Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems

Bibliographic Details
Main Author: Pavan, Nathália Mariana [UNESP]
Publication Date: 2022
Other Authors: Martins, Lucas Michelão [UNESP], Augusto, Laís Cristina [UNESP], da Silva-Filho, Luiz Carlos [UNESP], Ximenes, Valdecir Farias [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.molliq.2022.120137
http://hdl.handle.net/11449/242202
Summary: Hypochlorous acid (HClO) is an endogenous reactive oxygen species generated by the oxidation of chloride catalyzed by myeloperoxidase (MPO). This enzyme is abundant in polymorphonuclear cells and involved in the human innate immune function. This work presents the development of a fluorescent azapentalene (C1) able to be incorporated in micelles and susceptive to HClO due to its sulfide moiety. C1 is non-fluorescent in the aqueous medium but fluoresces when incorporated in micelles produced by surfactants such as sodium dodecyl sulfate (SDS), Triton X-100, and cetyltrimethylammonium chloride (CTAC). The addition of HClO promoted instantaneous fluorescence decay of C1 incorporated in SDS but not in Triton X-100 or CTAC, showing the higher accessibility of HClO to the SDS micelle core. The reactivity of C1 was also studied in the presence of amine compounds taurine, 4-aminobutanoic acid (GABA), and its ethyl ester (GABA-EE), leading to the formation of the respective chloramines. The reactivity increased with the GABA-EE, evidencing the higher accessibility to the micellar core due to the hydrophobic character of the ester derivative. The potentiality of the system to monitor the enzymatic production of HClO was demonstrated by using MPO and hydrogen peroxide (H2O2). Scavengers of HClO were applied to validate the method. In conclusion, applying C1 opens new possibilities for studying the biochemical properties of HClO and chloramines in micelles.
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spelling Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systemsChloraminesFluorescent probesGABAHypochlorous acidMicellesMyeloperoxidaseHypochlorous acid (HClO) is an endogenous reactive oxygen species generated by the oxidation of chloride catalyzed by myeloperoxidase (MPO). This enzyme is abundant in polymorphonuclear cells and involved in the human innate immune function. This work presents the development of a fluorescent azapentalene (C1) able to be incorporated in micelles and susceptive to HClO due to its sulfide moiety. C1 is non-fluorescent in the aqueous medium but fluoresces when incorporated in micelles produced by surfactants such as sodium dodecyl sulfate (SDS), Triton X-100, and cetyltrimethylammonium chloride (CTAC). The addition of HClO promoted instantaneous fluorescence decay of C1 incorporated in SDS but not in Triton X-100 or CTAC, showing the higher accessibility of HClO to the SDS micelle core. The reactivity of C1 was also studied in the presence of amine compounds taurine, 4-aminobutanoic acid (GABA), and its ethyl ester (GABA-EE), leading to the formation of the respective chloramines. The reactivity increased with the GABA-EE, evidencing the higher accessibility to the micellar core due to the hydrophobic character of the ester derivative. The potentiality of the system to monitor the enzymatic production of HClO was demonstrated by using MPO and hydrogen peroxide (H2O2). Scavengers of HClO were applied to validate the method. In conclusion, applying C1 opens new possibilities for studying the biochemical properties of HClO and chloramines in micelles.Department of Chemistry Faculty of Sciences UNESP - São Paulo State University, São PauloDepartment of Chemistry Faculty of Sciences UNESP - São Paulo State University, São PauloUniversidade Estadual Paulista (UNESP)Pavan, Nathália Mariana [UNESP]Martins, Lucas Michelão [UNESP]Augusto, Laís Cristina [UNESP]da Silva-Filho, Luiz Carlos [UNESP]Ximenes, Valdecir Farias [UNESP]2023-03-02T11:50:57Z2023-03-02T11:50:57Z2022-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.molliq.2022.120137Journal of Molecular Liquids, v. 365.0167-7322http://hdl.handle.net/11449/24220210.1016/j.molliq.2022.1201372-s2.0-85136694781Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Molecular Liquidsinfo:eu-repo/semantics/openAccess2023-03-02T11:50:57Zoai:repositorio.unesp.br:11449/242202Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-03-02T11:50:57Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
title Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
spellingShingle Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
Pavan, Nathália Mariana [UNESP]
Chloramines
Fluorescent probes
GABA
Hypochlorous acid
Micelles
Myeloperoxidase
title_short Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
title_full Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
title_fullStr Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
title_full_unstemmed Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
title_sort Development of fluorescent azapentalenes to study the reactivity of hypochlorous acid and chloramines in micellar systems
author Pavan, Nathália Mariana [UNESP]
author_facet Pavan, Nathália Mariana [UNESP]
Martins, Lucas Michelão [UNESP]
Augusto, Laís Cristina [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
Ximenes, Valdecir Farias [UNESP]
author_role author
author2 Martins, Lucas Michelão [UNESP]
Augusto, Laís Cristina [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
Ximenes, Valdecir Farias [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Pavan, Nathália Mariana [UNESP]
Martins, Lucas Michelão [UNESP]
Augusto, Laís Cristina [UNESP]
da Silva-Filho, Luiz Carlos [UNESP]
Ximenes, Valdecir Farias [UNESP]
dc.subject.por.fl_str_mv Chloramines
Fluorescent probes
GABA
Hypochlorous acid
Micelles
Myeloperoxidase
topic Chloramines
Fluorescent probes
GABA
Hypochlorous acid
Micelles
Myeloperoxidase
description Hypochlorous acid (HClO) is an endogenous reactive oxygen species generated by the oxidation of chloride catalyzed by myeloperoxidase (MPO). This enzyme is abundant in polymorphonuclear cells and involved in the human innate immune function. This work presents the development of a fluorescent azapentalene (C1) able to be incorporated in micelles and susceptive to HClO due to its sulfide moiety. C1 is non-fluorescent in the aqueous medium but fluoresces when incorporated in micelles produced by surfactants such as sodium dodecyl sulfate (SDS), Triton X-100, and cetyltrimethylammonium chloride (CTAC). The addition of HClO promoted instantaneous fluorescence decay of C1 incorporated in SDS but not in Triton X-100 or CTAC, showing the higher accessibility of HClO to the SDS micelle core. The reactivity of C1 was also studied in the presence of amine compounds taurine, 4-aminobutanoic acid (GABA), and its ethyl ester (GABA-EE), leading to the formation of the respective chloramines. The reactivity increased with the GABA-EE, evidencing the higher accessibility to the micellar core due to the hydrophobic character of the ester derivative. The potentiality of the system to monitor the enzymatic production of HClO was demonstrated by using MPO and hydrogen peroxide (H2O2). Scavengers of HClO were applied to validate the method. In conclusion, applying C1 opens new possibilities for studying the biochemical properties of HClO and chloramines in micelles.
publishDate 2022
dc.date.none.fl_str_mv 2022-11-01
2023-03-02T11:50:57Z
2023-03-02T11:50:57Z
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.molliq.2022.120137
Journal of Molecular Liquids, v. 365.
0167-7322
http://hdl.handle.net/11449/242202
10.1016/j.molliq.2022.120137
2-s2.0-85136694781
url http://dx.doi.org/10.1016/j.molliq.2022.120137
http://hdl.handle.net/11449/242202
identifier_str_mv Journal of Molecular Liquids, v. 365.
0167-7322
10.1016/j.molliq.2022.120137
2-s2.0-85136694781
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Molecular Liquids
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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