Literature DB >> 33364182

Use of a deactivated PTV injector liner and GCMS/MS for the quantitative determination of multiple pesticide residues in fruit and vegetables.

Laura M Melton1, Michael J Taylor1.   

Abstract

The quantitative determination of multiple pesticide residues in food is an iterative process given the frequent changes in monitoring specifications set by regulatory authorities, introduction of new pesticide active ingredients, variety of commodities encountered and advances in the capability of analytical instrumentation and software platforms. The method described here:•replaces our previous methodology [1] that was based on an ethyl acetate extraction [2], two different sample extract clean-up regimes depending on the commodity; either Gel Permeation Chromatography (GPC) or Solid Phase Extraction (SPE) and GC/MSMS analysis using cool on-column injection and permits higher throughput using the same QuEChERS extraction method used for LCMS/MS analysis [3]•uses PTV injection incorporating a deactivated (baffled) injection liner required to improve performance for 'difficult to analyse' pesticides e.g. captan, dichlofluanid, folpet, tolylfluanid.•has been validated for the quantitative determination of 113 different pesticides and their metabolites in a range of fruit and vegetables of high water content and high acid and high water content i.e. cabbage, lemon, pepper, plum and spinach and complies with requirements of European Commission guidance document on Analytical Quality Control and Method Validation Procedures for Pesticides Residues Analysis in food and feed - SANTE/12682/2019 [4]. Crown
Copyright © 2020 Published by Elsevier B.V.

Entities:  

Keywords:  AP, analyte protectants; Captan; DSPE, dispersive solid phase extraction; EU, European union; Folpet; Fruit and vegetables; GC, gas chromatography; GCB, graphitised carbon black; GCMS/MS; GCMS/MS, gas chromatography tandem mass spectrometry; GPC, gel permeation chromatography; ISTD, internal standard; Injector liner; PTV; PTV, programmable temperature vapourising; Pesticide residues; QuEChERS; RL, Reporting Level; SPE, Solid Phase Extraction; SRM, Simultaneous Reaction Monitoring; UK, United Kingdom

Year:  2020        PMID: 33364182      PMCID: PMC7750143          DOI: 10.1016/j.mex.2020.101180

Source DB:  PubMed          Journal:  MethodsX        ISSN: 2215-0161


  2 in total

1.  Analysis of pesticide residues in fruit and vegetables with ethyl acetate extraction using gas and liquid chromatography with tandem mass spectrometric detection.

Authors:  Tuija Pihlström; Gun Blomkvist; Paula Friman; Ulla Pagard; Bengt-Göran Osterdahl
Journal:  Anal Bioanal Chem       Date:  2007-07-04       Impact factor: 4.142

2.  Fast and easy multiresidue method employing acetonitrile extraction/partitioning and "dispersive solid-phase extraction" for the determination of pesticide residues in produce.

Authors:  Michelangelo Anastassiades; Steven J Lehotay; Darinka Stajnbaher; Frank J Schenck
Journal:  J AOAC Int       Date:  2003 Mar-Apr       Impact factor: 1.913

  2 in total
  1 in total

1.  Editorial overview: Virtual collection on chromatographic and mass spectrometric methods in food, health, and agriculture.

Authors:  Andrew J Gravelle
Journal:  MethodsX       Date:  2022-01-28
  1 in total

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