畜牧兽医学报 ›› 2013, Vol. 44 ›› Issue (8): 1311-1316.doi: 10.11843/j.issn.0366-6964.2013.08.020

• 基础兽医 • 上一篇    下一篇

头孢噻呋在猪组织中残留消除规律

李帅鹏1,黄显会1,孔祥凯1,张晓会2,李向阳2   

  1. (1.华南农业大学国家兽药残留基准实验室,广州510642;2.洛阳惠中兽药有限公司,洛阳 471003)
  • 收稿日期:2013-03-18 出版日期:2013-08-23 发布日期:2013-08-23
  • 通讯作者: 黄显会, E-mail:xhhuang@scau.edu.cn
  • 作者简介:李帅鹏(1988-),男,河南省鲁山县人,硕士生,主要从事兽药残留检测和药物代谢动力学方面的研究,E-mail:1632762954@qq.com
  • 基金资助:

    公益性行业(农业) 科研专项(201303038-5)

Determination of Ceftiofur Residues in Swine Tissues

LI Shuai-peng1, HUANG Xian-hui1, KONG Xiang-kai1, ZHANG Xiao-hui2, LI Xiang-yang2   

  1. (1. National Reference Laboratory of Veterinary Drug Residues, South China Agricultural University, Guangzhou 510642, China; 2. Luoyang Huizhong Animal Medicine CO.LTD, Luoyang 471003, China)
  • Received:2013-03-18 Online:2013-08-23 Published:2013-08-23

摘要:

本研究旨在分析头孢噻呋在猪体内的残留消除规律,并为制定休药期提供依据。改进了猪可食性组织中头孢噻呋残留检测的高效液相色谱法(HPLC),试验猪按体重以5 mg·kg-1肌注给药,连续给药3 d,分别在最后一次给药后第12 小时及第3、5、7、9 天随机宰杀5头猪取样。样品先用二硫赤藓糖醇提取,再用碘乙酰胺衍生化后经MCX固相萃取小柱净化,经高效液相色谱C18柱分离后用紫外检测器检测。结果显示:给药后第12小时肾脏组织中的药物浓度最高,为2.589 μg·g-1,第3天所有组织的药物浓度均低于最高残留限量(MRL)。采用Winnonlin软件计算各组织的消除动力学参数,消除快慢依次为皮脂、肌肉、肝、肾和注射位点,其消除半衰期(t1/2β)分别为28.99、35.80、36.76、55.72和160.8 h。肾的药时曲线下面积(AUC)最高,为123.4 h·μg·g-1,说明肾脏是头孢噻呋作用的靶器官。参照EMEA对头孢噻呋制定的MRL,计算得注射位点的休药期最长,为98.64 h。结果提示水性头孢噻呋注射液吸收迅速,体内分布广,消除较快,建议休药期为5 d。

Abstract:

 This experiment was conducted to study tissue residues of ceftiofur in swine, preparing for determination of the withdrawal time. A confirmative method has been improved to determine ceftiofur residues in edible tissues of pigs by high-performance liquid chromatography (HPLC). Ceftiofur was administered to 30 healthy pigs intramuscularly at a dosage of 5 mg·kg1 for 3 consecutive days. Animals were sacrificed at 12 hours and the 3rd, 5th, 7th, 9th days after administration. The tissues were extracted with dithioerythritol, derivatized with iodoacetamide, and cleaned up on MCX solid-phase extraction cartridges. The analyte was detected by UV absorptive spectroscopy after separation by C18 column. The results showed that kidney had the highest drug concentration with 2.589 μg·g1 at 12 hours, while the concentration of ceftiofur in all of tissues at 3 days was lower than the Maximum Residue Limit (MRL). The pharmacokinetic parameters were estimated using Winnonlin software package. The results indicated that the elimination rate was skin/fatmuscleliverkidneyinjection site, with the elimination half-life of 28.99, 35.80, 36.76, 55.72, 160.8 h respectively. Compared with other tissues, the area under concentration-time curve (AUC) in kidney was highest with 123.4 h·μg·g1. Kidney was considered as the target organ. According to the MRL set by EU, the longest withdrawal time was suggested in injection site with 98.64 h. The results demonstrated that absorption and elimination was quickly and the distribution was wide. It is proposed that the withdrawal time was 5 days.

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