Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1111/php.13410 http://hdl.handle.net/11449/206026 |
Resumo: | Singlet oxygen (1O2) is the “active principle” in photodynamic therapy. Taurine chloramine (Tau-NHCl) and hydrogen peroxide (H2O2) are well-tolerated and widely used antiseptics. Due to its mild oxidizing features and stability, Tau-NHCl can be directly used to treat skin diseases. We found that a diluted aqueous mixture of Tau-NHCl and H2O2 acts as a slow and long-lasting potential source of 1O2. The reactions were studied by luminol-enhanced chemiluminescence. Evidence of the formation of 1O2 was obtained using deuterium oxide, sodium azide and 9,10-Anthracenediyl-bis(methylene)dimalonic acid, a chemical trap of 1O2. The reaction was optimized, and a mechanism was proposed, including theoretical calculations at B3LYP/6-311++G(3df,2p) level of theory, adding D3Bj empirical dispersion and SMD (Water) solvent effects. Chloramines produced by the reactions between HOCl and L-alanine, 3-amino-1-propanesulfonic acid and gamma-aminobutyric acid were also prepared, and their reactivity and stability were compared with Tau-NHCl. We found that Tau-NHCl is more stable and adequate for the production of 1O2. In conclusion, we propose applying these drugs combination as a potential source of 1O2 with applications for skin diseases treatment. |
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Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical ApplicationSinglet oxygen (1O2) is the “active principle” in photodynamic therapy. Taurine chloramine (Tau-NHCl) and hydrogen peroxide (H2O2) are well-tolerated and widely used antiseptics. Due to its mild oxidizing features and stability, Tau-NHCl can be directly used to treat skin diseases. We found that a diluted aqueous mixture of Tau-NHCl and H2O2 acts as a slow and long-lasting potential source of 1O2. The reactions were studied by luminol-enhanced chemiluminescence. Evidence of the formation of 1O2 was obtained using deuterium oxide, sodium azide and 9,10-Anthracenediyl-bis(methylene)dimalonic acid, a chemical trap of 1O2. The reaction was optimized, and a mechanism was proposed, including theoretical calculations at B3LYP/6-311++G(3df,2p) level of theory, adding D3Bj empirical dispersion and SMD (Water) solvent effects. Chloramines produced by the reactions between HOCl and L-alanine, 3-amino-1-propanesulfonic acid and gamma-aminobutyric acid were also prepared, and their reactivity and stability were compared with Tau-NHCl. We found that Tau-NHCl is more stable and adequate for the production of 1O2. In conclusion, we propose applying these drugs combination as a potential source of 1O2 with applications for skin diseases treatment.Department of Chemistry Faculty of Sciences UNESP - São Paulo State UniversityDepartment of Physical Chemistry Institute of Chemistry Campinas State University (UNICAMP)Department of Chemistry Faculty of Sciences UNESP - São Paulo State UniversityUniversidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Ximenes, Valdecir F. [UNESP]Ximenes, Thomaz P. [UNESP]Morgon, Nelson H.de Souza, Aguinaldo R. [UNESP]2021-06-25T10:25:21Z2021-06-25T10:25:21Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1111/php.13410Photochemistry and Photobiology.1751-10970031-8655http://hdl.handle.net/11449/20602610.1111/php.134102-s2.0-85102290146Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhotochemistry and Photobiologyinfo:eu-repo/semantics/openAccess2021-10-22T20:42:33Zoai:repositorio.unesp.br:11449/206026Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:19:42.604856Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
title |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
spellingShingle |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application Ximenes, Valdecir F. [UNESP] |
title_short |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
title_full |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
title_fullStr |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
title_full_unstemmed |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
title_sort |
Taurine Chloramine and Hydrogen Peroxide as a Potential Source of Singlet Oxygen for Topical Application |
author |
Ximenes, Valdecir F. [UNESP] |
author_facet |
Ximenes, Valdecir F. [UNESP] Ximenes, Thomaz P. [UNESP] Morgon, Nelson H. de Souza, Aguinaldo R. [UNESP] |
author_role |
author |
author2 |
Ximenes, Thomaz P. [UNESP] Morgon, Nelson H. de Souza, Aguinaldo R. [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Estadual de Campinas (UNICAMP) |
dc.contributor.author.fl_str_mv |
Ximenes, Valdecir F. [UNESP] Ximenes, Thomaz P. [UNESP] Morgon, Nelson H. de Souza, Aguinaldo R. [UNESP] |
description |
Singlet oxygen (1O2) is the “active principle” in photodynamic therapy. Taurine chloramine (Tau-NHCl) and hydrogen peroxide (H2O2) are well-tolerated and widely used antiseptics. Due to its mild oxidizing features and stability, Tau-NHCl can be directly used to treat skin diseases. We found that a diluted aqueous mixture of Tau-NHCl and H2O2 acts as a slow and long-lasting potential source of 1O2. The reactions were studied by luminol-enhanced chemiluminescence. Evidence of the formation of 1O2 was obtained using deuterium oxide, sodium azide and 9,10-Anthracenediyl-bis(methylene)dimalonic acid, a chemical trap of 1O2. The reaction was optimized, and a mechanism was proposed, including theoretical calculations at B3LYP/6-311++G(3df,2p) level of theory, adding D3Bj empirical dispersion and SMD (Water) solvent effects. Chloramines produced by the reactions between HOCl and L-alanine, 3-amino-1-propanesulfonic acid and gamma-aminobutyric acid were also prepared, and their reactivity and stability were compared with Tau-NHCl. We found that Tau-NHCl is more stable and adequate for the production of 1O2. In conclusion, we propose applying these drugs combination as a potential source of 1O2 with applications for skin diseases treatment. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-25T10:25:21Z 2021-06-25T10:25:21Z 2021-01-01 |
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/10.1111/php.13410 Photochemistry and Photobiology. 1751-1097 0031-8655 http://hdl.handle.net/11449/206026 10.1111/php.13410 2-s2.0-85102290146 |
url |
http://dx.doi.org/10.1111/php.13410 http://hdl.handle.net/11449/206026 |
identifier_str_mv |
Photochemistry and Photobiology. 1751-1097 0031-8655 10.1111/php.13410 2-s2.0-85102290146 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Photochemistry and Photobiology |
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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1808128791507107840 |