欢迎访问《中国临床药理学与治疗学》杂志官方网站,今天是 分享到:

中国临床药理学与治疗学 ›› 2006, Vol. 11 ›› Issue (5): 578-581.

• 研究原著 • 上一篇    下一篇

HPLC法测定头孢硫脒在家犬体内的浓度及其药代动力学

鲁澄宇, 许卫铭, 陈方1, 张小娜1, 吴铁   

  1. 广东医学院药理教研室, 湛江524023, 广东;
    1广州白云山制药股份有限公司, 广州510515, 广东
  • 收稿日期:2006-02-28 修回日期:2006-03-14 出版日期:2006-05-26 发布日期:2020-12-09
  • 通讯作者: 鲁澄宇, 男, 博士, 副教授, 研究方向:数学药理、中药现代化。 Tel:0759-2388588  E-mail:gdmclu @hotmail.com

Determination of cefathiamidine in dogs HPLC and its pharmacokinetics

LU Cheng-yu, XU Wei-ming, CHEN Fang1, ZHANG Xiao-na1, WU Tie   

  1. Department of Pharmacology , Guangdong Medical College, Zhanjiang 524023 , Guangdong, China;
    1Guangzhou Baiyunshan Pharmaceutical Co.Ltd , Guangzhou 510515 , Guangdong, China
  • Received:2006-02-28 Revised:2006-03-14 Online:2006-05-26 Published:2020-12-09

摘要: 目的: 建立犬体内头孢硫脒的血药浓度测定方法, 研究静脉注射头孢硫脒不同剂量(31.5 、63.0 、 126.0 mg·kg-1 ) 在犬体内的药代动力学。方法: 采用RT-HPLC 法测定犬静脉注射给药后不同时间血 浆中头孢硫脒的浓度。C18 反相色谱柱(Hypersil, 250 mm ×4.0 mm, 5 μm) , 流动相为乙睛∶磷酸盐缓 冲液(80∶20)。结果: 测定方法的最低检测浓度为 0.2 μg·ml-1 , 线性范围为0.2 ~ 50.0 μg·ml-1 , 回收 率在93.27 %~ 102.18 %。犬静注头孢硫脒后符合 开放二房室模型处置特征, 3 个剂量组主要药代动 力学参数如下:T1/2α为0.11 ±0.05, 0.13 ±0.03, 0.10 ±0.03 h;T1/2β为1.01 ±0.29, 0.84 ±0.17, 1.08 ±0.31 h;AUC 为14.3 ±1.2, 27.3 ±7.7, 74.4 ± 21.2 mg·L-1·h。结论: 本方法适合头孢硫脒的药动学研究, 测定结果为临床合理用药提供依据。

关键词: 头孢硫脒, 犬, HPLC, 药代动力学

Abstract: AIM: To develop a method for the determination of cefathiamidine in dog plasma and to study the pharmacokinetic characters following intravenous injection of cefathiamidine at varied doses (31.5, 63.0, 126. mg·kg-1 ) in dogs.METHODS: The concentrations of cefathiamidine in the plasma of dogs were determined by RT-HPLC.The determination has been performed on C18 column(Hypersil, 250 mm×4.0 mm, 5 μm ) with acetonitrile :phosphatic buffer (20 ∶80, v v ) as mobile phase.RESULTS: The method has good linearity between 0.2 -50.0 μg·ml-1 (r >0.999) with a limit of quantitation of 0.2 μg·ml-1.Recovery varied from 93.27 % -102.18 %.Pharmacokinetics of cefathiamidine could be described by the two compartment open models.The main pharmacokinetic parameters of cefathiamidine were as follows :T1/2αwere 0.11 ±0.05, 0.13 ± 0.03, 0.10 ±0.03 h;T1/2β were 1.01 ±0.29, 0.84 ± 0.17, 1.08 ±0.31 h;AUC were 14.3 ±1.2, 27.3 ± 7.7, 74.4 ±21.2 mg·L-1·h.CONCLUSION: The method can be used in pharmacokinetics of cefathiamidine and provided evidence for clinical application.

Key words: cefathiamidine, dog, HPLC, pharmacokinetics

中图分类号: