食品科学

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亲水液相色谱-串联质谱法测定羊肌肉组织中安乃近代谢物的残留量

张 崇1,2,薛飞群2,张丽芳2,张晓晓2,王霄旸2,江善祥1,*   

  1. 1.南京农业大学动物医学院,兽医药理与毒理实验室,江苏 南京 210095;
    2.中国农业科学院上海兽医研究所,兽药安全评价与兽药残留重点开放实验室,上海 200241
  • 出版日期:2014-05-25 发布日期:2014-05-29
  • 通讯作者: 江善祥
  • 基金资助:

    2013年农业部农业行业标准制修订项目(2013-550)

Simultaneous Determination of Residues of Four Dipyrone Metabolites in Goat Muscle by Hydrophilic Interaction Liquid Chromatography-Mass Spectrometry

ZHANG Chong1,2, XUE Fei-qun2, ZHANG Li-fang2, ZHANG Xiao-xiao2, WANG Xiao-yang2, JIANG Shan-xiang1,*   

  1. 1. Laboratory of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Nanjing Agricultural University,
    Nanjing 210095, China; 2. Key Laboratory of Veterinary Drug Safety Evaluation and Residue Research,
    Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China
  • Online:2014-05-25 Published:2014-05-29
  • Contact: JIANG Shan-xiang

摘要:

建立了羊肌肉组织中安乃近4 种主要代谢物——4-甲氨基安替比林、4-氨基安替比林、4-甲酰氨基安替比林和4-乙酰氨基安替比林的亲水液相色谱-串联质谱分析方法。肌肉样品均质后,用体积分数为5%的氨水乙腈提取,提取液用Cleanert PSA初步净化,60 ℃氮气吹干,乙腈复溶后过MAX(SPE)柱净化,采用亲水液相色谱-串联质谱测定,4 种物质均采用外标法定量。结果显示:4-甲氨基安替比林、4-甲酰氨基安替比林和4-乙酰氨基安替比林在添加量为4~200 μg/kg范围内线性良好;4-氨基安替比林在添加量为40~2 000 μg/kg范围内线性良好。在5、50、100、1 000 μg/kg 4 个添加量,回收率在75.02%~116.2%范围内。日内变异系数为1.63%~15.12%(n=5),日间变异系数均小于11%(n=15)。4-甲氨基安替比林、4-甲酰氨基安替比林和4-乙酰氨基安替比林的检测限均为0.5 μg/kg,4-氨基安替比林的检测限为5 μg/kg。该方法灵敏度高、重复性好,适用于羊肌肉组织中安乃近4 种主要代谢物的大批量样品检测。

关键词: 羊肌肉, 安乃近代谢物, 亲水液相色谱-串联质谱法

Abstract:

A hydrophilic interaction liquid chromatography-mass spectrometry (HILIC-MS) method was developed for
the determination of four dipyrone metabolites, namely 4-methylaminoantipyrine (MAA), 4-aminoantipyrine (AA),
4-formylaminoantipyrine (FAA), and 4-acetylaminoantipyrine (AAA) in goat muscle. These metabolites were extracted with
acetonitrile mixed with 5% ammonia. The extracts were cleaned up with Cleaner PSA, and then blow-dried by nitrogen gas,
re-dissolved in acetonitrile and re-cleaned up using MAX (SPE) cartridge. After chromatographic separation, the analytes were
quantified by the external standard method. The calibration curves were linear between 4 and 200 μg/kg matrix equivalent
concentrations for MAA, FAA, and AAA, and between 40 and 2 000 μg/kg for AA. The mean recoveries in blank samples
at four spike levels (5, 50, 100, and 1 000 μg/kg) ranged between 75.02% and 116.2%. The intra-day coefficient of variation
(CV) was 1.63% to 15.12% (n = 5), and the inter-day CV was less than 11% (n = 15). The detection limits were 0.5 μg/kg
for MAA, FAA and AAA and 5 μg/kg for AA. The proposed method is sensitive and repeatable, allowing analysis of a large
number of samples in a working day.

Key words: goat muscle, dipyrone metabolites, hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry

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