• 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

人体口服埃托啡宁后的血浆水平。

Plasma levels of ethaverine after oral administration to humans.

作者信息

Meyer M C, Raghow G, Straughn A B

出版信息

Biopharm Drug Dispos. 1983 Oct-Dec;4(4):401-4. doi: 10.1002/bdd.2510040412.

DOI:10.1002/bdd.2510040412
PMID:6661518
Abstract

Fourteen healthy human subjects received a 200 mg oral dose of ethaverine hydrochloride as an elixir. Blood samples were obtained for 12 h after dosing. Plasma ethaverine concentrations were determined using a paired-ion, reversed-phase high performance liquid chromatographic method. Individual plasma concentration-time profiles were fitted to a two-compartment model with first-order absorption. The ethaverine was rapidly absorbed, based on a time of maximum plasma concentration of 0.75 h, a time-lag of 8.4 min, and an apparent first-order absorption half-life of 8.6 min. The mean terminal elimination half-life was 3.3 h.

摘要

14名健康受试者口服了200毫克盐酸乙苯福林酏剂。给药后12小时采集血样。采用离子对反相高效液相色谱法测定血浆中乙苯福林的浓度。将个体血浆浓度-时间曲线拟合为具有一级吸收的二室模型。根据血浆浓度达峰时间为0.75小时、时滞为8.4分钟以及表观一级吸收半衰期为8.6分钟,可知乙苯福林吸收迅速。平均终末消除半衰期为3.3小时。

相似文献

1
Plasma levels of ethaverine after oral administration to humans.人体口服埃托啡宁后的血浆水平。
Biopharm Drug Dispos. 1983 Oct-Dec;4(4):401-4. doi: 10.1002/bdd.2510040412.
2
Determination of the antispasmodic agent ethaverine in human plasma by high-performance liquid chromatography.
J Chromatogr. 1980 Jun 13;182(3-4):379-86. doi: 10.1016/s0378-4347(00)81487-5.
3
The influence of dosage form on papaverine bioavailability.剂型对罂粟碱生物利用度的影响。
J Clin Pharmacol. 1979 Aug-Sep;19(8-9 Pt 1):435-44. doi: 10.1002/j.1552-4604.1979.tb02505.x.
4
Inhibitory effects of ethaverine, a homologue of papaverine, on monoamine oxidase activity in mouse brain.罂粟碱同系物乙罂粟碱对小鼠脑内单胺氧化酶活性的抑制作用。
Biol Pharm Bull. 2001 Jul;24(7):838-40. doi: 10.1248/bpb.24.838.
5
Inhibitory effects of ethaverine, a homologue of papaverine, on dopamine content in PC12 cells.罂粟碱同系物乙凡林对PC12细胞中多巴胺含量的抑制作用。
Biol Pharm Bull. 2001 Jan;24(1):103-5. doi: 10.1248/bpb.24.103.
6
Pharmacology of ethaverine HC1: human and animal studies.
South Med J. 1975 Dec;68(12):1481-4. doi: 10.1097/00007611-197512000-00007.
7
Papaverine hydrochloride: the evaluation of two new dosage forms.盐酸罂粟碱:两种新剂型的评价
Int J Clin Pharmacol Biopharm. 1977 May;15(5):230-3.
8
Inhibition by ethaverine of catecholamine secretion through blocking L-type Ca2+ channels in PC12 cells.
Biochem Pharmacol. 1994 Mar 29;47(7):1262-6. doi: 10.1016/0006-2952(94)90399-9.
9
Effect of ethaverine hydrochloride on cochlear microcirculation.
Arch Otolaryngol. 1981 Apr;107(4):227-9. doi: 10.1001/archotol.1981.00790400029006.
10
Absolute and relative bioavailability of oral acetaminophen preparations.
J Pharm Sci. 1983 Aug;72(8):955-8. doi: 10.1002/jps.2600720832.