食品科学 ›› 2017, Vol. 38 ›› Issue (22): 291-297.doi: 10.7506/spkx1002-6630-201722043

• 安全检测 • 上一篇    下一篇

高效液相色谱-串联质谱法测定牛奶和鸡肉中4 种激素本底值

孙利东,许秀丽,袁飞,聂雪梅,许博舟,洪云鹤,张峰   

  1. (1.中国检验检疫科学研究院食品安全研究所,北京 100176;2.内蒙古满洲里出入境检验检疫局技术中心,内蒙古?满洲里 021400)
  • 出版日期:2017-11-25 发布日期:2017-11-03
  • 基金资助:
    “十三五”国家重点研发计划重点专项(2016YFD0401103;2016YFF0203903)

High Performance Liquid Chromatography-Tandem Mass Spectrometry Method for Simultaneous Determination of Background Values of 4 Hormones in Milk and Chicken

SUN Lidong, XU Xiuli, YUAN Fei, NIE Xuemei, XU Bozhou, HONG Yunhe, ZHANG Feng   

  1. (1. Institute of Food Safety, Chinese Academy of Inspection and Quarantine, Beijing 100176, China;2. Technology Center of the Manzhouli Entry-Exit Inspection and Quarantine Bureau, Manzhouli 021400, China)
  • Online:2017-11-25 Published:2017-11-03

摘要: 建立牛奶和鸡肉中4 种激素(睾酮、甲基睾酮、孕酮、氢化可的松)本底值同时测定的高效液相色谱-串联质谱方法。样品经β-葡萄糖醛酸酶/芳香基硫酸酯酶水解,加入乙腈超声提取,正己烷除脂肪。采用ZORBAX SB-C18色谱柱分离,以0.1%甲酸溶液和甲醇为流动相梯度洗脱,分别在电喷雾离子源正、负离子模式下以多反应监测模式分段扫描同时检测,基质匹配外标法定量。结果表明,4?种激素在相应的质量浓度范围内线性良好,相关系数均大于0.991;在牛奶中的检出限(RSN=3)和定量限(RSN=10)分别为0.02~0.10?μg/kg和0.06~0.33?μg/kg,在鸡肉中的检出限和定量限分别为0.03~0.12?μg/kg和0.10~0.40?μg/kg;在3?个水平下的平均回收率为牛奶56.0%~132.8%,鸡肉79.6%~122.0%;相对标准偏差为牛奶1.8%~17.3%,鸡肉2.0%~18.1%。该方法简单、快速、准确,适用于对牛奶和鸡肉中4?种激素进行快速筛查和本底值测定。

关键词: 激素, 鸡肉, 牛奶, 本底值, 高效液相色谱-串联质谱法

Abstract: A high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the simultaneous determination of background values of 4 hormones (testosterone, methyltestosterone, progesterone and hydrocortisone) in milk and chicken. The samples were hydrolyzed by β-glucuronidase and ultrasonically extracted with acetonitrile, and then the extract was defatted with hexane. The analytes were seperated on a ZORBAX SB-C18 column with methanol-0.1% formic acid as mobile phase by gradient elution. The mass spectrometer was run in multiple reaction monitoring mode (MRM) using positive- and negative-ion electrospray ionization (ESI), respectively. The quantitative analysis was carried out by matrix-matched external standard method. The results showed that the calibration curves had good linearity for 4 hormones in the tested concentration ranges, with correlation coefficients of more than 0.991. The limits of detection (LOD, RSN = 3) and limits of quantitation (LOQ, RSN = 10) were 0.02–0.10 and 0.06–0.33 μg/kg in milk, and 0.03–0.12 μg/kg and 0.10–0.40 μg/kg in chicken, respectively. The average recoveries at three spiked levels 56.0%–132.8% for milk and 79.6%–122.0% for chicken, and the precisions expressed as relative standard deviations (RSDs) were 1.8%–17.3% for milk and 2.0%–18.1% for chicken. The method proved to be simple, rapid, accurate, and suitable for rapid screening and detection of background values for 4 hormones in milk and chicken.

Key words: hormones, chicken, milk, background values, high performance liquid chromatography-tandem mass spectrometry

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