食品科学

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高效液相色谱-串联质谱测定以蜂胶为主要原料的保健食品中氯霉素

杨 黎,廖夏云,杨玮婷,许杨彪,刘向红,刘珈伶,鲁毅翔,郭雯雯,林小娟   

  1. 1.广西食品药品检验所,广西 南宁 530021;2.广西-东盟食品药品安全检验检测中心,广西 南宁 530021;
    3.广西中医药大学药学院,广西 南宁 530021;4.四川省成都市锦江区人民检察院,四川 成都 610021
  • 出版日期:2016-08-25 发布日期:2016-08-30
  • 通讯作者: 刘向红
  • 基金资助:

    2014年广西食品药品检验所科技项目(KY201410);广西高校科技创新能力提升工程专项(ZJGX201403002)

Determination of Chloramphenicol in Propolis-Derived Health Foods by HPLC-MS/MS

YANG Li, LIAO Xiayun, YANG Weiting, XU Yangbiao, LIU Xianghong, LIU Jialing, LU Yixiang, GUO Wenwen, LIN Xiaojuan   

  1. 1. Guangxi Institute for Food and Drug Control, Nanning 530021, China; 2. Guangxi-ASEAN Food and Drug Safety Inspection and
    Testing Center, Nanning 530021, China; 3. College of Pharmacy, Guangxi University of Chinese Medicine, Nanning 530021, China;
    4. The People’s Procuratorate of Jinjiang Chengdu, Chengdu 610021, China
  • Online:2016-08-25 Published:2016-08-30
  • Contact: LIU Xianghong

摘要:

建立高效液相色谱-串联质谱测定以蜂胶为主要原料的保健食品中氯霉素残留方法。样品经质量分数0.5%Ca(OH)2混悬液溶解,以盐酸酸化除杂,再用乙酸乙酯进行反萃取,采用Inertsil C8-3(2.1 mm×100 mm,2 μm)色谱柱进行分离,流动相为甲醇-水,梯度洗脱,电喷雾负离子多反应监测模式检测氯霉素。结果显示,氯霉素在0.1~2.0 ng/mL范围线性关系良好,在0.1、0.2、1.0 μg/kg三个水平条件下,绝对回收率为58.3%~74.5%,相对标准偏差为1.34%~5.11%;相对回收率为96.8%~114.0%,相对标准偏差为1.33%~5.36%,检出限为0.04 μg/kg。该方法灵敏度高、重复性好,可满足以蜂胶为主要原料的保健食品中痕量氯霉素残留的测定。

关键词: 高效液相色谱-串联质谱, 蜂胶, 保健食品, 氯霉素

Abstract:

A high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was established
to detect chloramphenicol residue in propolis-derived health foods. Samples were dissolved in 0.5% Ca(OH)2 solution,
followed by the removal of mucinous impurities after treatment with hydrochloric acid. Then chloramphenicol was back
extracted with ethyl acetate. The extract was separated on an Inertsil C8-3 column (2.1 mm × 100 mm, 2 μm) with gradient
elution using a mobile phase consisting of methanol and water. A tandem quadrupole mass spectrometer equipped with
electrospray ionization (ESI) source in positive ion mode was employed for the quantitative analysis of the analyte using
multiple reaction monitoring (MRM). The calibration curve for chloramphenicol displayed good linearity in the range of
0.1–2.0 ng/mL. The limit of detection (LOD) of the proposed method was 0.4 ng/mL. The absolute recoveries were 58.3%–
74.5% at spiked concentration levels of 0.1, 0.2, and 1.0 μg/kg with relative standard deviations (RSDs) of 1.34%–5.11%,
and the relative recoveries were 96.8%–114.0% with RSDs of 1.33%–5.36%. The method exhibited high sensitivity and
good reproducibility, and could be suitable for the determination of trace amounts of chloramphenicol in propolis-derived
health foods.

Key words: HPLC-MS/MS, propolis, health foods, chloramphenicol

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