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›› 2013, Vol. 35 ›› Issue (6): 441-447.

• 论文与报告 • 上一篇    下一篇

气相色谱-质谱法检测鱼肉中MS-222残留

刘海新1,张农2,余颖1,姜琳琳1,李庐峰1,王艳君1   

  1. 1. 福建省水产研究所
    2.
  • 收稿日期:2013-09-22 修回日期:2013-10-14 出版日期:2013-12-25 发布日期:2013-12-23
  • 通讯作者: 刘海新
  • 基金资助:
    福建省科技厅资助项目 公益类科研院所专项(2011R1003-4)

Studies on detecting MS-222 residues in fish meat by GC-MS

  • Received:2013-09-22 Revised:2013-10-14 Online:2013-12-25 Published:2013-12-23
  • Contact: Hai-Xin LIU

摘要: 本文建立了鱼肉中MS-222残留GC-MS检测方法。鱼肉样品经乙腈提取,氮吹浓缩,盐酸溶液引导MS222电离,Waters Oasis MCX固相萃取柱净化后,气相色谱-四极杆质谱检测。方法检出限为2.5 μg.kg-1,定量限为5.0 μg.kg-1;0.0025~1.0μg.mL-1范围内线性关系良好(r≥0.9996);MS-222浓度范围在5.0~100.0μg.kg-1的鱼肉加标样,日内和日间平均回收率为78.4%~91.2%,相对标准偏差为3.62%~9.49%。实验结果表明,该检测方法适用于低浓度水平鱼肉中MS-222残留检测。

关键词: MS222, 气相色谱-质谱, 鱼肉, MS-222, gas chromatohraph-mass spectrum, fish meat

Abstract: A method is established for detecting MS-222 in fish meat by GC-MS. The MS-222 residues is extracted with acetonitrile, ionized in HCL solution, isolated by Waters Oasis MCX SPE column, then detected by GC-Quadrupole Mass Spectrometer. The limits of quantification is 5.0μg?kg-1, linear correlation coefficients of calibration curve is over 0.9996 within the concentration range of 0.0025~1.0μg?mL-1, For the 5.0~100.0μg?kg-1 spiked sample, within-day and day-to-day average recoveries are 78.4~91.2%, RSDs are 3.62~9.49%. From the results of above, this method can be used to detect the low concentration MS222 in fish meat.

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