›› 2008, Vol. 1 ›› Issue (5): 68-71.

• 奶业专栏 • 上一篇    下一篇

盐酸环丙沙星在患子宫内膜炎奶牛子宫内给药的药物浓度

陶金忠1,2,3,杨国林3,李剑勇3,李世宏3,赵兴绪2,严作庭3,谢家声3,巩忠福3   

  1. 1.宁夏大学农学院,银川 750021;2.甘肃农业大学,兰州 730070;3.中国农业科学院兰州畜牧与兽药研究所,兰州 730050
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2008-05-20 发布日期:2008-05-20

Study of Pharmacokinetics of Ciprofloxacin Hydrochloride in the Blood of Endometritis Dairy Cow

TAO Jinzhong1,2,3, YANG Guolin3, LI Jianyong3, LI Shihong3, ZHAO Xingxu2,YAN Zuoting3, XIE Jiasheng3, GONG Zhongfu3
  

  1. 1.School of Agriculture of Ningxia University, Yinchuan 750021, China;2.Faculty of Veterinary Medicine of Gansu Agricultural University, Lanzhou 730070, China;3.Lanzhou Institute of Pasturage and Veterinary Medicine of Chinese Academy of Agricultural Sciences, Lanzhou 730050, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2008-05-20 Published:2008-05-20

摘要: 本研究以反相高效液相色谱为定量分析手段,选用5头患子宫内膜炎的奶牛,通过子宫内灌注盐酸环丙沙星(2.5 g/头),研究了盐酸环丙沙星在患子宫内膜炎奶牛体内的药物动力学规律。以二氟沙星为内标,血浆样品经甲醇沉淀蛋白,离心,经针头式过滤器处理,用反相高效液相法测定其中盐酸环丙沙星的浓度。 色谱条件为:ODS-1C18柱;测定流动相为0.015 mol/L四丁基溴化铵溶液-乙腈(92∶8,V/V),pH为3.0;流速为1.0 ml/min;荧光检测器,激发波长(λex)278 nm,发射波长(λem)465 nm。通过采用MCPKP房室分析程序,分析血中浓度时间数据,发现有3头奶牛血样药时数据符合无吸收三室开放模型。其血样中主要药动学参数为:T1/2α为0.916 h、T1/2β为49.20 h、AUC高达7.6296 mg/L·h、Clβ为1.582 L/kg·h,β为0.642 h-1。有2头奶牛血样药时数据符合一级吸收二室开放模型。其主要药动学参数为:T1/2α为1.26 h、T1/2β为9.2 h、AUC高达28.336 mg/L·h,β为0.3571 h-1。试验结果表明,盐酸环丙沙星子宫给药吸收快,分布广,消除慢。

关键词: 盐酸环丙沙星; 药动学; 反相高效液相色谱法; 子宫内膜炎; 奶牛

Abstract: The pharmacokinetics and residues of ciprofloxacin hydrochloride in the milk were investigated in 5 cows suffered from endometritis following singleintrauterine administration at the dosage of 2.5 per cow. Blood and milk were sampled at different intervals after administration and ciprofloxacin hydrochloride concentrations were determined by RP-HPLC method with a fluorescent detector. Difloxacin was used as intra-standard. The concentrationtime data were analyzed with MCPKP program. The ciprofloxacin hydrochloride concentrationtime data were fitted to a twocompartment open model with first order absorption in two cows suffered from endometritis after singleintrauterus. The main pharmacokinetics parameters were as follow: T 1/2α 1.26 h, T1/2β9.2 h, AUC 28.336 mg/L·h, β 0.3571 h-1. The ciprofloxacin hydrochloride concentration-time data were fitted to a three-compartment open model with nonabsorption in other three cows. The main pharmacokinetics parameters were as follow: T 1/2α0.916 h, T1/2β49.20 h, AUC 7.6296 mg/L·h,Clβ 1.582 L/kg·h, β 0.642 h-1. The results showed that ciprofloxaxin hydrochloride was absorbed fast and distributed extensively, but it was eliminated slowly in the blood after singleintrauterine administration.

中图分类号: