李晋津,李辉,邵辉,刘磊,李娜,宋淑荣,郭永泽,张玉婷,陈秋生.QuEChERS-超高效液相色谱-串联质谱法测定山葵中乐果的残留量[J].食品安全质量检测学报,2018,9(17):4503-4507
QuEChERS-超高效液相色谱-串联质谱法测定山葵中乐果的残留量
Determination of dimethoate residues in horseradish by quechers-ultra performance liquid chromatography-tandem mass spectrometry
投稿时间:2018-07-05  修订日期:2018-09-01
DOI:
中文关键词:  乐果  山葵  QuEChERS方法  超高效液相色谱-串联质谱法
英文关键词:dimethoate  horseradish  quechers method  ultra performance liquid chromatography-tandem mass spectrometry
基金项目:国家重点研发计划子课题(2016YFD080100703)、天津市蔬菜产业体系创新团队(ITTVRS2017021)、天津市重点研发计划项目(17YFXTZC00040)、天津市农业科学院院长基金项目(16002)
作者单位
李晋津 天津市农业质量标准与检测技术研究所 
李辉 天津市农业质量标准与检测技术研究所 
邵辉 天津市农业质量标准与检测技术研究所 
刘磊 天津市农业质量标准与检测技术研究所 
李娜 天津市农业质量标准与检测技术研究所 
宋淑荣 天津市农业质量标准与检测技术研究所 
郭永泽 天津市农业质量标准与检测技术研究所 
张玉婷 天津市农业质量标准与检测技术研究所 
陈秋生 天津市农业质量标准与检测技术研究所 
AuthorInstitution
LI Jin-Jin Tianjin Institute of Agricultural Quality Standard and Testing Technology 
LI Hui Tianjin Institute of Agricultural Quality Standard and Testing Technology 
SHAO Hui Tianjin Institute of Agricultural Quality Standard and Testing Technology 
LIU Lei Tianjin Institute of Agricultural Quality Standard and Testing Technology 
LI Na Tianjin Institute of Agricultural Quality Standard and Testing Technology 
SONG Shu-Rong Tianjin Institute of Agricultural Quality Standard and Testing Technology 
GUO Yong-Ze Tianjin Institute of Agricultural Quality Standard and Testing Technology 
ZHANG Yu-Ting Tianjin Institute of Agricultural Quality Standard and Testing Technology 
Chen Qiu-sheng Tianjin Institute of Agricultural Quality Standard and Testing Technology 
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中文摘要:
      目的 建立QuEChERS-超高效液相色谱-串联质谱法测定山葵中乐果残留量的分析方法。方法 山葵样品用乙腈和水提取, 盐析后取上清液, 上清液经C18、PSA、无水MgSO4净化, 在电喷雾正离子(electronic spray ion, ESI+)模式下, 通过优化色谱分离条件, 用超高效液相色谱-串联质谱法采用多反应监测(multiple reaction monitoring, MRM)模式检测, 结合乐果标准曲线进行外标法定量。结果 方法中乐果在0.00125~ 0.5 mg/L浓度范围内线性关系良好, 线性方程为Y=2371831.1X+10169.6, 相关系数r=0.9998(n=6)。山葵中乐果在0.01、0.1、2 mg/kg 3个添加浓度水平下, 平均回收率88.1%~97.8%, 相对标准偏差为1.0%~3.5%(n=5)。该方法乐果在山葵中定量限为0.01 mg/kg。结论 所建立的分析方法操作简便, 分离、净化效果良好, 灵敏度、准确度和精密度符合农药残留检测要求, 可用于山葵中乐果残留量检测。
英文摘要:
      Objective To establish a method for the determination of dimethoate residues in horseradish by quechers-ultra performance liquid chromatography-tandem mass spectrometry. Methods Horseradish samples were extracted with acetonitrile and water, the supernatant was taken and purified by C18, PSA and anhydrous MgSO4 after salting-out, in the electrospray positive ion (ESI+) mode, by optimizing chromatographic separation conditions, and the multi-reaction monitoring (MRM) mode was used for ultra performance liquid chromatography-tandem mass spectrometry, combined with the dimethoate standard curve to quantify. Results The method has a good linear relationship in the concentration range of 0.00125-0.5 mg/L. The linear equation was Y=2371831.1X+10169.6, and the correlation coefficient (r) was 0.9998 (n=6). The average recoveries of dimethoate were 88.1%-97.8% at the concentrations of 0.01, 0.1 and 2 mg/kg, and the relative standard deviations (RSDs) were 1.0%-3.5% (n=5). The limit of quantitative of the method was 0.01 mg/kg in horseradish. Conclusion The method is simple to operate, effective in separation and purification, and the sensitivity, accuracy and precision can meet the requirements of pesticide residue detection, which can be used for detection of residues in horseradish.
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