食品科学

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超高效液相色谱-串联质谱法检测鱼中孔雀石绿、结晶紫及其代谢物

张艺蓓1,岳田利1,*,乔海鸥2,贾 如1,蒋旭鹏1,李 璐1   

  1. 1.西北农林科技大学食品科学与工程学院,陕西 杨凌 712100;
    2.陕西省疾病预防控制中心,陕西 西安 710054
  • 出版日期:2014-05-25 发布日期:2014-05-29
  • 通讯作者: 岳田利
  • 基金资助:

    2013年度西北农林科技大学“大学生创新创业训练计划”校级重点项目(1201310712174)

Determination of Malachite Green, Crystal Violet and Their Metabolites in Fishes by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry

ZHANG Yi-bei1, ,*, QIAO Hai-ou2, JIA Ru1, JIANG Xu-peng1, LI Lu1   

  1. 1. College of Food Science and Engineering, Northwest A & F University, Yangling 712100, China;
    2. Shaanxi Provincial Center for Disease Control and Prevention, Xi’an 710054, China
  • Online:2014-05-25 Published:2014-05-29
  • Contact: YUE Tian-li

摘要:

采用超高效液相色谱-串联质谱法同时测定鱼中孔雀石绿(malachite green,MG)、隐性孔雀石绿(leuco malachite green,LMG)、结晶紫(crystal violet,CV)、隐性结晶紫(leuco crystal violet,LCV)4 种物质残留。样品加入内标物D5-MG、D6-LMG、D5-CV、D6-LCV,经乙腈提取、离心、过中性氧化铝柱,氮气吹至近干,50%乙腈溶液定容,上机测定。MG和LMG线性范围为1~50 ng/mL,CV和LCV线性范围为1~100 ng/mL。4 种物质的检出限均为0.05 μg/kg,定量限均为0.15 μg/kg。在50、100、200 ng/mL 3 个添加水平下,回收率在87.80%~110.82%之间,相对标准偏差均小于等于4.32%(n=6)。该方法灵敏、准确、可靠,可以同时测定鱼中MG、LMG、CV、LCV残留。

关键词: 超高效液相色谱-串联质谱, 鱼, 孔雀石绿, 结晶紫, 残留

Abstract:

Purpose: Malachite green (MG), leuco malachite green (LMG), crystal violet (CV) and leuco crystal violet (LCV)
residues in fish were determined simultaneously using ultra performance liquid chromatography-tandem mass spectrometry
(UPLC-MS-MS). Methods: Fish samples after addition of internal standards D5-MG, D6-LMG, D5-CV, and D6-LCV were
extracted with acetonitrile and centrifuged, and then the supernatants were applied on a neutral alumina column, blown
almost dry under a stream of nitrogen and re-dissolved in 50% aqueous acetonitrile (by volume) before being subjected to
UPLC-MS-MS analysis. Results: A linear relationship was observed over a concentration range of 1–50 ng/mL for MG and
LMG, and over a concentration range of 1–100 ng/mL for CV and LCV. The limits of detection (LOD) for MG, LMG, CV
and LCV were 0.05 μg/kg and the limits of quantification (LOQ) for all of them were 0.15 μg/kg. Average recoveries from
blank samples spiked at levels of 50, 100 and 200 ng/mL ranged from 87.80% to 110.82%, with relative standard deviation
smaller than or equal to 4.32% (n = 6). Conclusions: This method proved sensitive, accurate and reliable.

Key words: ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS-MS), fish, malachite green(MG), crystal violet (CV), residues

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