• 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

癫痫患者中美芬妥英及其代谢产物尼凡诺的处置情况。

Disposition of mephenytoin and its metabolite, nirvanol, in epileptic patients.

作者信息

Theodore W H, Newmark M E, Desai B T, Kupferberg H J, Penry J K, Porter R J, Yonekawa W D

出版信息

Neurology. 1984 Aug;34(8):1100-2. doi: 10.1212/wnl.34.8.1100.

DOI:10.1212/wnl.34.8.1100
PMID:6431315
Abstract

We investigated the conversion of mephenytoin to nirvanol in five patients with uncontrolled complex partial seizures. After a 50-mg single oral dose, mean peak mephenytoin level was 0.48 microgram/ml and nirvanol 0.37 microgram/ml. After 400 mg, peak mephenytoin level was 3.9 micrograms/ml and nirvanol 2.5 micrograms/ml. On 400 mg daily, mephenytoin reached a mean steady-state level of 1.5 micrograms/ml. Nirvanol mean steady-state level was 18 micrograms/ml. Mean plasma half-life was 17 hours for mephenytoin and 114 hours for nirvanol. Two patients had reduced seizures during mephenytoin therapy and one a transient increase during drug withdrawal. No toxicity was seen, but mephenytoin was not more effective than phenytoin.

摘要

我们研究了5例复杂部分性癫痫发作未得到控制的患者中,美芬妥因向尼凡诺的转化情况。单次口服50毫克后,美芬妥因的平均峰值水平为0.48微克/毫升,尼凡诺为0.37微克/毫升。服用400毫克后,美芬妥因的峰值水平为3.9微克/毫升,尼凡诺为2.5微克/毫升。每日服用400毫克时,美芬妥因的平均稳态水平为1.5微克/毫升。尼凡诺的平均稳态水平为18微克/毫升。美芬妥因的平均血浆半衰期为17小时,尼凡诺为114小时。两名患者在美芬妥因治疗期间癫痫发作减少,一名患者在停药期间短暂增加。未观察到毒性,但美芬妥因并不比苯妥英更有效。

相似文献

1
Disposition of mephenytoin and its metabolite, nirvanol, in epileptic patients.癫痫患者中美芬妥英及其代谢产物尼凡诺的处置情况。
Neurology. 1984 Aug;34(8):1100-2. doi: 10.1212/wnl.34.8.1100.
2
Mephenytoin: a reappraisal.美芬妥英:重新评估
Epilepsia. 1976 Dec;17(4):403-14. doi: 10.1111/j.1528-1157.1976.tb04452.x.
3
Pharmacokinetics of R-enantiomeric normephenytoin during chronic administration in epileptic patients.
Epilepsia. 1986 Jul-Aug;27(4):412-8. doi: 10.1111/j.1528-1157.1986.tb03560.x.
4
Relation of in vivo drug metabolism to stereoselective fetal hydantoin toxicology in mouse: evaluation of mephenytoin and its metabolite, nirvanol.
J Pharmacol Exp Ther. 1982 Apr;221(1):228-34.
5
Measurement of mephenytoin (3-methyl-5-ethyl-5-phenylhydantoin) and its demethylated metabolite by selective ion monitoring.
J Chromatogr. 1979 Jun 11;163(2):161-7. doi: 10.1016/s0378-4347(00)81459-0.
6
The metabolism of 3-methyl-5-ethyl-5-phenylhydantoin (mephenytoin) to 5-ethyl-5-phenylhydantoin (Nirvanol) in mice in relation to anticonvulsant activity.
Drug Metab Dispos. 1975 Jan-Feb;3(1):26-9.
7
Enantiospecific separation and quantitation of mephenytoin and its metabolites nirvanol and 4'-hydroxymephenytoin in human plasma and urine by liquid chromatography/tandem mass spectrometry.
Rapid Commun Mass Spectrom. 2006;20(3):463-72. doi: 10.1002/rcm.2324.
8
Increased systemic availability of drugs during acute ethanol intoxication: studies with mephenytoin in the dog.
J Pharmacol Exp Ther. 1980 Apr;213(1):173-8.
9
Clinical pharmacology of mephenytoin and ethotoin.
Ann Neurol. 1979 Nov;6(5):410-4. doi: 10.1002/ana.410060506.
10
Direct enantiomeric resolution of mephenytoin and its N-demethylated metabolite in plasma and blood using chiral capillary gas chromatography.
J Chromatogr. 1984 Apr 13;307(1):121-7. doi: 10.1016/s0378-4347(00)84078-5.

引用本文的文献

1
Formation of active metabolites of anticonvulsant drugs. A review of their pharmacokinetic and therapeutic significance.抗惊厥药物活性代谢物的形成。其药代动力学及治疗意义综述。
Clin Pharmacokinet. 1991 Jul;21(1):27-41. doi: 10.2165/00003088-199121010-00003.