• 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

Bioavailability of ketoprofen in horses after rectal administration.

作者信息

Corveleyn S, Deprez P, Van der Weken G, Baeyens W, Remon J P

机构信息

Laboratory of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Universiteit Gent, Belgium.

出版信息

J Vet Pharmacol Ther. 1996 Oct;19(5):359-63. doi: 10.1111/j.1365-2885.1996.tb00064.x.

DOI:10.1111/j.1365-2885.1996.tb00064.x
PMID:8905569
Abstract

Six healthy mares ranging in age from 6 to 12 years and weighing from 415 to 540 kg were used to determine the rectal bioavailability of ketoprofen. For the rectal administration, three different formulations, each containing 1 g of ketoprofen, were administered in a fatty and a hydrophilic suppository base and as a liquid suspension. An average elimination half-life of 1.3 h (+/-1.2) was found. The average value for the total plasma clearance (ClT) was 131.9mL/ min.kg (range 95-183.5). The volume of distribution Vd(area) was 255 mL/kg and the mean residence time (MRT) value was 0.47 h. After rectal administration, the mean maximal plasma ketoprofen concentrations were 1.6(+/-0.8), 1.1(+/-0.7) and 1.6(+/-0.2) micrograms/mL for the fatty suppository, the hydrophilic suppository and the liquid suspension respectively. The absolute bioavailability of ketoprofen in horses after rectal administration of the three formulations was relatively low, with a large interindividual variability (24.5 +/- 9.5%, 28.7 +/- 18% and 31.3 +/- 6.8% for the fatty suppository, the hydrophilic suppository and the liquid suspension respectively). These values were not significantly different (P = 0.05; Friedman test). Despite the low rectal bioavailability obtained in this study, there was some evidence for the clinical effectiveness of the rectal formulations.

摘要

相似文献

1
Bioavailability of ketoprofen in horses after rectal administration.
J Vet Pharmacol Ther. 1996 Oct;19(5):359-63. doi: 10.1111/j.1365-2885.1996.tb00064.x.
2
Pharmacokinetics of intravenous and rectal ketoprofen in young children.幼儿静脉注射和直肠给药酮洛芬的药代动力学
Clin Pharmacokinet. 2003;42(4):373-9. doi: 10.2165/00003088-200342040-00005.
3
Bioavailability of racemic ketoprofen in healthy horses following rectal administration.消旋酮洛芬经直肠给药后在健康马匹中的生物利用度。
Res Vet Sci. 1999 Oct;67(2):203-4. doi: 10.1053/rvsc.1999.0303.
4
Influence of formulation on the pharmacokinetics and bioavailability of racemic ketoprofen in horses.制剂对马体内消旋酮洛芬药代动力学及生物利用度的影响。
J Vet Pharmacol Ther. 1995 Dec;18(6):446-50. doi: 10.1111/j.1365-2885.1995.tb00624.x.
5
Biopharmaceutical evaluation of ketoprofen following intravenous, oral, and rectal administration in dogs.酮洛芬在犬体内静脉注射、口服及直肠给药后的生物药剂学评价
J Pharm Sci. 1990 Jul;79(7):614-6. doi: 10.1002/jps.2600790715.
6
Ketoprofen suppository dosage forms: in vitro release and in vivo absorption studies in rabbits.酮洛芬栓剂剂型:家兔体内外释放及吸收研究
Drug Dev Ind Pharm. 1999 Feb;25(2):241-5. doi: 10.1081/ddc-100102166.
7
Pharmacokinetics and plasma concentrations of acetylsalicylic acid after intravenous, rectal, and intragastric administration to horses.乙酰水杨酸经静脉、直肠和胃内给药后在马体内的药代动力学及血浆浓度
Can J Vet Res. 2003 Oct;67(4):297-302.
8
Pharmacokinetics of ketoprofen in healthy foals less than twenty-four hours old.酮洛芬在出生不到24小时的健康幼驹体内的药代动力学。
Am J Vet Res. 1998 Mar;59(3):290-2.
9
Pharmacokinetics of carprofen enantiomers in equine plasma and synovial fluid - a comparison with ketoprofen.卡洛芬对映体在马血浆和滑液中的药代动力学——与酮洛芬的比较
J Vet Pharmacol Ther. 1999 Jun;22(3):196-201. doi: 10.1046/j.1365-2885.1999.00202.x.
10
In vitro-in vivo evaluation of in situ gelling and thermosensitive ketoprofen liquid suppositories.原位凝胶化热敏型酮洛芬液体栓剂的体外-体内评价
Eur J Drug Metab Pharmacokinet. 2014 Dec;39(4):283-91. doi: 10.1007/s13318-013-0157-6. Epub 2013 Oct 6.