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液相色谱串联质谱法测定饲料中盐酸克伦特罗、莱克多巴胺、沙丁胺醇、苯乙醇胺A 被引量:18

Determination of Clenbuterol Ractopamine Salbuterol and Nylethanolamine in Feeds by Liquid Chromatography-Electrospray Tandem Mass Spectrometry
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摘要 利用液相色谱串联质谱(LC-ESI-MS/MS)测定饲料中盐酸克伦特罗、莱克多巴胺、沙丁胺醇、苯乙醇胺A。通过一系列实验对样品前处理条件进行了优化,样品经乙腈提取、乙酸酸化、净化后,采用HPLC-ESI-MS/MS检测分析,在多反应监测模式(MRM)下,外标法定量。方法的检出限为0.05 mg/kg,各组分浓度在0.001~0.2 mg/kg范围内与定量离子峰面积呈良好的线性关系(r>0.99)。平均加标回收率为61%~75%,测定结果的相对标准偏差为2.78%~4.37%(n=6)。该方法简便、准确,各项技术指标均满足国内外有关饲料中瘦肉精检测要求,可用于饲料中盐酸克伦特罗、莱克多巴胺、沙丁胺醇和苯乙醇胺A残留的分析测定。 A new method was developed for the determination of clenbuterol, ractopamine, salbuterol and phenylethanolamine A by ultra-performance liquid chromatography-electrospray ionization tandem mass spectrometry. Sample preparation and HPLC-MS/MS analytical conditions were examined and optimized critically by use of a series of experiments study. Samples were extracted by acetonitrile, then cleaned up, and analyzed qualitatively and quantitatively by LC-ESI-MS / MS. The method detection limit ( LOD ) was 0.05 mg / kg. Element concentration was linear with peak area in the range of 0.001-0.2 mg/kg ( r 〉 0.99 ). The average recoveries ranged from 61% to 75%. The method is simple, efficient, accurate and can meet the requirements of determination for clenbuterol, ractopamine, salbuterol and phenylethanolamine A in feeds.
作者 顾亮 丁磊
出处 《化学分析计量》 CAS 2012年第1期37-39,共3页 Chemical Analysis And Meterage
关键词 盐酸克伦特罗 莱克多巴胺 沙丁胺醇 苯乙醇胺A 高效液相色谱-串联质谱 饲料 clenbuterol ractopamine salbuterol phenylethanolamine A liquid chromatography-electrospray ionization tandem mass spectrometry feed
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  • 1Yang Y T, Ecellgott Ma.Multiple action of adrenergic agonistsonskeletal muscle and adipose tissue[J]. Biochemistry, 2000,261:1-10.
  • 2Li Junsuo, Qiu Yueming, Wang Chao. Residue analysis for veterinary drug[M].Shanghai : Shanghai Scientific & Technical Publishers, 2002:641q558.
  • 3高燕红,吴西梅.液质联用快速测定饲料中的莱克多巴胺和克伦特罗[J].中国卫生检验杂志,2005,15(6):643-645. 被引量:20

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