD) maximum concentrations (Cmax) were 25.5 (4.8) mumol L-1 when given to the fasted volunteers and 31.4 (5.3) mumol L-1 (p = 0.025) when given after breakfast. Thus, the average AUC was increased by 16% and Cmax by 23% when oxcarbazepine was given with food. The times at which Cmax was reached (tmax) as well as the terminal half-lives were not influenced by concomitant intake of food. The tolerability was the same whether oxcarbazepine was given before or after food in healthy volunteers. The slight effect of food on the kinetics of oxcarbazepine should be of little therapeutic consequence.

摘要

相似文献

1
The influence of food on the disposition of the antiepileptic oxcarbazepine and its major metabolites in healthy volunteers.
Biopharm Drug Dispos. 1994 Aug;15(6):519-26. doi: 10.1002/bdd.2510150609.
2
Parent drug and/or metabolite? Which of them is most appropriate to establish bioequivalence of two oral oxcarbazepine formulations in healthy volunteers?母体药物和/或代谢物?在健康志愿者中,两者中哪一个最适合用于确定两种口服奥卡西平制剂的生物等效性?
Expert Opin Pharmacother. 2007 Jul;8(10):1415-23. doi: 10.1517/14656566.8.10.1415.
3
The influence of food on the disposition of the antiepileptic rufinamide in healthy volunteers.食物对健康志愿者中抗癫痫药物卢非酰胺处置的影响。
Biopharm Drug Dispos. 1998 May;19(4):259-62. doi: 10.1002/(sici)1099-081x(199805)19:4<259::aid-bdd98>3.0.co;2-v.
4
Influence of food on the disposition of the monoamine oxidase-A inhibitor brofaromine in healthy volunteers.
Biopharm Drug Dispos. 1993 Apr;14(3):209-15. doi: 10.1002/bdd.2510140304.
5
Pharmacokinetics of the monohydroxy derivative of oxcarbazepine and its enantiomers after a single intravenous dose given as racemate compared with a single oral dose of oxcarbazepine.奥卡西平单羟基代谢产物及其对映异构体在静脉注射给予外消旋体和口服奥卡西平单剂后的药代动力学比较。
Drug Metab Dispos. 2011 Jun;39(6):1103-10. doi: 10.1124/dmd.109.030593. Epub 2011 Mar 9.
6
Clinical pharmacokinetics of oxcarbazepine.奥卡西平的临床药代动力学
Clin Pharmacokinet. 2003;42(12):1023-42. doi: 10.2165/00003088-200342120-00002.
7
Assessment of the bioequivalence of two oxcarbazepine oral suspensions versus a film-coated tablet in healthy subjects.健康受试者中两种奥卡西平口服混悬液与薄膜包衣片的生物等效性评估。
Int J Clin Pharmacol Ther. 2003 Jul;41(7):299-308. doi: 10.5414/cpp41299.
8
Relative bioavailability, metabolism and tolerability of rectally administered oxcarbazepine suspension.直肠给药奥卡西平混悬液的相对生物利用度、代谢及耐受性
Clin Drug Investig. 2007;27(4):243-50. doi: 10.2165/00044011-200727040-00003.
9
Pharmacokinetics and tolerability of eslicarbazepine acetate and oxcarbazepine at steady state in healthy volunteers.在健康志愿者中,依托泊苷和依托泊苷葡甲胺稳态时的药代动力学和耐受性。
Epilepsia. 2013 Aug;54(8):1453-61. doi: 10.1111/epi.12242. Epub 2013 Jun 12.
10
Effects of charcoal on the absorption and elimination of the antiepileptic drugs lamotrigine and oxcarbazepine.活性炭对抗癫痫药物拉莫三嗪和奥卡西平吸收与消除的影响。
Arzneimittelforschung. 2010;60(7):421-6. doi: 10.1055/s-0031-1296306.

引用本文的文献

1
Application of Physiologically Based Pharmacokinetic Modeling to Predict Maternal Pharmacokinetics and Fetal Exposure to Oxcarbazepine.基于生理的药代动力学模型在预测母体奥卡西平药代动力学及胎儿暴露情况中的应用。
Pharmaceutics. 2022 Nov 3;14(11):2367. doi: 10.3390/pharmaceutics14112367.
2
Chronopharmacology of anti-convulsive therapy.抗惊厥治疗的时间药理学。
Curr Neurol Neurosci Rep. 2013 Apr;13(4):339. doi: 10.1007/s11910-013-0339-2.
3
Clinical pharmacokinetics of oxcarbazepine.奥卡西平的临床药代动力学
Clin Pharmacokinet. 2003;42(12):1023-42. doi: 10.2165/00003088-200342120-00002.
4
Oxcarbazepine: a review of its use in children with epilepsy.奥卡西平:用于癫痫患儿的综述。
Paediatr Drugs. 2003;5(8):557-73. doi: 10.2165/00148581-200305080-00006.
5
Food-drug interactions.食物-药物相互作用
Drugs. 2002;62(10):1481-502. doi: 10.2165/00003495-200262100-00005.
6
Oxcarbazepine: an update of its efficacy in the management of epilepsy.奥卡西平:其在癫痫治疗中疗效的最新进展
CNS Drugs. 2001;15(2):137-63. doi: 10.2165/00023210-200115020-00005.
7
Clinical pharmacokinetics of newer antiepileptic drugs. Lamotrigine, vigabatrin, gabapentin and oxcarbazepine.
Clin Pharmacokinet. 1996 Jun;30(6):403-15. doi: 10.2165/00003088-199630060-00001.