Journal
BIOSENSORS-BASEL
Volume 12, Issue 5, Pages -Publisher
MDPI
DOI: 10.3390/bios12050338
Keywords
quinclorac; enzyme-linked immunoassay; time-resolved fluoroimmunoassay; residue analysis
Funding
- National Natural Science Foundation of China [31801646]
- Science and Technology Project ofNanping Tobacco Company [2021350700240076]
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In this study, ELISA and TRFIA methods were established for the detection and monitoring of quinclorac residue in the environment. The results of both methods were consistent with those of the referenced UPLC-MS/MS method, and they showed good detection performance that met the requirements of quinclorac quantitative determination.
As a common herbicide in farmland, there has been wide concern over quinclorac residue because of its potential risks to the environment and human health. For the detection and monitoring of quinclorac residue in the environment, enzyme-linked immunoassay (ELISA) and time-resolved fluoroimmunoassay (TRFIA) were established. The half-maximal inhibition concentrations (IC50) of ELISA and TRFIA were 0.169 mg/L and 0.087 mg/L with a linear range (IC20 -IC80) of 0.020-1.389 mg/L and 0.004-1.861 mg/L, respectively. Compared with ELISA, the limit of detection (LOD, IC20) and IC50 of TRFIA improved approximately 5-fold and 2-fold. The cross-reaction rates for the quinclorac analogs were less than 2%. The average recoveries of quinclorac in river water, paddy water, paddy soil, and brown rice samples were 77.3-106.1%, with RSDs of 1.7-12.5%. More importantly, the results of the two methods were consistent with that of the referenced method of UPLC-MS/MS (R-2 > 0.98). ELISA and TRFIA both showed good detection performance and could meet the requirements of the quantitative determination of quinclorac. Therefore, the proposed ELISA and TRFIA could be applied to the rapid and sensitive detection and monitoring of quinclorac residue in the environment.
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