Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.jpba.2020.113349 http://hdl.handle.net/11449/198818 |
Resumo: | Ethofumesate (ETO) is a chiral herbicide that is marketed as a racemic mixture in the European Union and the United States. The growing consumption of pesticides in the world, along with their presence in water and food, has increased human exposure to these chemicals. Another issue concerning these compounds is that each enantiomer of a chiral pesticide may interact with biomolecules differently. For this reason, this study aimed to investigate the in vitro metabolism of ethofumesate (the racemic mixture as well as the isolated enantiomers) by human liver microsomes (HLM) and to explore the in vitro-in vivo correlation. Before the kinetics was determined, the method was fully validated by evaluating its selectivity, linearity, precision, accuracy, carryover, and stability. All the evaluated parameters agreed with the European Medicines Agency guideline. The enzyme kinetic parameters and the in vitro-in vivo correlation demonstrated that there was no enantioselective difference for the metabolism and bioavailable fraction of each enantiomer. The enzyme kinetics was biphasic; the KM1 values were 15, 5.8, and 5.6 for rac-ETO, (+)-ETO, and (–)-ETO, respectively. The total in vitro intrinsic clearance was 0.10 mg mL min−1 mg−1 for rac-ETO and its enantiomers. The enantiomer (–)-ETO was only metabolized by CYP2C19, while (+)-ETO was metabolized by both CYP2C19 and CYP3A4. CYP2C19 polymorphism and/or inhibition may represent a risk for humans exposed to this pesticide. |
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Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human modelenantioselective in vitro metabolismethofumesateGC-MSHerbicidehuman liver microsomesin vitro-in vivo correlationEthofumesate (ETO) is a chiral herbicide that is marketed as a racemic mixture in the European Union and the United States. The growing consumption of pesticides in the world, along with their presence in water and food, has increased human exposure to these chemicals. Another issue concerning these compounds is that each enantiomer of a chiral pesticide may interact with biomolecules differently. For this reason, this study aimed to investigate the in vitro metabolism of ethofumesate (the racemic mixture as well as the isolated enantiomers) by human liver microsomes (HLM) and to explore the in vitro-in vivo correlation. Before the kinetics was determined, the method was fully validated by evaluating its selectivity, linearity, precision, accuracy, carryover, and stability. All the evaluated parameters agreed with the European Medicines Agency guideline. The enzyme kinetic parameters and the in vitro-in vivo correlation demonstrated that there was no enantioselective difference for the metabolism and bioavailable fraction of each enantiomer. The enzyme kinetics was biphasic; the KM1 values were 15, 5.8, and 5.6 for rac-ETO, (+)-ETO, and (–)-ETO, respectively. The total in vitro intrinsic clearance was 0.10 mg mL min−1 mg−1 for rac-ETO and its enantiomers. The enantiomer (–)-ETO was only metabolized by CYP2C19, while (+)-ETO was metabolized by both CYP2C19 and CYP3A4. CYP2C19 polymorphism and/or inhibition may represent a risk for humans exposed to this pesticide.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Departamento de Química Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São PauloNational Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT–DATREM) Unesp Institute of Chemistry, P.O. Box 355National Institute for Alternative Technologies of Detection Toxicological Evaluation and Removal of Micropollutants and Radioactives (INCT–DATREM) Unesp Institute of Chemistry, P.O. Box 355FAPESP: 2014/50945-4FAPESP: 2018/07534-4CNPq: 465571/2014-0Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Perovani, Icaro SalgadoCarrão, Daniel Blasckede Albuquerque, Nayara Cristina Perezde Oliveira, Anderson Rodrigo Moraes [UNESP]2020-12-12T01:22:47Z2020-12-12T01:22:47Z2020-08-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.jpba.2020.113349Journal of Pharmaceutical and Biomedical Analysis, v. 187.1873-264X0731-7085http://hdl.handle.net/11449/19881810.1016/j.jpba.2020.1133492-s2.0-85084366715Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Pharmaceutical and Biomedical Analysisinfo:eu-repo/semantics/openAccess2021-10-22T20:36:13Zoai:repositorio.unesp.br:11449/198818Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:44:25.942048Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
title |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
spellingShingle |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model Perovani, Icaro Salgado enantioselective in vitro metabolism ethofumesate GC-MS Herbicide human liver microsomes in vitro-in vivo correlation |
title_short |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
title_full |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
title_fullStr |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
title_full_unstemmed |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
title_sort |
Enantioselective in vitro metabolism and in vitro-in vivo correlation of the herbicide ethofumesate in a human model |
author |
Perovani, Icaro Salgado |
author_facet |
Perovani, Icaro Salgado Carrão, Daniel Blascke de Albuquerque, Nayara Cristina Perez de Oliveira, Anderson Rodrigo Moraes [UNESP] |
author_role |
author |
author2 |
Carrão, Daniel Blascke de Albuquerque, Nayara Cristina Perez de Oliveira, Anderson Rodrigo Moraes [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Perovani, Icaro Salgado Carrão, Daniel Blascke de Albuquerque, Nayara Cristina Perez de Oliveira, Anderson Rodrigo Moraes [UNESP] |
dc.subject.por.fl_str_mv |
enantioselective in vitro metabolism ethofumesate GC-MS Herbicide human liver microsomes in vitro-in vivo correlation |
topic |
enantioselective in vitro metabolism ethofumesate GC-MS Herbicide human liver microsomes in vitro-in vivo correlation |
description |
Ethofumesate (ETO) is a chiral herbicide that is marketed as a racemic mixture in the European Union and the United States. The growing consumption of pesticides in the world, along with their presence in water and food, has increased human exposure to these chemicals. Another issue concerning these compounds is that each enantiomer of a chiral pesticide may interact with biomolecules differently. For this reason, this study aimed to investigate the in vitro metabolism of ethofumesate (the racemic mixture as well as the isolated enantiomers) by human liver microsomes (HLM) and to explore the in vitro-in vivo correlation. Before the kinetics was determined, the method was fully validated by evaluating its selectivity, linearity, precision, accuracy, carryover, and stability. All the evaluated parameters agreed with the European Medicines Agency guideline. The enzyme kinetic parameters and the in vitro-in vivo correlation demonstrated that there was no enantioselective difference for the metabolism and bioavailable fraction of each enantiomer. The enzyme kinetics was biphasic; the KM1 values were 15, 5.8, and 5.6 for rac-ETO, (+)-ETO, and (–)-ETO, respectively. The total in vitro intrinsic clearance was 0.10 mg mL min−1 mg−1 for rac-ETO and its enantiomers. The enantiomer (–)-ETO was only metabolized by CYP2C19, while (+)-ETO was metabolized by both CYP2C19 and CYP3A4. CYP2C19 polymorphism and/or inhibition may represent a risk for humans exposed to this pesticide. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-12T01:22:47Z 2020-12-12T01:22:47Z 2020-08-05 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.jpba.2020.113349 Journal of Pharmaceutical and Biomedical Analysis, v. 187. 1873-264X 0731-7085 http://hdl.handle.net/11449/198818 10.1016/j.jpba.2020.113349 2-s2.0-85084366715 |
url |
http://dx.doi.org/10.1016/j.jpba.2020.113349 http://hdl.handle.net/11449/198818 |
identifier_str_mv |
Journal of Pharmaceutical and Biomedical Analysis, v. 187. 1873-264X 0731-7085 10.1016/j.jpba.2020.113349 2-s2.0-85084366715 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Pharmaceutical and Biomedical Analysis |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808128555982258176 |