节点文献

液相色谱-串联质谱法检测水产品中硝基呋喃类代谢物

Determination of metabolites of nitrofuran antibiotics in aquatic products by high-performance liquid chromatography-tandem mass spectrometry

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 王璟杨楠赵晶权伍英杨军

【Author】 Wang Jing1,Yang Nan2,Zhao Jing1,Quan Wu-ying1,Yang Jun3 (1.Shenyang Center for Disease Control and Prevention,Shenyang 110031,China;2.Shenyang Center for Health Inspection and Supervision,Shenyang 110014,China;3.China Medical University,Shenyang 110005,China)

【机构】 沈阳市疾病预防控制中心沈阳市卫生监督所中国医科大学 沈阳110031沈阳110014沈阳110031沈阳110005

【摘要】 目的:建立硝基呋喃类药物(呋喃唑酮、呋喃它酮、呋喃西林和呋喃妥因)代谢物的液相色谱-串联质谱分析方法。方法:硝基呋喃类代谢物经过二硝基苯甲醛衍生化,用乙酸乙酯提取后经液相色谱分离,电喷雾串联质谱法进行检测。结果:4种硝基呋喃代谢物的定量线性范围均为1~50 ng/ml,线性关系良好(r>0.99),水产品中的定量检测限均为0.5μg/kg,回收率在88.0%~94.3%范围内,相对标准偏差在10.4%以下。结论:本法专属性强,灵敏度和准确度高,可作为分析水产品中硝基呋喃类代谢物残留量的有效手段。

【Abstract】 Objective:To develop a LC-MS/MS method for the simultaneous determination of the metabolites of four nitrofuran antibacterial agents,furazolidone,furaltadone,nitrofurazone and nitrofurantoin in aquatic products.Methods:Samples were derivatised with 2-nitrobenzaldehyde and extracted by ethyl acetate.The analytes were separated and detected by tandem mass spectrometry with electrospray ionization source.Results:The limits of quantification for four nitrofuran metabolites in samples were 0.5 μg/kg.The matrix-matched calibration curve showed good linearity(r2>0.99) in the range of 1~50 ng/ml,The mean recovery was between 88.0% and 94.3% and the relative standard derivations less than 10.4%.Conclusion:This method is specific,sensitive and accurate.It is reliable to determine the nitrofuran metabolites in aquatic products.

  • 【文献出处】 中国卫生检验杂志 ,Chinese Journal of Health Laboratory Technology , 编辑部邮箱 ,2008年06期
  • 【分类号】TS254.7
  • 【被引频次】20
  • 【下载频次】438
节点文献中: 

本文链接的文献网络图示:

本文的引文网络