Reactivity of paraquat with sodium salicylate: formation of stable complexes

Detalhes bibliográficos
Autor(a) principal: Dinis-Oliveira, Ricardo Jorge
Data de Publicação: 2008
Outros Autores: Pinho, Paula Guedes de, Ferreira, Antonio César Silva, Silva, Artur M. S., Afonso, Carlos, Bastos, Maria de Lourdes, Remião, Fernando, Duarte, José Alberto, Carvalho, Félix
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.14/2759
Resumo: Sodium salicylate (NaSAL) has been shown to be a promising antidote for the treatment of paraquat (PQ) poisonings. The modulation of the pro-oxidant and pro-inflammatory pathways, as well as the antithrombogenic properties of NaSAL are probably essential features for the healing effects provided by this drug. Nevertheless, a possible direct chemical reactivity between PQ and NaSAL is also a putative pathway to be considered, this hypothesis being the ground of the present study. In accordance, it is shown, for the first time that PQ and NaSAL react immediately in aqueous medium and within 2–3 min in the solid state. Photographs and scanning electron photomicrographs indicated that a new chemical entity is formed when both compounds are mixed. This assumption was corroborated by the evaluation of the melting point, and through several analytical techniques, namely ultraviolet/visible spectroscopy, nuclear magnetic resonance spectroscopy, gas chromatography/mass spectrometry/mass spectrometry (GC/MS/MS), liquid chromatography/electrospray ionization/mass spectrometry/mass spectrometry (LC/ESI/MS/MS) and infrared spectroscopy, which revealed that stable charge-transfer complexes are formed when PQ is mixed with NaSAL. LC/ESI/MS/MS allowed obtaining the stoichiometry of the charge-transfer complexes. In order to increase resolution, single value decomposition, acting as a filter, showed that the chargetransfer complexes withm/z 483, 643 and 803 correspond to the pseudo-molecular ions, respectively 1:2, 1:3 and 1:4 (PQ:NaSAL). In conclusion, these results provided a new and important mechanism of action of NaSAL against the toxicity mediated by PQ.
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spelling Reactivity of paraquat with sodium salicylate: formation of stable complexesParaquatSodium salicylateCharge-transfer complexesSodium salicylate (NaSAL) has been shown to be a promising antidote for the treatment of paraquat (PQ) poisonings. The modulation of the pro-oxidant and pro-inflammatory pathways, as well as the antithrombogenic properties of NaSAL are probably essential features for the healing effects provided by this drug. Nevertheless, a possible direct chemical reactivity between PQ and NaSAL is also a putative pathway to be considered, this hypothesis being the ground of the present study. In accordance, it is shown, for the first time that PQ and NaSAL react immediately in aqueous medium and within 2–3 min in the solid state. Photographs and scanning electron photomicrographs indicated that a new chemical entity is formed when both compounds are mixed. This assumption was corroborated by the evaluation of the melting point, and through several analytical techniques, namely ultraviolet/visible spectroscopy, nuclear magnetic resonance spectroscopy, gas chromatography/mass spectrometry/mass spectrometry (GC/MS/MS), liquid chromatography/electrospray ionization/mass spectrometry/mass spectrometry (LC/ESI/MS/MS) and infrared spectroscopy, which revealed that stable charge-transfer complexes are formed when PQ is mixed with NaSAL. LC/ESI/MS/MS allowed obtaining the stoichiometry of the charge-transfer complexes. In order to increase resolution, single value decomposition, acting as a filter, showed that the chargetransfer complexes withm/z 483, 643 and 803 correspond to the pseudo-molecular ions, respectively 1:2, 1:3 and 1:4 (PQ:NaSAL). In conclusion, these results provided a new and important mechanism of action of NaSAL against the toxicity mediated by PQ.ElsevierVeritati - Repositório Institucional da Universidade Católica PortuguesaDinis-Oliveira, Ricardo JorgePinho, Paula Guedes deFerreira, Antonio César SilvaSilva, Artur M. S.Afonso, CarlosBastos, Maria de LourdesRemião, FernandoDuarte, José AlbertoCarvalho, Félix2010-10-11T09:50:10Z20082008-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/2759eng"Toxicology". ISSN 0300-483X. 249: 2-3 (2008) 130–13910.1016/j.tox.2008.04.014info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-12T17:09:20Zoai:repositorio.ucp.pt:10400.14/2759Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:04:59.789582Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Reactivity of paraquat with sodium salicylate: formation of stable complexes
title Reactivity of paraquat with sodium salicylate: formation of stable complexes
spellingShingle Reactivity of paraquat with sodium salicylate: formation of stable complexes
Dinis-Oliveira, Ricardo Jorge
Paraquat
Sodium salicylate
Charge-transfer complexes
title_short Reactivity of paraquat with sodium salicylate: formation of stable complexes
title_full Reactivity of paraquat with sodium salicylate: formation of stable complexes
title_fullStr Reactivity of paraquat with sodium salicylate: formation of stable complexes
title_full_unstemmed Reactivity of paraquat with sodium salicylate: formation of stable complexes
title_sort Reactivity of paraquat with sodium salicylate: formation of stable complexes
author Dinis-Oliveira, Ricardo Jorge
author_facet Dinis-Oliveira, Ricardo Jorge
Pinho, Paula Guedes de
Ferreira, Antonio César Silva
Silva, Artur M. S.
