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Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments

Losartan potassium (LOS) is one of the most antihypertensives used in the world, and its presence in environmental matrices can cause impacts to biota. In this study, the ecotoxicity and genotoxicity of LOS was assessed before and after treatment by UVC/photolysis and UV/H(2)O(2). The photodegradati...

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Autores principales: Adams, Eliane, Neves, Bruno B., Prola, Liziê D. T., de Liz, Marcus V., Martins, Lucia R. R., Ramsdorf, Wanessa A., de Freitas, Adriane M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609376/
https://www.ncbi.nlm.nih.gov/pubmed/33145733
http://dx.doi.org/10.1007/s11356-020-11420-9
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author Adams, Eliane
Neves, Bruno B.
Prola, Liziê D. T.
de Liz, Marcus V.
Martins, Lucia R. R.
Ramsdorf, Wanessa A.
de Freitas, Adriane M.
author_facet Adams, Eliane
Neves, Bruno B.
Prola, Liziê D. T.
de Liz, Marcus V.
Martins, Lucia R. R.
Ramsdorf, Wanessa A.
de Freitas, Adriane M.
author_sort Adams, Eliane
collection PubMed
description Losartan potassium (LOS) is one of the most antihypertensives used in the world, and its presence in environmental matrices can cause impacts to biota. In this study, the ecotoxicity and genotoxicity of LOS was assessed before and after treatment by UVC/photolysis and UV/H(2)O(2). The photodegradations were carried out at LOS solutions (2.5 mg L(−1); 4.6 μM) for 30, 60, 90, 120, 240, and 480 min of treatment. For chromatographic analysis, the samples were submitted to solid-phase extraction (SPE) and analyzed by HPLC-DAD. Ecotoxicity bioassays were conducted using Daphnia magna (acute) and Desmodesmus subspicatus (chronic) for all the degradation times. To evaluate the genotoxicity, the comet assay was performed with a D. magna whole organism cell suspension applying the alkaline gel electrophoresis technique. For both process, the degradation rate was over 99% at 30 min, which reduced the acute toxicity of LOS to D. magna. In addition, only the sample treated at 240 min by UV/H(2)O(2) showed significant chronic and acute toxicity. However, the genotoxicity effect was observed for samples treated LOS before treatment and at 480 min by UV/H(2)O(2). Therefore, even reaching high LOS degradation rates, for both processes, the bioassays demonstrated the importance of ecotoxicological analyses by AOPs treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-020-11420-9.
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spelling pubmed-76093762020-11-05 Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments Adams, Eliane Neves, Bruno B. Prola, Liziê D. T. de Liz, Marcus V. Martins, Lucia R. R. Ramsdorf, Wanessa A. de Freitas, Adriane M. Environ Sci Pollut Res Int Advanced Oxidation/Reduction Technologies: An Perspective from Iberoamerican Countries Losartan potassium (LOS) is one of the most antihypertensives used in the world, and its presence in environmental matrices can cause impacts to biota. In this study, the ecotoxicity and genotoxicity of LOS was assessed before and after treatment by UVC/photolysis and UV/H(2)O(2). The photodegradations were carried out at LOS solutions (2.5 mg L(−1); 4.6 μM) for 30, 60, 90, 120, 240, and 480 min of treatment. For chromatographic analysis, the samples were submitted to solid-phase extraction (SPE) and analyzed by HPLC-DAD. Ecotoxicity bioassays were conducted using Daphnia magna (acute) and Desmodesmus subspicatus (chronic) for all the degradation times. To evaluate the genotoxicity, the comet assay was performed with a D. magna whole organism cell suspension applying the alkaline gel electrophoresis technique. For both process, the degradation rate was over 99% at 30 min, which reduced the acute toxicity of LOS to D. magna. In addition, only the sample treated at 240 min by UV/H(2)O(2) showed significant chronic and acute toxicity. However, the genotoxicity effect was observed for samples treated LOS before treatment and at 480 min by UV/H(2)O(2). Therefore, even reaching high LOS degradation rates, for both processes, the bioassays demonstrated the importance of ecotoxicological analyses by AOPs treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-020-11420-9. Springer Berlin Heidelberg 2020-11-04 2021 /pmc/articles/PMC7609376/ /pubmed/33145733 http://dx.doi.org/10.1007/s11356-020-11420-9 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Advanced Oxidation/Reduction Technologies: An Perspective from Iberoamerican Countries
Adams, Eliane
Neves, Bruno B.
Prola, Liziê D. T.
de Liz, Marcus V.
Martins, Lucia R. R.
Ramsdorf, Wanessa A.
de Freitas, Adriane M.
Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title_full Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title_fullStr Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title_full_unstemmed Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title_short Ecotoxicity and genotoxicity assessment of losartan after UV/H(2)O(2) and UVC/photolysis treatments
title_sort ecotoxicity and genotoxicity assessment of losartan after uv/h(2)o(2) and uvc/photolysis treatments
topic Advanced Oxidation/Reduction Technologies: An Perspective from Iberoamerican Countries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609376/
https://www.ncbi.nlm.nih.gov/pubmed/33145733
http://dx.doi.org/10.1007/s11356-020-11420-9
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