Study on the Enantioselective Separation, Dissipation, and Residue of Chiral Fenpropathrin in Vegetables by Supercritical Fluid Chromatography-Tandem Mass Spectrometry (SFC-MS/MS).

J Agric Food Chem

State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, P. R. China

Published: December 2024


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Article Abstract

Chiral fenpropathrin is a widely used pyrethroid insecticide. A fast supercritical fluid chromatography-tandem mass spectrometry (SFC-MS/MS) method was developed for the enantioselective study of fenpropathrin in five kinds of vegetables. The enantioseparation could be completed in 2 min, and the recoveries were 75.5-107.7% with RSDs of ≤15.2%. The dissipation half-lives of -fenpropathrin and -fenpropathrin were 2.32-3.62 days and 1.89-3.56 days, respectively. The dissipation of fenpropathrin was the fastest in cucumbers and the slowest in celery cabbage. -Fenpropathrin was preferentially dissipated in celery and cucumber, which was opposite in lettuce and pakchoi. The final residues of -fenpropathrin in celery cabbage, pakchoi, and lettuce were a little above the European Union's maximum residue limits (MRLs) but less than the China's MRLs. The acute and chronic dietary intake risks of -fenpropathrin for all age groups were acceptable. The results would provide a basis for the rational application and risk assessment of fenpropathrin.

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http://dx.doi.org/10.1021/acs.jafc.4c09160DOI Listing

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Study on the Enantioselective Separation, Dissipation, and Residue of Chiral Fenpropathrin in Vegetables by Supercritical Fluid Chromatography-Tandem Mass Spectrometry (SFC-MS/MS).

J Agric Food Chem

December 2024

State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products/Key Laboratory of Detection for Pesticide Residues and Control of Zhejiang, Institute of Agro-product Safety and Nutrition, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, P. R. China

Article Synopsis
  • Chiral fenpropathrin is a common pyrethroid insecticide, and a quick SFC-MS/MS method was created to study its enantioselectivity in five vegetable types.
  • The enantioseparation took just 2 minutes, showing good recovery rates and low variability.
  • The insecticide dissipated fastest in cucumbers and slowest in celery cabbage, with some final residues exceeding EU limits but remaining under China’s, while overall dietary risks for all ages were found to be acceptable.
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Article Synopsis
  • * The process involves extracting samples with acetonitrile, purifying them with a solid-phase extraction column, and using a chiral column for separation under specific conditions, detected by an ultraviolet detector.
  • * The method shows high reliability with low limits of quantification (0.2 mg/kg), excellent recovery rates (80.6-105%), and a good correlation for linearity, making it effective and environmentally friendly for testing food purity.
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Article Synopsis
  • Eight chiral pesticides were studied to assess their stability in various organic solvents and water, with five showing stability across all conditions.
  • Significant racemization (the process of converting one chiral form into its mirror image) occurred for malathion, phenthoate, and fenpropathrin in specific solvents like methanol and ethanol, influenced by temperature and pH levels.
  • The study highlights the role of solvent and pH on the racemization of these pesticides, providing insights into the environmental impact and handling of enantiopure pesticide products.
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Fenpropathrin and fenvalerate are two widely used pyrethroid insecticides. Due to one and two asymmetrical centers, fenpropathrin and fenvalerate consist of two and four stereoisomers, respectively. In the present study, the degradation of fenpropathrin and fenvalerate in two soils, an alkaline soil and an acidic soil, was investigated using enantioselective high-performance liquid chromatography (HPLC) and the following results were obtained.

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A novel chiral stationary phase (CSP) for HPLC was prepared by bonding (R)-1-phenyl-2-(4-methylphenyl)ethylamine amide derivative of (S)-valine to aminopropyl silica gel through a 2-amino-3,5-dinitro-1-carboxamido-benzene unit. The CSP was used for the separation of some amino acid derivatives and pyrethroid insecticides by chiral HPLC. Satisfactory baseline separation required optimization of the variables of mobile phase composition.

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