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Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples

[Image: see text] Algal blooms that contaminate freshwater resources with cyanotoxins constitute, nowadays, a global concern. To deal with this problem, a variety of analytical methods, including immunochemical assays, are available for the main algal toxins, for example, microcystins, nodularins, a...

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Autores principales: Cevallos-Cedeño, Ramón E., Quiñones-Reyes, Guillermo, Agulló, Consuelo, Abad-Somovilla, Antonio, Abad-Fuentes, Antonio, Mercader, Josep V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352146/
https://www.ncbi.nlm.nih.gov/pubmed/35853613
http://dx.doi.org/10.1021/acs.analchem.2c01939
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author Cevallos-Cedeño, Ramón E.
Quiñones-Reyes, Guillermo
Agulló, Consuelo
Abad-Somovilla, Antonio
Abad-Fuentes, Antonio
Mercader, Josep V.
author_facet Cevallos-Cedeño, Ramón E.
Quiñones-Reyes, Guillermo
Agulló, Consuelo
Abad-Somovilla, Antonio
Abad-Fuentes, Antonio
Mercader, Josep V.
author_sort Cevallos-Cedeño, Ramón E.
collection PubMed
description [Image: see text] Algal blooms that contaminate freshwater resources with cyanotoxins constitute, nowadays, a global concern. To deal with this problem, a variety of analytical methods, including immunochemical assays, are available for the main algal toxins, for example, microcystins, nodularins, and saxitoxins, with the remarkable exception of anatoxin-a. Now, for the first time, highly sensitive, enantioselective immunoassays for anatoxin-a have been validated using homemade monoclonal antibodies. Two competitive enzyme-linked immunosorbent assays were developed in different formats, with detection limits for (+)-anatoxin-a of 0.1 ng/mL. Excellent recovery values between 82 and 117%, and coefficients of variation below 20%, were observed using environmental water samples fortified between 0.5 and 500 ng/mL. In addition, a lateral-flow immunochromatographic assay was optimized for visual and instrumental reading of results. This test showed a visual detection limit for (+)-anatoxin-a of 4 ng/mL. Performance with a reader was validated in accordance with the European guidelines for semiquantitative rapid methods for small chemical contaminants. Thus, at a screening target concentration of 2 ng/mL, the probability of a blank sample to be classified as “suspect” was as low as 0.2%. Finally, the optimized direct enzyme immunoassay was validated by comparison with high-performance liquid chromatography-tandem mass spectroscopy data and showed a good correlation (r = 0.995) with a slope of 0.94. Moreover, environmental water samples containing more than 2 ng/mL of anatoxin-a were detected by the developed dipstick assay. These results provide supplementary and complementary strategies for monitoring the presence of anatoxin-a in water.
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spelling pubmed-93521462022-08-05 Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples Cevallos-Cedeño, Ramón E. Quiñones-Reyes, Guillermo Agulló, Consuelo Abad-Somovilla, Antonio Abad-Fuentes, Antonio Mercader, Josep V. Anal Chem [Image: see text] Algal blooms that contaminate freshwater resources with cyanotoxins constitute, nowadays, a global concern. To deal with this problem, a variety of analytical methods, including immunochemical assays, are available for the main algal toxins, for example, microcystins, nodularins, and saxitoxins, with the remarkable exception of anatoxin-a. Now, for the first time, highly sensitive, enantioselective immunoassays for anatoxin-a have been validated using homemade monoclonal antibodies. Two competitive enzyme-linked immunosorbent assays were developed in different formats, with detection limits for (+)-anatoxin-a of 0.1 ng/mL. Excellent recovery values between 82 and 117%, and coefficients of variation below 20%, were observed using environmental water samples fortified between 0.5 and 500 ng/mL. In addition, a lateral-flow immunochromatographic assay was optimized for visual and instrumental reading of results. This test showed a visual detection limit for (+)-anatoxin-a of 4 ng/mL. Performance with a reader was validated in accordance with the European guidelines for semiquantitative rapid methods for small chemical contaminants. Thus, at a screening target concentration of 2 ng/mL, the probability of a blank sample to be classified as “suspect” was as low as 0.2%. Finally, the optimized direct enzyme immunoassay was validated by comparison with high-performance liquid chromatography-tandem mass spectroscopy data and showed a good correlation (r = 0.995) with a slope of 0.94. Moreover, environmental water samples containing more than 2 ng/mL of anatoxin-a were detected by the developed dipstick assay. These results provide supplementary and complementary strategies for monitoring the presence of anatoxin-a in water. American Chemical Society 2022-07-19 2022-08-02 /pmc/articles/PMC9352146/ /pubmed/35853613 http://dx.doi.org/10.1021/acs.analchem.2c01939 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Cevallos-Cedeño, Ramón E.
Quiñones-Reyes, Guillermo
Agulló, Consuelo
Abad-Somovilla, Antonio
Abad-Fuentes, Antonio
Mercader, Josep V.
Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title_full Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title_fullStr Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title_full_unstemmed Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title_short Rapid Immunochemical Methods for Anatoxin-a Monitoring in Environmental Water Samples
title_sort rapid immunochemical methods for anatoxin-a monitoring in environmental water samples
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352146/
https://www.ncbi.nlm.nih.gov/pubmed/35853613
http://dx.doi.org/10.1021/acs.analchem.2c01939
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