›› 2008, Vol. 10 ›› Issue (2): 88-93.

• 研究报告 • 上一篇    下一篇

麻保沙星在中国对虾体内药代动力学及残留研究

张海珍[1,2] 李健[2] 王群[2] 刘淇[2] 周一兵[1]   

  1. [1]大连水产学院生命科学与技术学院,辽宁大连116023 [2]中国水产科学研究院黄海水产研究所,农业部海洋渔业资源可持续利用重点开放实验室,山东青岛266071
  • 收稿日期:2008-02-28 修回日期:2008-03-05 出版日期:2008-04-15 发布日期:2009-07-29
  • 通讯作者: 李健,研究员,主要从事海水健康养殖和水产药理学研究。Tel:0532-85830183;E-mail:lijian@ysfri.ac.cn.
  • 作者简介:张海珍|硕士研究生|主要从事水产药理学研究。E-mail:oceanzhz@163.com。
  • 基金资助:

    国家科技支撑计划(2006BAD01A13),公益性农业行业科研专项(nyhyzx07-042)和科研院所社会公益研究专项(2004DIB4J165)资助.

Studies on Pharmacokinetics and Residues of |Marbofloxacin in Penaeus chinensis

ZHANG Hai-zhen, LI Jian| WANG Qun, LIU Qi, ZH0U, Yi-bing   

  1. 1. College of Life Sciences and Biotechnology, Dalian Fisheries University, Liaoning Dalian 116023 ; |2. Key 0pen Laboratory of Ministry of Agriculture for Sustainable Utilization of Marine FiShery Resources, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shandong Qingdao,266071, China
  • Received:2008-02-28 Revised:2008-03-05 Online:2008-04-15 Published:2009-07-29

摘要:

高效液相色谱法测定水温20±1℃条件下,2.5mg·kg^-1剂量肌注和口服麻保沙星在中国对虾体内的药代动力学及残留规律。采用3p97药动学软件处理数据,结果表明:肌注给药的药时数据符合一级吸收二室、开放模型,主要药动学参数如下:血淋巴、肌肉、肝胰腺内的Tmax和Cmax分别为0.147h.0.039h.0.103h和3.688μg·mL^-1、2.7331μg·mL^-1、4.524μg·mL^-1,AUC分别为8.474μg·mL^-1·h^-1、2.396μg·mL^-1·h^-1、18.310μg·mL^-1·h^-1(1/2)。为0.893h,0.103h、1.257h;t(1/2)B为9.866h、2.648h,4.947h,CL为0.118L·h^-1·kg^-1、1.043L·h^-1·kg^-1、0.137L·h^-1·k^-1。连续口服给药三种组织中消除半衰期分别为8.74h,55.14h.5.72h。根据本试验结果及多剂量给药原则,麻保沙星的合理给药方案为:口服2.5mg·kg^-1的剂量,每日1次给药。

关键词: 中国对虾 麻保沙星 药动学 残留

Abstract:

This paper reports pharmacokinetics and residues of marbofloxacin in Fenneropenaeus chinensis at 20 ± 1℃. Hemolymph、muscle and hepatopancreas were sampled after intrmuscular administration and repeat oral administration at a dose of 2.5mg·kg^- 1 body weight. The concentration of medicament in tisssues was determined by HPLC. The data were analyzed with the pharmacokinetics computer program 3p97. The concentration-time course of marbofloxacin in the tissues could be described by a two-compartment open model. The main pharmacokinetics parameters in hemo- lymph,muscle and hepatopancreas were as follows: Tmax 0. 147 h,0.039 h,0. 103 h; Cmax   3.688μg·mL^-1、2.731μg·mL^-1、4.524μg·mL^-1,AUC 8.474μg·mL^-1·h^-1、2.396μg·mL^-1·h^-1、18.3100μg·mL^-1·h^-1(1/2).0.893h,0.103h、1.257h;t(1/2)B 9.866h、2.648h,4.947h,CL 0.118L·h^-1·kg^-1、1.043L·h^-1·kg^-1、0.137L·h^-1·k^-1 After repeat oral administration, t(1/2)~were 8.74 h,5.14 h,5.72 h. Base on the data above, we suggested Fenneropenaeus chinensis could take marbofloxacin once per day by oral administration (2.5mg · kg^-1).

Key words: Fenneropenaeus chinensis , marbofloxaein , pharmaeokineties , residues

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