Determination of organophosphorus pesticide residues in the liver by gas chromatography with flame photometric detection
Tomasz Kiljanek, Alicja Niewiadowska, S. Semeniuk
Abstract
Tomasz Kiljanek, Alicja Niewiadowska, S. Semeniuk
Abstract
A method for simultaneous determination of residues of six organophosphorus pesticides in animal live r samples has been developed and validated. The method is based on the extraction of organophosphorus pesticides with a m ixture of acetone-petroleum ether, clean up on a gel permeation chromatography, further clean up on a small silica gel column, and finally determination by gas chromatography with flame photometric detection. The recovery, investigated by analysing blank liver s amples spiked with chlorpyrifos-methyl, chlorpyrifos, diazinon, parath ion, and pirimiphos-methyl at levels of 5, 25, 50, and 75 µg/kg, and with chlorfenvinphos at levels of 5, 10, and 15 µg/kg, ranged from 75.6% to 107.5%. Performance characteristics, such as repeatability and within-laboratory reproducibility, expressed as coefficient of variation, were less than 20%, and uncertainty <21%. Linearity ranged between 5 and 1,000 ng/mL. The limits of quantification were 5 µg/kg for all compounds and allowed determination of residues below the MRLs set by the European Union. The satisfactory z-score results of international pr oficiency tests confirmed good accuracy, reproducibility, and reliability of the developed method.
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A method for simultaneous determination of residues of six organophosphorus pesticides in animal live r samples has been developed and validated. The method is based on the extraction of organophosphorus pesticides with a m ixture of acetone-petroleum ether, clean up on a gel permeation chromatography, further clean up on a small silica gel column, and finally determination by gas chromatography with flame photometric detection. The recovery, investigated by analysing blank liver s amples spiked with chlorpyrifos-methyl, chlorpyrifos, diazinon, parath ion, and pirimiphos-methyl at levels of 5, 25, 50, and 75 µg/kg, and with chlorfenvinphos at levels of 5, 10, and 15 µg/kg, ranged from 75.6% to 107.5%. Performance characteristics, such as repeatability and within-laboratory reproducibility, expressed as coefficient of variation, were less than 20%, and uncertainty <21%. Linearity ranged between 5 and 1,000 ng/mL. The limits of quantification were 5 µg/kg for all compounds and allowed determination of residues below the MRLs set by the European Union. The satisfactory z-score results of international pr oficiency tests confirmed good accuracy, reproducibility, and reliability of the developed method.
Key concepts: Chromatography, Repeatability, Reproducibility, Chemistry, Diazinon, Gas chromatography, Pesticide residue, Pesticide