Discovery of multiple bee-hazardous pesticides in ornamental plants via the Bee-Plex multi-target microsphere screening method

Exposure to pesticides is one of the main drivers of global bee decline. However, the occurrence of pesticides in bee-attracting crops remains underexposed due to the lack of efficient on-site screening approaches for multi-analyte monitoring. Utilizing color-encoded superparamagnetic microspheres,...

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Veröffentlicht in:Journal of hazardous materials 2025-01, Vol.482, p.136556, Article 136556
Hauptverfasser: Zou, Rubing, van Dam, Ruud, Smits, Nathalie, Beij, Erik, Bovee, Toine, de Graaf, Dirk C., Guo, Yirong, Peters, Jeroen
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container_issue
container_start_page 136556
container_title Journal of hazardous materials
container_volume 482
creator Zou, Rubing
van Dam, Ruud
Smits, Nathalie
Beij, Erik
Bovee, Toine
de Graaf, Dirk C.
Guo, Yirong
Peters, Jeroen
description Exposure to pesticides is one of the main drivers of global bee decline. However, the occurrence of pesticides in bee-attracting crops remains underexposed due to the lack of efficient on-site screening approaches for multi-analyte monitoring. Utilizing color-encoded superparamagnetic microspheres, we constructed a portable 8-plex indirect competitive microsphere-based immunoassay for the simultaneous determination of multiple bee-hazardous residues (Bee-Plex). Through a single measurement within 40 min, Bee-Plex exhibited high sensitivities with IC50values of 0.04, 0.08, 0.14, 0.15, 0.78, 0.86, 7.72, and 8.79 ng/mL for imidacloprid, parathion, fipronil, emamectin, carbofuran, chlorpyrifos, fenpropathrin and carbaryl, respectively. Moreover, the implementation of multiple broad-specific antibodies enables a wide-range screening profile for 30 pesticides and pesticide metabolites, detecting 6 neonicotinoids, 6 N-methyl carbamates 6 organophosphates, 5 avermectins, 5 pyrethroids and 2 phenylpyrazoles. The combination of Bee-Plex screening (93 % accuracy) and LC-MS/MS confirmatory analysis revealed contaminations of neonicotinoids (100 %) and avermectins (70 %) in roses, with occurrence frequencies of 79 %, 79 %, 21 %, 21 %, 7 %, and 7 % for imidacloprid, acetamiprid, clothianidin, thiacloprid, imidaclothiz, and nitenpyram, respectively. Above all, this study offers a powerful analytical tool for rapid screening of multiple bee-hazardous pesticides, offering new insights in the occurrence of multi-pesticide contamination in ornamental plants. [Display omitted] •A sensitive 8-plex immunoassay for multiple bee-hazardous pesticides (Bee-Plex) was established.•The Bee-Plex is able to monitoring all 30 pesticides or metabolites by using broad-specific antibodies.•The LC-MS/MS outcomes confirmed 93 % accuracy for the Bee-Plex screening.•High contaminations of neonicotinoids (100 %) and avermectins (70 %) were found in roses.
doi_str_mv 10.1016/j.jhazmat.2024.136556
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However, the occurrence of pesticides in bee-attracting crops remains underexposed due to the lack of efficient on-site screening approaches for multi-analyte monitoring. Utilizing color-encoded superparamagnetic microspheres, we constructed a portable 8-plex indirect competitive microsphere-based immunoassay for the simultaneous determination of multiple bee-hazardous residues (Bee-Plex). Through a single measurement within 40 min, Bee-Plex exhibited high sensitivities with IC50values of 0.04, 0.08, 0.14, 0.15, 0.78, 0.86, 7.72, and 8.79 ng/mL for imidacloprid, parathion, fipronil, emamectin, carbofuran, chlorpyrifos, fenpropathrin and carbaryl, respectively. Moreover, the implementation of multiple broad-specific antibodies enables a wide-range screening profile for 30 pesticides and pesticide metabolites, detecting 6 neonicotinoids, 6 N-methyl carbamates 6 organophosphates, 5 avermectins, 5 pyrethroids and 2 phenylpyrazoles. The combination of Bee-Plex screening (93 % accuracy) and LC-MS/MS confirmatory analysis revealed contaminations of neonicotinoids (100 %) and avermectins (70 %) in roses, with occurrence frequencies of 79 %, 79 %, 21 %, 21 %, 7 %, and 7 % for imidacloprid, acetamiprid, clothianidin, thiacloprid, imidaclothiz, and nitenpyram, respectively. Above all, this study offers a powerful analytical tool for rapid screening of multiple bee-hazardous pesticides, offering new insights in the occurrence of multi-pesticide contamination in ornamental plants. 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However, the occurrence of pesticides in bee-attracting crops remains underexposed due to the lack of efficient on-site screening approaches for multi-analyte monitoring. Utilizing color-encoded superparamagnetic microspheres, we constructed a portable 8-plex indirect competitive microsphere-based immunoassay for the simultaneous determination of multiple bee-hazardous residues (Bee-Plex). Through a single measurement within 40 min, Bee-Plex exhibited high sensitivities with IC50values of 0.04, 0.08, 0.14, 0.15, 0.78, 0.86, 7.72, and 8.79 ng/mL for imidacloprid, parathion, fipronil, emamectin, carbofuran, chlorpyrifos, fenpropathrin and carbaryl, respectively. Moreover, the implementation of multiple broad-specific antibodies enables a wide-range screening profile for 30 pesticides and pesticide metabolites, detecting 6 neonicotinoids, 6 N-methyl carbamates 6 organophosphates, 5 avermectins, 5 pyrethroids and 2 phenylpyrazoles. The combination of Bee-Plex screening (93 % accuracy) and LC-MS/MS confirmatory analysis revealed contaminations of neonicotinoids (100 %) and avermectins (70 %) in roses, with occurrence frequencies of 79 %, 79 %, 21 %, 21 %, 7 %, and 7 % for imidacloprid, acetamiprid, clothianidin, thiacloprid, imidaclothiz, and nitenpyram, respectively. Above all, this study offers a powerful analytical tool for rapid screening of multiple bee-hazardous pesticides, offering new insights in the occurrence of multi-pesticide contamination in ornamental plants. 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source Elsevier ScienceDirect Journals
subjects Bee-hazardous pesticides
LC-MS/MS
Microsphere-based immunoassay
Multi-analyte detection
Ornamental plants
title Discovery of multiple bee-hazardous pesticides in ornamental plants via the Bee-Plex multi-target microsphere screening method
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