• 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

咖啡因、乙胺维林、保泰松、对乙酰氨基酚和苯巴比妥复方制剂片剂与栓剂的比较药代动力学研究(作者译)

[A comparative pharmacokinetic study for tablet and suppository formulations of a combination product of caffeine, ethaverine, propyphenazone, paracetamol and phenobarbital (author's transl)].

作者信息

Maier-Lenz H, Ringwelski L, Windorfer A

出版信息

Arzneimittelforschung. 1981;31(1):105-9.

PMID:7194086
Abstract

After the single-dose application of Migräne-Kranit, a combination of caffeine, ethaverine, propyphenazone, paracetamol and phenobarbital, tablets and suppositories in six healthy male volunteers aged from 24 to 28 years, serum concentrations were determined. The estimated relative bioavailabilities of the single substances in the suppository formulation vary between 120% for propyphenazone and 83% for phenobarbital in comparison to the tablets. The lag-times and the absorption rates for the substances in both formulations differ significantly. The absorption rates for the substances in the tablet are faster than for those in the suppository. The estimates for the elimination rates show only small differences between the two formulations.

摘要

在6名年龄在24至28岁的健康男性志愿者单次服用Migräne-Kranit(一种含有咖啡因、依沙维林、丙氧苯宗、对乙酰氨基酚和苯巴比妥的片剂和栓剂组合)后,测定了血清浓度。与片剂相比,栓剂制剂中单一物质的估计相对生物利用度在丙氧苯宗的120%至苯巴比妥的83%之间变化。两种制剂中这些物质的滞后时间和吸收速率有显著差异。片剂中物质的吸收速率比栓剂中的快。两种制剂的消除速率估计仅显示出微小差异。

相似文献

1
[A comparative pharmacokinetic study for tablet and suppository formulations of a combination product of caffeine, ethaverine, propyphenazone, paracetamol and phenobarbital (author's transl)].咖啡因、乙胺维林、保泰松、对乙酰氨基酚和苯巴比妥复方制剂片剂与栓剂的比较药代动力学研究(作者译)
Arzneimittelforschung. 1981;31(1):105-9.
2
[Comparative pharmacokinetics of paracetamol in humans following single oral and rectal administration (author's transl)].对乙酰氨基酚单次口服和直肠给药后在人体中的比较药代动力学(作者译)
Arzneimittelforschung. 1979;29(10):1607-11.
3
Bioavailability of two oral-tablet and two oral-suspension formulations of naproxen sodium/paracetamol (acetaminophen): single-dose, randomized, open-label, two-period crossover comparisons in healthy Mexican adult subjects.两种萘普生钠/对乙酰氨基酚口服片剂和两种口服混悬剂的生物利用度:在健康墨西哥成年受试者中进行的单剂量、随机、开放标签、两阶段交叉比较。
Clin Ther. 2009 Feb;31(2):399-410. doi: 10.1016/j.clinthera.2009.02.002.
4
[Relative bioavailability of paracetamol from tablets and suppositories as well as of paracetamol and codeine in a combination tablet].[对乙酰氨基酚片剂和栓剂以及复方片剂中对乙酰氨基酚与可待因的相对生物利用度]
Arzneimittelforschung. 1986 Mar;36(3):496-9.
5
[On the pharmacokinetics and bioavailability of paracetamol in suppositories for paediatry (author's transl)].对乙酰氨基酚儿科栓剂的药代动力学与生物利用度(作者译)
Arzneimittelforschung. 1982;32(4):420-2.
6
[Multiple-dose pharmacokinetics of paracetamol and salicylamide in man after combined rectal application (author's transl)].
Arzneimittelforschung. 1980;30(8):1295-8.
7
[The relative bioavailability of paracetamol in suppositories in comparison to tablets].对乙酰氨基酚栓剂与片剂相比的相对生物利用度
Arzneimittelforschung. 1996 Oct;46(10):975-80.
8
[Relative bioavailability of paracetamol in suppositories preparations in comparison to tablets].对乙酰氨基酚栓剂制剂与片剂相比的相对生物利用度
Arzneimittelforschung. 1994 Dec;44(12):1333-8.
9
Bioavailability of acetaminophen suppositories.对乙酰氨基酚栓剂的生物利用度。
Am J Hosp Pharm. 1975 Nov;32(11):1173-5.
10
[Comparative pharmacokinetics and relative bioavailability of the active principles diazepam, acetylsalicylic acid, caffeine, and dihydroergotamine tartrate in a combination product].[复方制剂中地西泮、乙酰水杨酸、咖啡因和酒石酸二氢麦角胺有效成分的比较药代动力学及相对生物利用度]
Arzneimittelforschung. 1982;32(3):289-93.

引用本文的文献

1
Analgesic effects of propyphenazone in comparison to its combination with caffeine.异丙安替比林及其与咖啡因组合的镇痛效果比较
Eur J Clin Pharmacol. 1996;49(5):377-82. doi: 10.1007/BF00203781.