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Pesticide screening LC-QTOF, Agilent
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National Food Institute, Technical University of Denmark Disposition National Food Institute –EURL –NRL –Personale og udstyr Kolibri Agilent LC-QTOF Bruker LC-QTOF Background – pesticide analysis –Number of pesticides –Quantitative analysis – LC-MS/MS –Pesticide screening Construction of Library Development of method
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National Food Institute, Technical University of Denmark Pesticides Pesticide manual: 1436 pesticides –Metabolites –Isomers PCDL library of Agilent: 1664 pesticides including relevant metabolites Our library: 1716 pesticides including relevant metabolites – retention times of around 1/3 of these
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National Food Institute, Technical University of Denmark Pesticides in our laboratory Number of pesticides introduced to the LC-QTOFQuantitative method: 311 PesticidesQualitative method: 680 pesticides
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National Food Institute, Technical University of Denmark Disposition Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Disposition Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Disposition Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Disposition Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Disposition Screening analysis Library LC- QTOF analysis Validation
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National Food Institute, Technical University of Denmark Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark PCD – CSV file
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National Food Institute, Technical University of Denmark Formula – database - generator
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National Food Institute, Technical University of Denmark PCDL - library
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National Food Institute, Technical University of Denmark PCDL – library - spectra
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National Food Institute, Technical University of Denmark PCDL – library - spectra
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National Food Institute, Technical University of Denmark Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Pesticide screening Eluent A: 0.1% formic acid + 5 mM ammonia in water Eluent B: 0.1% formic acid in acetonitrile Analysis time: 20 min Full scan - m/z = 50-1000 In positive and negative mode
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National Food Institute, Technical University of Denmark Overview on MS Analysis
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National Food Institute, Technical University of Denmark No selection QTOF-analysis – MS scan No collision Used to determine retention time
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National Food Institute, Technical University of Denmark Selection of single mass QTOF-analysis – Targeted MS/MS Collision 10, 20 and 40 V Obtaining compound spectra for Library Spectra of daughter ions from the single ion isolated in the quadropole
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National Food Institute, Technical University of Denmark No selection QTOF-analysis – MS scan with collision Collision 10, 20 and 40 V Screening samples Spectra of daughter ions of all compounds eluting on a certain time point
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National Food Institute, Technical University of Denmark Chromatogram - TIC
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National Food Institute, Technical University of Denmark Spectra – MSscan incl. collision 0V 10V 20V 40V Ofurace, [M+H] +
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National Food Institute, Technical University of Denmark Screening analysis Library LC- QTOF analysis
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search
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National Food Institute, Technical University of Denmark Library Search - result
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National Food Institute, Technical University of Denmark Screening analysis Library LC- QTOF analysis Validation
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National Food Institute, Technical University of Denmark Qualitative versus Quantitative Screening methodConfirmatory method Qualitative (detectability)Quantitative (RSD) No full identification (selectivity)Unambiguous identification Result = + or –Result = value ± SD Automated MS-based methods using accurate mass instruments such ToFs Bioassays – now seldom used
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National Food Institute, Technical University of Denmark Validation – screening method Requirement: Confidence in detection/identification of an analyte at a certain concentration has to be established Need to establish the lowest level of an analyte can be detected in 95% of samples (false negative rate of 5% is acceptable) No requirements with regard to linearity or recovery Exclude false positive results by analysing unspiked (‘blank’) samples.
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National Food Institute, Technical University of Denmark Validation – screening method Analyse 20 different samples for each commodity group spiked at the anticipated screening reporing level (SRL) Samples should cover multiple matrices from the commodity with a minimum of 2 samples per matrix group. Once applied routinely, on-going QC data should be acquired. For any new analyte further validation is required in order to be able to specify the Screening Detection Limit (SDL)
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National Food Institute, Technical University of Denmark Considerations of validation setup How many different samples? –Can we make 2 samples of one apple? –Or do we need to purchase two apples? We have a wish to validate at 3 levels –This is many samples to clean up –Can we then spike after Clean up? No control of recovery!
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National Food Institute, Technical University of Denmark Alternative validation plan 20 blank samples are cleaned up 20 samples spiked at 0.10 mg/kg are cleaned up a A b B, … t T 0.10 µg/mlBlank 0.10 µg/ml500 µl0 µl 0.05 µg/ml500 µl 0.01 µg/ml100 µl900 µl Blank0 µl500 µl The spiked samples are then diluted with the blank samples
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National Food Institute, Technical University of Denmark
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