Foods of plant origin - Multimethod for the determination of pesticide residues in vegetable oils by LC-MS/MS (QuOil)

2019 ◽  
1981 ◽  
Vol 64 (3) ◽  
pp. 743-748 ◽  
Author(s):  
Árpád Ambrus ◽  
Éva Hargitai ◽  
Gabriella Károly ◽  
András Fülöp Ambrus ◽  
János Lantos Ambrus

Abstract o-Tolidine plus KI, p-nitrobenzene-diazoniumfluoroborate, bioassay with fungi and enzyme sources, AgNO3 plus UV radiation, and p-dimethyl-aminobenzaldehyde modes of detection have been selected for TLC screening of pesticide residues in extracts of samples of unknown origin. Single solvents were used for the elution. Coefficients of variation of Rf values were studied as a function of Rf and eluants. Indicator compounds were used for controlling the proper conditions of detection. The detectability of 188 pesticide compounds was tested, and the minimum detectable amounts were determined.


1995 ◽  
Vol 78 (2) ◽  
pp. 431-436 ◽  
Author(s):  
Allesia M Gillespie ◽  
Sean L Daly ◽  
Dalia M Gilvydis ◽  
Felix Schneider ◽  
Stephen M Walters

Abstract Diatomaceous earth columns used with reversed and normal solid phase extraction (SPE) cartridges were evaluated for the quantitative determination of a number of organophosphorus (OP) and organochlorine (OC) pesticide residues in edible vegetable oils and butterfat. An oil or fat sample (about 2 g) in hexane was passed through a diatomaceous earth (Extrelut QE) column and a Cis bonded silica (ODS) SPE cartridge, resulting in the separation of the pesticides from about 98% of the lipids. The eluate was split in half, with the first portion concentrated into acetone for the determination of OP pesticides by gas chromatography with flame photometric detection (GC–FPD). The other half was passed through an Alumina-N SPE cartridge for additional cleanup of lipid matrix to determine OC pesticides by GC with electron-capture detection (GC–ECD). Average recoveries from fortified samples were greater than 89% for the pesticides studied.


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