欢迎访问《渔业研究》官方网站,今天是 分享到:

›› 2018, Vol. 40 ›› Issue (4): 295-301.

• 论文与报告 • 上一篇    下一篇

超高效液相色谱-串联质谱法测定鱼肉中孔雀石绿及其代谢物的残留量

林功师   

  1. 厦门市海洋与渔业研究所
  • 收稿日期:2018-05-15 修回日期:2018-06-10 出版日期:2018-08-24 发布日期:2018-08-21
  • 通讯作者: 林功师

Determination of malachite green and metabolites residues in fish by ultra-high performance liquid chromatography-tandem mass spectrometry

Gong-Shi LIN   

  1. Xiamen Marine&Fisheries Research Institute
  • Received:2018-05-15 Revised:2018-06-10 Online:2018-08-24 Published:2018-08-21
  • Contact: Gong-Shi LIN

摘要: 对GB/T 19857—2005的方法进行优化,建立了鱼肉中孔雀石绿和隐色孔雀石绿残留量的超高效液相色谱-串联质谱分析方法。样品用乙腈提取,中性氧化铝小柱净化后,采用Zorbax Eclipse Plus-C18色谱柱进行分离,以乙腈-5 mmol/L乙酸铵缓冲溶液为流动相,以电喷雾正离子化模式(Electrospray ionization, ESI+)和多反应监测(Multiple reaction monitoring, MRM )扫描模式进行测定,同位素内标法定量。结果表明:孔雀石绿和隐色孔雀石绿含量在0.5~20.0 ng/mL的范围内线性关系良好(r>0.999),方法检出限均为0.05 μg/kg。在罗非鱼(Oreochromis mossambicus)、草鱼(Ctenopharyngodon idellus)、大菱鲆(Scophthalmus maximus)、鳜鱼(Siniperca chuatsi)、金鲳鱼(Trachinotus ovatus)、乌鳢(Ophiocephalus argus Cantor)6种鱼肉中添加水平为0.5、1.0、2.0 μg/kg时,目标物的平均回收率为 81.3%~103.3%,测定结果的相对标准偏差均小于 10%(n=6)。该方法定量准确、分析时间短、试剂用量少,适用于鱼肉中孔雀石绿及其代谢物残留量的定量检测。

关键词: 超高效液相色谱-串联质谱, 鱼肉, 孔雀石绿, 隐色孔雀石绿, 代谢物, ultra-high performance liquid chromatography-tandem mass spectrometry, fish, malachite green, leucomalachite green, metabolite

Abstract: This paper optimized the method of GB/T 19857—2005, and established a method for determination of malachite green (MG) and leucomalachite green (LMG) residues in fish through ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS).The samples were extracted with acetonitrile, cleaned up with neutral alumina column, and separated by Zorbax Eclipse Plus-C18 chromatographic column. The acetonitrile-5 mmol/L ammonium acetate buffer solution was used as mobile phase. Then aims compound were detected by UHPLC-MS/MS with ESI positive ion mode and multiple reactions monitoring (MRM) mode, and quantified by using isotope internal standards. The results showed that both MG, LMG contents had good linear relationship within the range of 0.5~20.0 ng/mL, and the correlation coefficient was 0.999. The detection limits was 0.05 μg/kg. The average recoveries ranged from 81.3% to 103.3% at the spiked levels of 0.5, 1.0, and 2.0 μg/kg in Oreochromis mossambicus, Ctenopharyngodon idellus, Scophthalmus maximus, Siniperca chuatsi, Trachinotus ovatus, and Ophiocephalus argus Cantor. The relative standard deviation of determination results was less than 10% (n=6). These results suggested that the method was accurate, rapid and saving reagents, which would be suitable for the detection of MG and LMG residues in fish.

中图分类号: