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Utilization of a Novel Immunofluorescence Instrument Prototype for the Determination of the Herbicide Glyphosate

Molecules 2022 3 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Eszter Takács, Mária Mörtl, Borbála Gémes, Borbála Gémes, Fanni Szendrei, Fanni Szendrei, Csaba Keszei, Mária Mörtl, Eszter Takács, Csaba Keszei, Attila Barócsi, András Székács Sándor Lenk, András Székács László Domján, András Székács András Székács Mária Mörtl, András Székács

Summary

Researchers developed an enzyme-linked fluorescent immunoassay method using a novel immunofluorescence instrument prototype for quantitative determination of the herbicide glyphosate in environmental matrices including surface water, soil, and plant tissues. The method provided sensitive detection of glyphosate as a ubiquitous agricultural pollutant across aquatic and terrestrial ecosystems.

Body Systems

An enzyme-linked fluorescent immunoassay (ELFIA) method has been developed for the quantitative analytical determination of the herbicide active ingredient glyphosate in environmental matrices (surface water, soil, and plant tissues). Glyphosate, as a ubiquitous agricultural pollutant, is a xenobiotic substance with exposure in aquatic and terrestrial ecosystems due its extremely high worldwide application rate. The immunoassay developed in Project Aquafluosense is part of a fluorescence-based instrumentation setup for the in situ determination of several characteristic water quality parameters. The 96-well microplate-based competitive immunoassay method applies fluorescence signal detection in the concentration range of 0-100 ng/mL glyphosate. Application of the fluorescent signal provides a limit of detection of 0.09 ng/mL, which is 2.5-fold lower than that obtained with a visual absorbance signal. Beside the improved limit of detection, determination by fluorescence provided a wider and steeper dynamic range for glyphosate detection. No matrix effect appeared for the undiluted surface water samples, while plant tissues and soil samples required dilution rates of 1:10 and 1:100, respectively. No cross-reaction was determined with the main metabolite of glyphosate, N-aminomethylphosphonic acid, and related compounds.

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