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Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro

Currently, the authorisation process for plant protection products (PPPs) relies on the testing of acute and topological toxicity only. Contrastingly, the evaluation of active substances includes a more comprehensive set of toxicity studies. Nevertheless, mixture effects of active ingredients and co...

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Autores principales: Karaca, Mawien, Fischer, Benjamin Christian, Willenbockel, Christian Tobias, Tralau, Tewes, Marx-Stoelting, Philip, Bloch, Denise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448693/
https://www.ncbi.nlm.nih.gov/pubmed/34417632
http://dx.doi.org/10.1007/s00204-021-03140-x
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author Karaca, Mawien
Fischer, Benjamin Christian
Willenbockel, Christian Tobias
Tralau, Tewes
Marx-Stoelting, Philip
Bloch, Denise
author_facet Karaca, Mawien
Fischer, Benjamin Christian
Willenbockel, Christian Tobias
Tralau, Tewes
Marx-Stoelting, Philip
Bloch, Denise
author_sort Karaca, Mawien
collection PubMed
description Currently, the authorisation process for plant protection products (PPPs) relies on the testing of acute and topological toxicity only. Contrastingly, the evaluation of active substances includes a more comprehensive set of toxicity studies. Nevertheless, mixture effects of active ingredients and co-formulants may result in increased toxicity. Therefore, we investigated effects of surface active co-formulants on the toxicity of two PPPs focussing on qualitative and quantitative toxicokinetic effects on absorption and secretion. The respective products are based on the active substances abamectin and fluroxypyr-meptyl and were tested for cytotoxicity in the presence or absence of the corresponding surfactants and co-formulants using Caco-2 cells. In addition, the effect of co-formulants on increased cellular permeation was quantified using LC–MS/MS, while potential kinetic mixture effects were addressed by fluorescence anisotropy measurements and ATPase assays. The results show that surface active co-formulants significantly increase the cytotoxicity of the investigated PPPs, leading to more than additive mixture effects. Moreover, analytical investigations show higher efflux ratios of both active substances and the metabolite fluroxypyr upon combination with certain concentrations of the surfactants. The results further point to a significant and concentration-dependent inhibition of Pgp transporters by most of the surfactants as well as to increased membrane fluidity. Altogether, these findings strongly support the hypothesis that surfactants contribute to increased cytotoxicity of PPPs and do so by increasing the bioavailability of the respective active substances. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-03140-x.
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spelling pubmed-84486932021-10-01 Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro Karaca, Mawien Fischer, Benjamin Christian Willenbockel, Christian Tobias Tralau, Tewes Marx-Stoelting, Philip Bloch, Denise Arch Toxicol Toxicokinetics and Metabolism Currently, the authorisation process for plant protection products (PPPs) relies on the testing of acute and topological toxicity only. Contrastingly, the evaluation of active substances includes a more comprehensive set of toxicity studies. Nevertheless, mixture effects of active ingredients and co-formulants may result in increased toxicity. Therefore, we investigated effects of surface active co-formulants on the toxicity of two PPPs focussing on qualitative and quantitative toxicokinetic effects on absorption and secretion. The respective products are based on the active substances abamectin and fluroxypyr-meptyl and were tested for cytotoxicity in the presence or absence of the corresponding surfactants and co-formulants using Caco-2 cells. In addition, the effect of co-formulants on increased cellular permeation was quantified using LC–MS/MS, while potential kinetic mixture effects were addressed by fluorescence anisotropy measurements and ATPase assays. The results show that surface active co-formulants significantly increase the cytotoxicity of the investigated PPPs, leading to more than additive mixture effects. Moreover, analytical investigations show higher efflux ratios of both active substances and the metabolite fluroxypyr upon combination with certain concentrations of the surfactants. The results further point to a significant and concentration-dependent inhibition of Pgp transporters by most of the surfactants as well as to increased membrane fluidity. Altogether, these findings strongly support the hypothesis that surfactants contribute to increased cytotoxicity of PPPs and do so by increasing the bioavailability of the respective active substances. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-03140-x. Springer Berlin Heidelberg 2021-08-20 2021 /pmc/articles/PMC8448693/ /pubmed/34417632 http://dx.doi.org/10.1007/s00204-021-03140-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Toxicokinetics and Metabolism
Karaca, Mawien
Fischer, Benjamin Christian
Willenbockel, Christian Tobias
Tralau, Tewes
Marx-Stoelting, Philip
Bloch, Denise
Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title_full Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title_fullStr Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title_full_unstemmed Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title_short Effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
title_sort effects of co-formulants on the absorption and secretion of active substances in plant protection products in vitro
topic Toxicokinetics and Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448693/
https://www.ncbi.nlm.nih.gov/pubmed/34417632
http://dx.doi.org/10.1007/s00204-021-03140-x
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