Rapid Detection of 36 Pesticide Residues in Peanut by Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
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Rapid Detection of 36 Pesticide Residues in Peanut by Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
Vol. 36, Issue 4, Pages: 502-506(2017)
作者机构:
1. 中国农业科学院蔬菜花卉研究所
2. 农业部蔬菜质量安全控制重点实验室
3. 农业部园艺作物生物学与种质创制重点实验室
4. 安捷伦科技(中国)有限公司
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Rapid Detection of 36 Pesticide Residues in Peanut by Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 36(4):502-506(2017)
DOI:
Rapid Detection of 36 Pesticide Residues in Peanut by Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 36(4):502-506(2017)DOI:
Rapid Detection of 36 Pesticide Residues in Peanut by Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
A multiresidue analytical method was developed for the rapid detection of 36 pesticides in peanut using ultra high performance liquid chromatography-tandem mass spectrometric technique(UHPLC-MS/MS).Peanut samples were extracted with acetonitrile,and then cleaned up with QuEChERS EMR-Lipid.The extract was detected by UHPLC-MS/MS.The positive ion mode and multiple reaction monitoring(MRM) mode were used to identify and quantify 36 pesticide residues in peanut.All pesticides had good linearity with correlation coefficients above 0.994.The average recoveries of the 36 pesticides ranged from 70.4% to 119% with relative standard deviations(RSDs) of 1.3%-19.4% at spiked levels of 0.005,0.01,0.10 mg/kg.The quantitation limits of this method were in the range of 0.002 5-0.05 mg/kg. With the advantages of simplicity,rapidness,sensitivity and good purifying effect,the method was suitable for the rapid determination of pesticide residues in peanut.
关键词
农药残留花生脂质去除超高效液相色谱-串联质谱(UHPLC-MS/MS)
Keywords
pesticide residuespeanutenhanced matrix removalultra high performance liquid chromatography-tandem mass spectrometry(UHPLC-MS/MS)
Determination of Pesticide Residues in Peanuts by Gas Chromatography-Tandem Mass Spectrometry Coupled with Magnetic Solid Phase Extraction
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