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Research on Rapid Detection Technology for β(2)-Agonists: Multi-Residue Fluorescence Immunochromatography Based on Dimeric Artificial Antigen

To detect two types of β(2)-agonist residues at the same time, we coupled two haptens of clenbuterol (CLE) and ractopamine (RAC) to the same carrier protein through diazotization to prepare dimeric artificial antigen, and a fluorescent lateral flow immunoassay method based on europium nanoparticles...

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Detalles Bibliográficos
Autores principales: Liu, Miaomiao, Ma, Biao, Wang, Yaping, Chen, Erjing, Li, Jiali, Zhang, Mingzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949518/
https://www.ncbi.nlm.nih.gov/pubmed/35327285
http://dx.doi.org/10.3390/foods11060863
Descripción
Sumario:To detect two types of β(2)-agonist residues at the same time, we coupled two haptens of clenbuterol (CLE) and ractopamine (RAC) to the same carrier protein through diazotization to prepare dimeric artificial antigen, and a fluorescent lateral flow immunoassay method based on europium nanoparticles (EuNP-FLFIA) was established by combining polyclonal antibodies with europium nanoparticles to form probes. Under optimized conditions, the EuNP-FLFIA could simultaneously detect eight aniline-type and one phenol-type β(2)-agonists, and the limits of detection (LOD) were 0.11–0.19 ng/mL and 0.12 ng/mL, respectively. The recovery rate of this method was 84.00–114.00%. This method was verified by liquid chromatography–tandem mass spectrometry (LC-MS/MS), and the test results were consistent (R(2) > 0.98). Therefore, the method established in this study could be used as a high-throughput screening for the efficient and sensitive detection of β(2)-agonists in food.