This paper describes the extension and re-validation of a previously published multi-residue method to currently 140 pesticides and 4 pesticide degradation products in cereals and feedingstuffs. The pesticides were extracted using buffered QuEChERS ("quick, easy, cheap, rugged, effective and safe") method and then cleaned up using dispersive solid-phase extraction with Bondesil PSA and C18 sorbents, and optionally by a freezing-out clean-up step. The final extracts were analyzed in a single injection gas chromatographic-tandem quadrupole mass spectrometric (GC-MS/MS) acquisition method. A high degree of confidence was achieved by entering two multiple reaction monitoring transitions per compound. In this way, quantification of analytical results and unequivocal identification of pesticide residues in compliance with the recent European Union criteria could be done in a single analysis. Thorough optimization of the GC-MS/MS acquisition conditions and application of an effective clean-up procedure has resulted in a remarkable enhancement of the validation parameters. The linearity of the calibration curves was excellent in matrix-matched standards, and yielded the coefficients of determination (R(2))> or =0.99 for approximately 96% of the target analytes. Average recoveries of the pesticides spiked at 0.01mgkg(-1) into a feed mixture and wheat grain were in the range 70-120% with associated RSD values < or =20% for approximately 60% and 67% of the compounds, respectively. At the higher spiking levels of 0.05, 0.1 and 0.5mgkg(-1) average recoveries and RSDs readily met the validation criteria for nearly all the studied pesticides. Based on these results, the proposed approach has been proven to be highly efficient and suitable for routine determinations of multi-class pesticides in a range of cereal and related matrices. Up to now, 145 samples of matrices of differing complexity including cereals grain, bran, whole ears, straw, hay, feed mixtures and other samples such as malt, starch and dry vegetables have been analyzed. A total of 15 different pesticides have been detected, among which pirimiphos methyl (19 cases), deltamethrin (14 cases), tolylfluanid (5 cases), dichlofluanid (5 cases), and tebuconazole (4 cases) were the most frequently encountered ones.
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http://dx.doi.org/10.1016/j.chroma.2008.08.068 | DOI Listing |
J Chromatogr A
January 2025
Environmental & Food Safety Research group of the University of Valencia (SAMA-UV), Desertification Research Centre CIDE (CSIC-UV-GV), Road CV-315 Km 10.7, 46113, Moncada, Valencia, Spain.
Microfibres released from textiles are one of the most common types of microplastics (MPs) found in the environment. Whether they are synthetic or natural, they can undergo degradation in different environmental matrices. This may result in the leaching of a variety of chemicals, mainly textile dyes and additives of high toxicity that need to be regulated.
View Article and Find Full Text PDFJ Environ Sci Health B
January 2025
Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Kafrelsheikh University, Kafrelsheikh, Egypt.
Animal feed significantly influences the content and quality of animal products consumed by humans and plays a crucial role in the food chain. To simultaneously analyze 345 pesticide residues in poultry feed, a modified Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method was developed, utilizing gas chromatography-tandem mass spectrometry (GC-MS/MS). Validation studies were conducted with spiked pesticide standards, and commercial poultry feed samples were analyzed.
View Article and Find Full Text PDFSci Total Environ
January 2025
Human Biomonitoring Research Unit, Department of Precision Health - Luxembourg Institute of Health, 1 A-B rue Thomas Edison, 1445 Strassen, Luxembourg. Electronic address:
While biomonitoring approaches are frequently employed for assessing chemical exposure, many of them are constrained to a limited number of target chemicals, running counter to our current understanding of interactions within chemical mixtures and the growing evidence of multiple exposures within human populations. Although authors agree on the need for more comprehensive methodologies, literature provides insufficient evidence of the multifaceted nature of exposure and of the benefit of widening the analytical scope to improve exposure assessment. Moreover, although multiple exposures are generally admitted, very few are known on the scale of the human chemical exposome.
View Article and Find Full Text PDFJ Chromatogr A
December 2024
Department of Organic and Macromolecular Chemistry, Ghent University, Ghent, 9000, Belgium. Electronic address:
Accurate monitoring of pesticide residues at minimal concentrations is imperative for adherence to stringent regulatory standards in numerous countries. This study presents an innovative methodology employing comprehensive two-dimensional liquid chromatography coupled with high-resolution mass spectrometry (LC × LC-HRMS). The approach ensures high sensitivity and selectivity in detecting targeted compounds.
View Article and Find Full Text PDFJ Chromatogr A
December 2024
Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, 414006, PR China. Electronic address:
At present, the matrix interference in traditional Chinese medicine (TCM) is still a great challenge for multi-residue pesticides analysis. Herein, an alcohol/salt aqueous two-phase system (ATPS) based on n-propanol and (NH)SO was developed by comparing the binodal curve phase diagrams and the extraction rates of pesticides. The specific extraction conditions, including the composition of the ATPS, temperature, pH, and extraction time were explored through single factor experiments, and subsequently optimized using orthogonal array design and response surface methodology.
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