食品科学 ›› 2022, Vol. 43 ›› Issue (4): 299-304.doi: 10.7506/spkx1002-6630-20210223-242

• 安全检测 • 上一篇    下一篇

固相萃取结合高效液相色谱-串联质谱法测定鸡蛋中那西肽残留

肖陈贵,沈金灿,朱萍萍,赵凤娟,郭伟杰,康海宁,岳振峰   

  1. (深圳海关食品检验检疫技术中心,深圳市食品安全检测技术研发重点实验室,广东 深圳 518045)
  • 出版日期:2022-02-25 发布日期:2022-03-08
  • 基金资助:
    “十三五”国家重点研发计划重点专项(2017YFC1601603)

Determination of Nosiheptide Residues in Eggs by Dispersive Solid Phase Extraction Combined with High Performance Liquid Chromatography-Tandem Mass Spectrometry

XIAO Chengui, SHEN Jincan, ZHU Pingping, ZHAO Fengjuan, GUO Weijie, KANG Haining, YUE Zhenfeng   

  1. (Shenzhen Key Laboratory of Edtection Technology R&D on Food Safety, Food Inspection & Quarantine Center, Shenzhen Customs District, Shenzhen 518045, China)
  • Online:2022-02-25 Published:2022-03-08

摘要: 建立鸡蛋样品中那西肽的高效液相色谱-串联质谱检测方法。样品经甲酸-乙腈溶液提取后,正己烷除脂,再经HLB固相萃取柱净化;样品溶液通过高效液相色谱-串联质谱进行检测,采用负离子模式电喷雾电离,配合多反应离子扫描分析目标化合物。分别对样品前处理条件及色谱质谱参数进行优化。结果表明,采用1%甲酸-乙腈溶液萃取,经HLB固相萃取净化,定容液用聚四氟乙烯滤膜过滤,以醋酸铵-乙腈作为流动相,能够实现那西肽的快速测定。在优化条件下采用基质标准曲线外标法定量分析,那西肽在1.0~20.0 μg/L质量浓度范围内线性关系良好,相关系数R2大于0.998,方法的检出限为0.3 μg/kg,定量限为1.0 μg/kg。在1.0、2.0 μg/kg和10 μg/kg添加量下,那西肽的平均回收率为83.8%~96.2%,相对标准偏差为6.0%~8.8%。该方法简便快速、灵敏度高、准确性好,适用于鸡蛋中那西肽残留的监测。

关键词: 那西肽;固相萃取;高效液相色谱-串联质谱法;鸡蛋

Abstract: A method was established for the determination of nosiheptide in egg samples using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Egg samples were extracted with acidic acetonitrile, defatted with n-hexane and then purified by solid phase extraction (SPE) on an HLB cartridge. The extract was analyzed by HPLC-MS/MS in the negative electrospray ionization mode using multiple reaction monitoring (MRM). The sample pretreatment?and the experimental conditions were optimized. Fast analysis was achieved when the sample was extracted with 1% formic acid-acetonitrile, cleaned up on an Oasis HLB cartridge, and filtered with a porous polytetrafluoroethylene (PTFE) membrane and ammonium acetate-acetonitrile was used as the mobile phase. A matrix-matched standard calibration curve was prepared and external standard method was used for quantification under the optimal conditions. Good linearity was observed in the concentration range from 1.0 to 20.0 μg/L with a correlation coefficient over 0.998. The limit of detection was 0.3 μg/kg, and the limit of quantification was 1.0 μg/kg. The average recoveries at spiked levels of 1.0, 2.0 and 10 μg/kg were in the range from 83.8% to 96.2%, with relative standard deviations (RSDs) between 6.0% and 8.8%. In conclusion, the developed method is simple, fast, sensitive, accurate, and can be applicable for the detection of nosiheptide in egg samples.

Key words: nosiheptide; solid phase extraction; high performance liquid chromatography-tandem mass spectrometry; egg

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