Afonso, Carlos
Bastos, Maria de Lourdes
Remião, Fernando
Duarte, José Alberto
Carvalho, Félix
author_role author
author2 Pinho, Paula Guedes de
Ferreira, Antonio César Silva
Silva, Artur M. S.
Afonso, Carlos
Bastos, Maria de Lourdes
Remião, Fernando
Duarte, José Alberto
Carvalho, Félix
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Veritati - Repositório Institucional da Universidade Católica Portuguesa
dc.contributor.author.fl_str_mv Dinis-Oliveira, Ricardo Jorge
Pinho, Paula Guedes de
Ferreira, Antonio César Silva
Silva, Artur M. S.
Afonso, Carlos
Bastos, Maria de Lourdes
Remião, Fernando
Duarte, José Alberto
Carvalho, Félix
dc.subject.por.fl_str_mv Paraquat
Sodium salicylate
Charge-transfer complexes
topic Paraquat
Sodium salicylate
Charge-transfer complexes
description Sodium salicylate (NaSAL) has been shown to be a promising antidote for the treatment of paraquat (PQ) poisonings. The modulation of the pro-oxidant and pro-inflammatory pathways, as well as the antithrombogenic properties of NaSAL are probably essential features for the healing effects provided by this drug. Nevertheless, a possible direct chemical reactivity between PQ and NaSAL is also a putative pathway to be considered, this hypothesis being the ground of the present study. In accordance, it is shown, for the first time that PQ and NaSAL react immediately in aqueous medium and within 2–3 min in the solid state. Photographs and scanning electron photomicrographs indicated that a new chemical entity is formed when both compounds are mixed. This assumption was corroborated by the evaluation of the melting point, and through several analytical techniques, namely ultraviolet/visible spectroscopy, nuclear magnetic resonance spectroscopy, gas chromatography/mass spectrometry/mass spectrometry (GC/MS/MS), liquid chromatography/electrospray ionization/mass spectrometry/mass spectrometry (LC/ESI/MS/MS) and infrared spectroscopy, which revealed that stable charge-transfer complexes are formed when PQ is mixed with NaSAL. LC/ESI/MS/MS allowed obtaining the stoichiometry of the charge-transfer complexes. In order to increase resolution, single value decomposition, acting as a filter, showed that the chargetransfer complexes withm/z 483, 643 and 803 correspond to the pseudo-molecular ions, respectively 1:2, 1:3 and 1:4 (PQ:NaSAL). In conclusion, these results provided a new and important mechanism of action of NaSAL against the toxicity mediated by PQ.
publishDate 2008
dc.date.none.fl_str_mv 2008
2008-01-01T00:00:00Z
2010-10-11T09:50:10Z
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://hdl.handle.net/10400.14/2759
url http://hdl.handle.net/10400.14/2759
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv "Toxicology". ISSN 0300-483X. 249: 2-3 (2008) 130–139
10.1016/j.tox.2008.04.014
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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