食品科学 ›› 2018, Vol. 39 ›› Issue (16): 295-300.doi: 10.7506/spkx1002-6630-201816042

• 安全检测 • 上一篇    下一篇

分散固相萃取-超高效液相色谱-串联质谱法测定禽蛋中4 种内外源性孕激素

黄丽英1,邹?圆2,陆?强2,范栋杰1,顾?捷1,龙?举1,张月星2,*   

  1. (1.浙江省海洋水产研究所,浙江海洋大学海洋与渔业研究所,浙江?舟山 316021;2.浙江海洋大学海洋科学与技术学院,国家海洋设施养殖工程技术研究中心,浙江?舟山 316022)
  • 出版日期:2018-08-25 发布日期:2018-08-17
  • 基金资助:
    国家自然科学基金青年科学基金项目(31502182);浙江省科技计划项目(2017F50018;2017F50020); 浙江海洋大学“海洋科学”省重中之重学科开放课题(20160107)

Determination of 4 Endogenous and Exogenous Progesterone Hormones in Egg by Dispersive Solid-phase Extraction and Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry

HUANG Liying1, ZOU Yuan2, LU Qiang2, FAN Dongjie1, GU Jie1, LONG Ju1, ZHANG Yuexing2,*   

  1. (1. Marine Fisheries Research Institute of Zhejiang, Marine and Fishery Institute, Zhejiang Ocean University, Zhoushan 316021, China; 2. National Engineering Research Center of Marine Aquaculture, College of Marine Science and Technology, Zhejiang Ocean University, Zhoushan 316022, China)
  • Online:2018-08-25 Published:2018-08-17

摘要: 采用基质固相分散的前处理技术,建立禽蛋中4 种孕激素(孕酮、醋酸美伦孕酮、醋酸甲地孕酮、醋酸氯地孕酮)的超高效液相色谱-串联质谱检测技术。样品经正己烷提取氮吹浓缩后用甲醇溶液复溶,复溶液加入N-丙基乙二胺固相吸附剂净化,离心上清液经ACQUITY UPLC BEH C18柱(2.1?mm×100?mm,1.7?μm)分离,以0.1%甲酸溶液和甲醇为流动相梯度洗脱,在电喷雾正离子模式下以多反应监测方式测定。4?种孕激素在0.4~100?μg/L范围内线性关系良好,相关系数r2大于0.996,方法检出限为0.2?μg/kg,定量限为0.6?μg/kg。在3?个加标水平下禽蛋中4?种孕激素的平均回收率在79.5%~99.7%之间,相对标准偏差(n=6)均小于10.0%。该方法简便快捷、灵敏度高、实用性强,适用于禽蛋中4?种孕激素的日常检测。

关键词: 分散固相萃取, 禽蛋, 超高效液相色谱-串联质谱, 孕激素

Abstract: A method was established for the determination of four progesterones (progesterone, melengestrol acetate, megestrol acetate and chlormadinone acetate) by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) with dispersive solid-phase extraction. The samples were extracted with n-hexane and then the extract was redissolved with methanol solution after being evaporated to dryness by nitrogen blowing. The solution was then purified with primary secondary amine (PSA) solid phase adsorbent. Using binary mobile phase gradient with water containing 0.1% formic acid and methanol, the centrifugal supernatant was separated on an ACQUITY UPLC BEH C18 column (2.1 mm × 100 mm, 1.7 μm) and the target compounds were detected under a multiple reaction monitoring (MRM) mode with a positive electrospray ionization source. The results showed that the calibration curves for the four progesterone hormones exhibited good linear relationships in the range of 0.4–100 μg/L with correlation coefficients (r2) of more than 0.996. The limit of detection was 0.2 μg/kg and the limit of quantification was 0.6 μg/kg. The average recoveries at three spiked levels were 79.5%–99.7% with relative standard deviations (RSD, n = 6) of less than 10.0%. This method proved to be simple, rapid, highly sensitive and practical, and thus it could be applicable for routine determination of the 4 progesterone hormones in eggs.

Key words: dispersive solid-phase extraction, egg, ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), progesterone hormones

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