食品科学 ›› 2014, Vol. 35 ›› Issue (6): 142-145.doi: 10.7506/spkx1002-6630-201406030

• 分析检测 • 上一篇    下一篇

高效液相色谱-二极管阵列检测器-荧光检测器法测定植物油中的18 种多环芳烃

王 峰1,张志杰1,林 慧1,仓义鹏2,*   

  1. 1.江苏省产品质量监督检验研究院,江苏 南京 210007;2.宿迁市产品质量监督检验所,江苏 宿迁 223800
  • 收稿日期:2013-12-13 修回日期:2014-03-13 出版日期:2014-03-25 发布日期:2014-04-04
  • 通讯作者: 仓义鹏 E-mail:wdymch05@hotmail.com
  • 基金资助:

    江苏省质量技术监督局项目(KJ133810);苏州市常熟市科技局社会发展项目(CS201306)

Determination of 18 Polycyclic Aromatic Hydrocarbons in Vegetable Oil by High Performance Liquid Chromatography with Diodearry Detector and Fluorescence Detector

WANG Feng1, ZHANG Zhi-jie1, LIN Hui1, CANG Yi-peng2,*   

  1. 1. Jiangsu Provincial Supervising & Testing Research Institute for Product Quality, Nanjing 210007, China;
    2. Suqian Product Quality Supervision and Testing Institute, Suqian 223800, China
  • Received:2013-12-13 Revised:2014-03-13 Online:2014-03-25 Published:2014-04-04
  • Contact: CANG Yi-peng E-mail:wdymch05@hotmail.com

摘要:

建立凝胶渗透色谱法净化样品、高效液相色谱-二极管阵列串联荧光检测器法同时测定植物油中18 种多环芳烃的检测方法。样品经环己烷-乙酸乙酯(1∶1,v/v)溶解,利用凝胶渗透色谱法去除油脂大分子,PAH C18柱分离,乙腈和水作流动相进行梯度洗脱,设置荧光检测程序,以2 个发射波长通道同时采集数据,测定油样中的17 种多环芳烃,以二极管阵列检测器测定苊烯。结果表明:方法检出限为0.5~4 ng/mL,样品回收率在78.65%~103.4%之间,相对标准偏差小于5%。本方法满足德国标准对18 种多环芳烃的同步检测新要求。

关键词: 植物油, 多环芳烃, 高效液相色谱, 荧光检测器

Abstract:

A method has been developed for the simultaneous determination of 18 polycyclic aromatic hydrocarbons in
vegetable oil by gel permeation chromatography (GPC) and high performance liquid chromatography with diodearray
detector and fluorescence detector (HPLC-DAD-FLD). The samples were dissolved in cyclohexane-ethyl acetate (1:1, V/V),
then purified with GPC to remove grease molecules, and separated on a PAH C18 column using acetonitrile and water as the
mobile phase with gradient elution. Subjected to 2-wavelength channel data acquisition setting with fluorescence procedure,
17 kinds of polycyclic aromatic hydrocarbons in oil samples were determined. Data acquisition of acenaphthylene was
achieved by DAD detector. The detection limit of this method was 0.5–4 ng/mL. The average recovery rate in oil was in the
range of 78.65%–103.4% with relative standard deviation (RSD) of less than 5%. This method was satisfactorily used for
the simultaneous detection of 18 kinds of polycyclic aromatic hydrocarbons (PAHs) in edible oil, while meeting the new
detection requirements of Germany standards for these PAHs.

Key words: vegetable oil, polycyclic aromatic hydrocarbons (PAHs), high performance liquid chromatography (HPLC), fluorescence detector

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