Suppr超能文献

氟苯尼考对牛静脉注射和肌肉注射后的药代动力学

Pharmacokinetics of florfenicol following intravenous and intramuscular doses to cattle.

作者信息

Lobell R D, Varma K J, Johnson J C, Sams R A, Gerken D F, Ashcraft S M

机构信息

Schering-Plough Corporation, Cranford, New Jersey.

出版信息

J Vet Pharmacol Ther. 1994 Aug;17(4):253-8. doi: 10.1111/j.1365-2885.1994.tb00241.x.

Abstract

The disposition of florfenicol after single intravenous and intramuscular doses of 20 mg of florfenicol/kg of body weight (b.w.) to feeder calves was investigated. Serum florfenicol concentrations were determined by a sensitive high performance liquid chromatographic method with a limit of quantitation of 0.025 microgram/ml. The extent of serum protein binding of florfenicol was only 13.2% at a serum florfenicol concentration of 3.0 micrograms/ml. Serum concentration-time data after intravenous administration were best described by a triexponential equation. Total body clearance and steady state volume of distribution were 3.75 ml/min/kg b.w. and 761 ml/kg b.w., respectively. The terminal half-life after intravenous administration was 159 min. The absolute systemic availability after intramuscular administration was 78.5% (range: 59.3-106%) and the harmonic mean of the terminal half-life was 1098 minutes, indicating slow release of the florfenicol from the formulation at the intramuscular injection site.

摘要

研究了给育肥牛单次静脉注射和肌肉注射20毫克氟苯尼考/千克体重后的氟苯尼考处置情况。采用灵敏的高效液相色谱法测定血清氟苯尼考浓度,定量限为0.025微克/毫升。在血清氟苯尼考浓度为3.0微克/毫升时,氟苯尼考的血清蛋白结合率仅为13.2%。静脉给药后的血清浓度-时间数据用三指数方程描述最佳。总体清除率和稳态分布容积分别为3.75毫升/分钟/千克体重和761毫升/千克体重。静脉给药后的终末半衰期为159分钟。肌肉注射后的绝对全身生物利用度为78.5%(范围:59.3 - 106%),终末半衰期的调和均值为1098分钟,表明氟苯尼考在肌肉注射部位从制剂中缓慢释放。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验