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机构地区:[1]山东出入境检验检疫局技术中心,青岛266002 [2]青岛大学化学化工学院,青岛266071
出 处:《分析试验室》2014年第1期48-53,共6页Chinese Journal of Analysis Laboratory
基 金:国家质检总局科技计划项目(2011IK222)资助
摘 要:建立了凝胶渗透色谱(GPC)净化、气相色谱.串联质谱(GC—MS/MS)同时测定植物油中15种欧盟优控多环芳烃(PAHs)残留的分析方法。植物油样品加入同位素内标混合溶液后经乙腈一丙酮(体积比为60:40)混合提取、GPC净化,GC—MS/MS采用选择反应监测模式(SRM)采集数据后进行定性/定量分析;优化了影响分析结果的仪器条件。采用内标法定量,植物油样品中添加回收率在70.3%~123.5%之间,相对标准偏差为1.5%-9.9%,定量限为0.276~0.436μg/kg,相关系数均大于O.9985。An efficient and selective analytical method for the determination and the quantification of 15 EU pri- ority polycyclic aromatic hydrocarbons (PAHs) in vegetable oil has been developed. The samples were extracted by acetonitrile/acetone (V: V=60:40) followed by a purification with gel permeation chromatography (GPC). Identification and quantification were performed using GC-MS/MS with selected reaction monitoring (SRM) mode, with an isotope dilution approach. The novel combination of selective extraction followed by purification provides highly purified analytes combined to a fast and automated method. Recoveries were between 70. 3 % and 123.5%. Relative standard deviations were between 1.5% and 9. 9%. Limits of detection were between 0. 276 -0. 436 μg/kg.
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