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超高效液相色谱-串联质谱法同时测定饲料中的7种β2-兴奋剂

Simultaneous Determination of 7 Kinds of β2-agonist in Feed by UPLC-MS/MS

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【作者】 卢艳芬徐丽君王辉王志明颜克旭

【Author】 LU Yan-fen,XU Li-jun,WANG Hui,WANG Zhi-ming,YAN Ke-xu (Changsha Quality Testing Center of Livestock Poultry and Aquatic Products,Changsha 410013,China)

【机构】 长沙市畜禽水产品质量检测中心

【摘要】 为了准确测定饲料中7种β2-兴奋剂,建立了超高效液相色谱-串联质谱检测方法。样品经酸性有机混合溶剂提取、固相萃取净化浓缩后,在多反应监测模式下,用带电喷雾离子源(ESI)的串联质谱仪对样品进行定性和定量分析。该方法下各化合物定量检出限为50μg/kg。在50、100、200μg/kg的添加浓度下,回收率在71%~103%之间,相对标准偏差在5.7%~9.8%之间。本方法快速、准确、灵敏度高,适合饲料中福莫特罗、苯乙醇胺A、克仑特罗、莱克多巴胺、沙丁胺醇、特布它林、西马特罗的同时快速检测。

【Abstract】 A method of ultra performance liquid chromatograghy-electrospray tandem mass spectrometry(UPLC-MS/MS) was studied for determination of β2-agonist in feed.The sample was extracted by 0.1 mol/L hydrochloric acid-methanol mixed solvent,purified and enriched with cationic solid phase extraction column,and which was separated by liquid chromatography on C18 column with mobile phase of 0.1% formic acid in methanol(gradient elution),then analyzed in UPLC-MS/MS with electrospray ion source(ESI) under multi-reaction monitor mode(MRM).The quantification was performed with external standard method.The method has a lower limit of quantitation 50 μg/kg.Spike recoveries of three concentration addition levels(50,100,200 μg/kg) ranged in 71%—103% with relative standard deviations in 5.7%—9.8%.The method is fast,accurate and sensitive.It is suitable for rapid qualitative and quantitative detection of β2-agonist in animal feed.

【基金】 长沙市科技局现代农业与健康科技重大专项(K1003024-21)资助
  • 【文献出处】 质谱学报 ,Journal of Chinese Mass Spectrometry Society , 编辑部邮箱 ,2012年05期
  • 【分类号】S816;O657.63
  • 【被引频次】18
  • 【下载频次】159
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