Residue detection and correlation analysis of multiple neonicotinoid insecticides and their metabolites in edible herbs.

Food Chem X

Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100193, China.

Published: March 2023

AI Article Synopsis

  • A green analytical method was developed for extracting and detecting 20 analytes, including 10 neonicotinoid insecticides and their main toxic metabolites, in edible herbs.
  • The study utilized QuEChERS and LC-MS/MS, finding residues in 109 herbal samples, with 90 testing positive and total insecticide residues ranging from 0.26 to 139.28 μg/kg.
  • Acetamiprid and imidacloprid, along with their metabolites, were the most frequently detected, indicating a need for increased awareness of neonicotinoid insecticide residues in edible herbs.

Article Abstract

In this work, a green analytical method was established for the simultaneous extraction and detection of 20 analytes-10 neonicotinoid insecticides and their 10 major toxic metabolites in edible herbs. QuEChERS and LC-MS/MS were used to analyze the 20 analytes in five edible herbs. The residues of the 20 neonicotinoid insecticides and their metabolites in 109 herbal samples were detected, of which 90 samples were positive, and the residue of total neonicotinoid insecticides ranged from 0.26 to 139.28 μg/kg. Acetamiprid (77.06 %, ≤85.95 μg/kg), imidacloprid (67.89 %, ≤32.49 μg/kg) and their metabolites (-desmethyl-acetamiprid (44.04 %, ≤18.42 μg/kg) and desnitro imidacloprid (48.62 %, ≤16.55 μg/kg) were most frequently detected in herbs. Significant positive correlations were found between imidacloprid/acetamiprid and their metabolites in and . Therefore, more attention may be given to the neonicotinoid insecticide residues in edible herbs in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039228PMC
http://dx.doi.org/10.1016/j.fochx.2023.100603DOI Listing

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