Determination of 167 Pesticide Residues in Animal-originated Foodstuffs by Combined Purification of Gel Permeation Chromatography and Solid-phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry
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Determination of 167 Pesticide Residues in Animal-originated Foodstuffs by Combined Purification of Gel Permeation Chromatography and Solid-phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry
Vol. 34, Issue 6, Pages: 639-645(2015)
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国家食品安全风险评估中心卫生部食品安全风险评估重点实验室
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Determination of 167 Pesticide Residues in Animal-originated Foodstuffs by Combined Purification of Gel Permeation Chromatography and Solid-phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry. [J]. 34(6):639-645(2015)
DOI:
Determination of 167 Pesticide Residues in Animal-originated Foodstuffs by Combined Purification of Gel Permeation Chromatography and Solid-phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry. [J]. 34(6):639-645(2015)DOI:
Determination of 167 Pesticide Residues in Animal-originated Foodstuffs by Combined Purification of Gel Permeation Chromatography and Solid-phase Extraction Coupled with Gas Chromatography-Tandem Mass Spectrometry
A new analytical method was developed for the determination of 167 pesticides in animal-originated foods,including meat and aquatic.The pesticide residues were extracted from animal-originated samples with acetonitrile,and purified by gel permeation chromatography and solid-phase extraction(Carb-NH2).The detection could be achieved by gas chromatography-tandem mass spectrometry(GC-MS/MS),and the quantification was performed using the external standard calibration.The experimental results showed that the linear ranges for 167 pesticides were in the range of 1-200 μg/L with correlation coefficients larger than 0.994.The limits of detection and quantitation for 167 pesticides in the spiked blank pork sample were in the ranges of 0.3-3 μg/kg and 1-10 μg/kg,respectively.The spiked recoveries at levels of 0.01 mg/kg and 0.04 mg/kg using pork samples as blank matrix were in the range of 66.4%-111.5%,and the relative standard deviations(RSDs) were 1.3%-17.8%.The method has the advantages of accuracy,reliability,high sensitivity and efficient cleanup procedure,and could meet the demand for pesticide routine analysis.
关键词
农药多残留气相色谱-串联质谱凝胶渗透色谱固相萃取动物性食品
Keywords
pesticides residuesgas chromatography-tandem mass spectrometry(GC-MS/MS)gel permeation chromatographysolid-phase extractionanimal-originated food
Determination of 43 Persistent Organochlorine Pollutants in Human Serum by Gas Chromatography-Tandem Mass Spectrometry
Determination of Ethoxyquinoline and Ethoxyquinoline Dimer in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of Fipronil and Its Metabolites in Rice Fishing Water Samples by SPE/UPLC-MS/MS
Determination of Bisphenol Compounds in Drinking Water by High Performance Liquid Chromatography with Pipette Tip Solid-phase Extraction Using Carboxylated Multi-walled Carbon Nanotubes as Adsorbent
Determination of Tretoquinol in Pungent Spice by Solid-phase Extraction Coupled Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry
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School of Public Health, Anhui Medical University
National Institute of Environmental Health,Chinese Center for Disease Control and Prevention,China CDC Key Laboratory of Environment and Population Health
College of Food and Pharmaceutical Engineering,Nanjing Normal University
Animal,Plant and Food Inspection Center,Nanjing Customs
Guangdong Provincial Key Laboratory of Aquatic Animal Immunology and Sustainable Aquaculture,Key Laboratory of Prevention and Control for Aquatic Invasive Alien Species,Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute,Chinese Academy of Fishery Sciences