Determination of 19 Insecticides,Fungicides and Their Metabolites in Edible Fungi by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersed Solid Phase Extraction
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Determination of 19 Insecticides,Fungicides and Their Metabolites in Edible Fungi by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersed Solid Phase Extraction
Vol. 39, Issue 9, Pages: 1105-1111(2020)
作者机构:
嘉应学院梅州师范分院
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Determination of 19 Insecticides,Fungicides and Their Metabolites in Edible Fungi by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersed Solid Phase Extraction. [J]. 39(9):1105-1111(2020)
DOI:
Determination of 19 Insecticides,Fungicides and Their Metabolites in Edible Fungi by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersed Solid Phase Extraction. [J]. 39(9):1105-1111(2020)DOI:
Determination of 19 Insecticides,Fungicides and Their Metabolites in Edible Fungi by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersed Solid Phase Extraction
An ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) with dispersed solid phase extraction was established for the determination of 19 insecticides,fungicides and their metabolites in edible fungi,including mushrooms,black fungus and tremella,etc.The samples were firstly extracted with acetonitrile by homogeneous oscillation,then purified with PSA and C18,and finally separated on an XR-ODS column(2.0 mm×100 mm×2.2 μm) with acetonitrile and water as mobile phases.The analytes were detected under multi-reaction monitoring(MRM) mode,determined by retention time and ion abundance ratio of the fragments and quantified by the external standard method with matrix-matched standard curves.Under the optimized conditions,19 analytes showed good linearities(r2>0.998 0) in their respective concentration ranges.The limits of detection and limits of quantitation were in the ranges of 0.2-0.6 μg/kg and 0.5-2.0 μg/kg,respectively.Average recoveries for the analytes at three spiked levels ranged from 83.1% to 106% with relative standard deviations(RSD,n=6) of 5.0%-12%.The method was rapid,accurate and sensitive,and was suitable for the determination of insecticides,fungicides and their metabolites in edible fungi.
关键词
超高效液相色谱-串联质谱食用菌农药代谢物分散固相萃取
Keywords
ultra performance liquid chromatography-tandem mass spectrometryedible fungipesticidesmetabolitesdispersed solid phase extraction
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