张续, 王君, 朱英. 鱼肉中4种喹诺酮类药物的高效液相色谱串联质谱测定方法[J]. 环境卫生学杂志, 2018, 8(6): 507-512. DOI: 10.13421/j.cnki.hjwsxzz.2018.06.013
    引用本文: 张续, 王君, 朱英. 鱼肉中4种喹诺酮类药物的高效液相色谱串联质谱测定方法[J]. 环境卫生学杂志, 2018, 8(6): 507-512. DOI: 10.13421/j.cnki.hjwsxzz.2018.06.013
    ZHANG Xu, WANG Jun, ZHU Ying. Simultaneous Determination of 4 Quinolones Residues in Fish by High-performance Liquid Chromatography/Electrospray Tandem Mass Spectrometry[J]. Journal of Environmental Hygiene, 2018, 8(6): 507-512. DOI: 10.13421/j.cnki.hjwsxzz.2018.06.013
    Citation: ZHANG Xu, WANG Jun, ZHU Ying. Simultaneous Determination of 4 Quinolones Residues in Fish by High-performance Liquid Chromatography/Electrospray Tandem Mass Spectrometry[J]. Journal of Environmental Hygiene, 2018, 8(6): 507-512. DOI: 10.13421/j.cnki.hjwsxzz.2018.06.013

    鱼肉中4种喹诺酮类药物的高效液相色谱串联质谱测定方法

    Simultaneous Determination of 4 Quinolones Residues in Fish by High-performance Liquid Chromatography/Electrospray Tandem Mass Spectrometry

    • 摘要:
      目的 研制同时测定鱼肉中诺氟沙星、恩诺沙星、氧氟沙星和环丙沙星4种喹诺酮类药物残留的高效液相色谱-串联质谱方法(HPLC-MS/MS)。
      方法 鱼肉样品在McⅡvaine缓冲条件下采用乙腈超声提取,HLB固相萃取柱净化;选用Shim-pack XR-ODS Ⅲ C18色谱柱,以0.1%甲酸水溶液和甲醇为流动相进行梯度洗脱;正离子电喷雾多反应监测模式(MRM)测定4种喹诺酮类药物残留。
      结果 4种喹诺酮类药物在(0.5~100)ng/g线性范围内线性关系良好,相关系数均>0.995。诺氟沙星、恩诺沙星、氧氟沙星和环丙沙星的检出限(3S/N)分别为0.7、0.15、0.15和0.7 ng/g,定量限(10S/N)分别为2.5、0.5、0.5和2.5 ng/g。实际样品在5、10、50 ng/g 3个含量水平的加标回收率80.4%~104%,相对标准偏差为3.2%~9.5%。
      结论 本方法操作简便,灵敏度高,检出限低,可用于鱼肉中4种喹诺酮类药物残留的测定。

       

      Abstract:
      Objectives To develop an analytical method for simultaneous determination of the residues of 4 quinolones (norfloxacin, enrofloxacin, ofloxaxin and ciprofloxacin) in fish by high performance liquid chromatography/electrospray tandem mass spectrometry (HPLC-MS/MS).
      Methods Samples were extracted with acetonitrile in McⅡvaine buffer, and then purified by solid phase extraction cartridge (HLB), separated on a ShimpackXR-ODSⅢ C18 column, and gradient eluted with 0.1% formic acid aqueous solution and methanol. The quantification of four quinolones was achieved under a multiple reaction monitoring (MRM) mode by positive electro spray (ESI+).
      Results There was a good linearity in the range of (0.5~100) ng/g for four quinolones, with a linear correlation coefficient of >0.995. The limit of detection for norfloxacin, enrofloxacin, ofloxaxin and ciprofloxacin were 0.7, 0.15, 0.15 and 0.7 ng/g, respectively. The limit of quantification for norfloxacin, enrofloxacin, ofloxaxin and ciprofloxacin were 2.5, 0.5, 0.5 and 2.5 ng/g, respectively. The recovery rates spiked at 5, 10 and 50 ng/g were in the range of 80.4%~104% with a relative standard deviation (RSD) of 3.2%~9.5%.
      Conclusions This method was reliable with high sensitivity, good recovery and repeatability. It was suitable for the determination of quinolones residues in fish.

       

    /

    返回文章
    返回