色谱 ›› 2020, Vol. 38 ›› Issue (2): 224-231.DOI: 10.3724/SP.J.1123.2019.04046

• 研究论文 • 上一篇    下一篇

超高效液相色谱-三重四极杆质谱法检测油脂和油炸食品中7种杂环胺类物质

张晨霞, 马宇翔, 赵天培, 席俊, 李潘, 郭庆, 史莉莉, 汪学德()   

  1. 河南工业大学粮油食品学院, 河南 郑州 450001
  • 收稿日期:2019-04-29 出版日期:2020-02-08 发布日期:2020-12-10
  • 通讯作者: 汪学德
  • 作者简介:汪学德.Tel:(0371)67758025, E-mail:wangxuede1962@126.com
  • 基金资助:
    国家重点研发计划(2017YFC1600402-3);现代农业产业技术体系建设项目(CARS14-1-29);河南工业大学"科教融合"项目(26400109)

Determination of seven heterocyclic aromatic amines in oils and fried foods by ultra performance liquid chromatography-triple quadrupole mass spectrometry

ZHANG Chenxia, MA Yuxiang, ZHAO Tianpei, XI Jun, LI Pan, GUO Qing, SHI Lili, WANG Xuede()   

  1. College of Food Science and Technology, Henan University of Technology, Zhengzhou 450001, China
  • Received:2019-04-29 Online:2020-02-08 Published:2020-12-10
  • Contact: WANG Xuede
  • Supported by:
    National Key Research and Development Program of China(2017YFC1600402-3);Modern Agro-Industry Technology Research System(CARS14-1-29);Science and Education Integration Project of Henan University of Technology(26400109)

摘要:

建立了检测油脂及油炸食品中7种杂环胺类物质的超高效液相色谱-三重四极杆质谱(UPLC-MS/MS)的检测方法。以含1%(体积分数)氨水的乙腈溶液为提取液,采用乙腈饱和的正己烷脱脂,以PCX固相萃取柱为净化柱,10 mmol/L甲酸铵溶液(pH 6.8)和乙腈为流动相,采用Waters ACQUITY UPLC BEH C18反相色谱柱(50 mm×2.1 mm,1.7 μm)梯度洗脱,流速为0.3 mL/min,在正离子扫描、多反应监测模式下测定,内标法定量。结果表明,杂环胺类物质在各自范围内,线性关系良好,相关系数大于0.999;在3个加标水平下,杂环胺类物质在油脂和油炸食品中的平均回收率为64.31%~113.8%,相对标准偏差为0.18%~9.26%,检出限(S/N=3)和定量限(S/N=10)分别为0.01~0.14 ng/g和0.09~0.38 ng/g。该方法具有灵敏、准确等优点,适用于油脂和油炸食品中杂环胺的确证检测。

关键词: 超高效液相色谱, 三重四极杆质谱, 固相萃取, 杂环胺, 油脂, 油炸食品

Abstract:

An ultra performance liquid chromatography-triple quadrupole mass spectrometry (UPLC-MS/MS) method was developed for the determination of seven heterocyclic aromatic amines (HCAs) in oil and fried food samples. The samples were extracted with acetonitrile containing 1% (v/v) ammonia water, defatted by n-hexane saturated with acetonitrile, and cleaned up with PCX solid phase extraction column. The extracts were separated on a Waters ACQUITY UPLC BEH C18 reversed-phase column (50 mm×2.1 mm, 1.7 μm) with gradient elution by using acetonitrile-10 mmol/L ammonium formate aqueous solution as the mobile phase. Quantitative detection was performed by using a positive-ion electrospray ionization source in the multiple reaction monitoring (MRM) mode, employing an internal isotope standard. The method showed good linear relationships in the range of 0.5-100 μg/L for the seven HCAs with correlation coefficients (R2)>0.999. The average recoveries ranged from 64.31% to 113.8% with the relative standard deviations of 0.18%-9.26% at the three spiked levels in oil and fried food samples. The limits of detection (LODs) and limits of quantification (LOQs) were 0.01-0.14 ng/g and 0.09-0.38 ng/g, respectively. The method is sensitive, accurate, and suitable for the determination and confirmation of the seven HCAs in oil and fried food samples.

Key words: ultra performance liquid chromatography (UPLC), triple quadrupole mass spectrometry (MS/MS), solid phase extraction (SPE), heterocyclic aromatic amines (HCAs), oils, fried foods