色谱 ›› 2014, Vol. 32 ›› Issue (6): 647-652.DOI: 10.3724/SP.J.1123.2014.01044

• 技术与应用 • 上一篇    下一篇

在线净化液相色谱-串联质谱法快速测定牛奶中的6种孕激素

段永生1, 王炳玲1, 艾连峰1, 郭春海1, 葛世辉1, 张婧雯1, 徐牛生2   

  1. 1. 河北出入境检验检疫局, 河北 石家庄 050051;
    2. 赛默飞世尔科技(中国)有限公司, 上海 201206
  • 收稿日期:2014-01-27 修回日期:2014-04-03 出版日期:2014-06-08 发布日期:2014-05-22
  • 通讯作者: 艾连峰
  • 基金资助:

    国家质检总局科技计划项目(2013IK154,2014IK092).

Determination of six progesterones in milk by on-line cleanup liquid chromatography-tandem mass spectrometry

DUAN Yongsheng1, WANG Bingling1, AI Lianfeng1, GUO Chunhai1, GE Shihui1, ZHANG Jingwen1, XU Niusheng2   

  1. 1. Hebei Entry-Exit Inspection and Quarantine Bureau, Shijiazhuang 050051, China;
    2. Thermo Fisher Scientific (China), Shanghai 201206, China
  • Received:2014-01-27 Revised:2014-04-03 Online:2014-06-08 Published:2014-05-22

摘要:

建立了在线净化液相色谱-串联质谱同时测定牛奶中炔诺酮、17α-羟基孕酮、甲羟孕酮、乙酸甲地孕酮、孕酮和醋酸美伦孕酮6种孕激素的方法。本方法采用乙腈为提取溶剂提取目标化合物。提取液经在线净化柱Cyclone-P净化,经Phenyl-Hexyl色谱柱分离,流动相采用0.5%(v/v)甲酸水溶液-乙腈,在电喷雾正离子模式下以多反应监测(MRM)方式测定,内标法定量。方法在0.1~50 μg/L范围内呈线性关系,线性相关系数均大于0.999。6种分析物的测定低限为0.5 μg/kg,在牛奶中3个水平的添加回收率在90.8%~107.5%之间,相对标准偏差在6.3%~11.8%之间。该方法快速简便,灵敏度高,选择性好,可用于牛奶样品中孕激素的快速定性定量分析。

关键词: 牛奶, 液相色谱-串联质谱, 孕激素, 在线净化

Abstract:

A new method using TurboFlow on-line cleanup liquid chromatography combined with tandem mass spectrometry (MS/MS) has been developed for simultaneous determination of six progesterones including 19-norethindrone, 17 α-hydroxyprogesterone, medroxyprogesterone, megestrol acetate, progesterone and melengestrol acetate in milk. Samples were extracted by acetonitrile. The analytes in extract were on-line purified directly on Cyclone-P purification column where the sample matrices were washed away. Subsequently, the analytes which were eluted from the extraction column onto Phenyl-Hexyl column were separated with a gradient elution, and detected with electrospray ionization mass spectrometry in the positive scan mode using multiple reaction monitoring (MRM). The isotope internal standards were employed for quantification. As a result, the linearities were satisfactory with the correlation coefficients of >0.999 at concentrations ranging from 0.1 μg/L to 50 μg/L. Based on the repeated analysis of a known blank sample, the limit of quantification (LOQ) is 0.5 μg/kg. Average recoveries of the analytes fortified at three levels (1, 5 and 25 μg/kg) ranged from 90.8% to 107.5%, and the relative standard deviations (RSDs) ranged from 6.3% to 11.8%. This proposed method is simple, rapid, sensitive and highly selective, and can be applied to simultaneous identification and quantification of the six progesterones in milk.

Key words: liquid chromatography-tandem mass spectrometry (LC-MS/MS), milk, on-line cleanup, progesterones

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