Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans
Main Author: | |
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Publication Date: | 2018 |
Other Authors: | , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1016/j.jphotochem.2017.12.020 http://hdl.handle.net/11449/179435 |
Summary: | We report the synthesis, optical, electrochemical and electronic properties of a new perylene derivative and its Ru(II) complex, namely N,-(5-amino-1,10-phenantroline)perylene-3,4,9,10-tetracarboximonoimide (pPDI) and Bis(1,10-phenanthroline)(N-(5-amin-1,10-phenantroline)perylene-3,4,9,10-tetracarboxi monoimide)ruthenium(II) hexafluorophosphate, [Ru(phen)2(pPDI)]2+ ([PF6]−)2. The molecular structures of the compounds were elucidated by FTIR, mass spectrometry, elemental analysis (CHN) and DFT calculations. Their optical and electrochemical properties were investigated by absorption and fluorescence spectroscopy and cyclic voltammetry. The spectroscopic and electrochemical studies for both the pPDI and the perylene monoimide metal complex show that Ru2+ coordination does not affect the optical and electrochemical properties of the free perylene bisimide ligand. The Ru complex exhibits emission lifetimes of 5.06 ns (48.1%) and 156 ns (51.9%), resulting from emission of the pPDI ligand and 3MLCT, respectively. The pPDI triplet excited state in the title chromophore is able to sensitize the production of singlet oxygen (1O2). Using a time-resolved laser system, we measured the quantum yield for the production of singlet oxygen (ΦΔ) to be 0.26 for cis-[Ru(phen)2(pPDI)]2+. Candida albicans is recognized as the most common fungal pathogens, causing superficial infections of the skin and mucous membranes. Resistance of C. albicans strains against classical antifungal agents such as fluconazole has increased considerably, which drives the search for new therapeutic alternatives. In the present study, we report that our new Ru-perylene complex can indeed be used to kill the bacterium C. albicans. The fungicidal activity of cis-[Ru(phen)2(pPDI)]2+ against C. albicans was evaluated in the presence of C. albicans cultures in the dark and in the presence of light. After exposure to 12.5 μM of cis-[Ru(phen)2(pPDI)]2 in the presence of light for 180 s, C. albicans showed a decrease of 50% in its concentration compared to the same experimental conditions in the dark. |
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Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicansCandida albicansPhotodynamic therapy (PDT)PhotoluminescenceRuthenium polypyridine complexSinglet oxygenWe report the synthesis, optical, electrochemical and electronic properties of a new perylene derivative and its Ru(II) complex, namely N,-(5-amino-1,10-phenantroline)perylene-3,4,9,10-tetracarboximonoimide (pPDI) and Bis(1,10-phenanthroline)(N-(5-amin-1,10-phenantroline)perylene-3,4,9,10-tetracarboxi monoimide)ruthenium(II) hexafluorophosphate, [Ru(phen)2(pPDI)]2+ ([PF6]−)2. The molecular structures of the compounds were elucidated by FTIR, mass spectrometry, elemental analysis (CHN) and DFT calculations. Their optical and electrochemical properties were investigated by absorption and fluorescence spectroscopy and cyclic voltammetry. The spectroscopic and electrochemical studies for both the pPDI and the perylene monoimide metal complex show that Ru2+ coordination does not affect the optical and electrochemical properties of the free perylene bisimide ligand. The Ru complex exhibits emission lifetimes of 5.06 ns (48.1%) and 156 ns (51.9%), resulting from emission of the pPDI ligand and 3MLCT, respectively. The pPDI triplet excited state in the title chromophore is able to sensitize the production of singlet oxygen (1O2). Using a time-resolved laser system, we measured the quantum yield for the production of singlet oxygen (ΦΔ) to be 0.26 for cis-[Ru(phen)2(pPDI)]2+. Candida albicans is recognized as the most common fungal pathogens, causing superficial infections of the skin and mucous membranes. Resistance of C. albicans strains against classical antifungal agents such as fluconazole has increased considerably, which drives the search for new therapeutic alternatives. In the present study, we report that our new Ru-perylene complex can indeed be used to kill the bacterium C. albicans. The fungicidal activity of cis-[Ru(phen)2(pPDI)]2+ against C. albicans was evaluated in the presence of C. albicans cultures in the dark and in the presence of light. After exposure to 12.5 μM of cis-[Ru(phen)2(pPDI)]2 in the presence of light for 180 s, C. albicans showed a decrease of 50% in its concentration compared to the same experimental conditions in the dark.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Institute of Exact Sciences and Technology Federal University of AmazonasDepartment of Chemistry Universidade Federal de São Carlos, CP 676Department of Biosciences and Oral Diagnosis Universidade Estadual Paulista/UNESP, Av. Engenheiro Francisco José Longo, 777Department of Chemistry and Biochemistry California State UniversityDepartment of Biosciences and Oral Diagnosis Universidade Estadual Paulista/UNESP, Av. Engenheiro Francisco José Longo, 777Federal University of AmazonasUniversidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)California State UniversityMaia, Paulo José Sousade Aguiar, Inarados Santos Velloso, Marisol [UNESP]Zhang, Dongdos Santos, Edjane Rochade Oliveira, Jonatas Rafael [UNESP]Junqueira, Juliana Campos [UNESP]Selke, MatthiasCarlos, Rose Maria2018-12-11T17:35:10Z2018-12-11T17:35:10Z2018-02-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article536-545application/pdfhttp://dx.doi.org/10.1016/j.jphotochem.2017.12.020Journal of Photochemistry and Photobiology A: Chemistry, v. 353, p. 536-545.1010-6030http://hdl.handle.net/11449/17943510.1016/j.jphotochem.2017.12.0202-s2.0-850380070572-s2.0-85038007057.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Photochemistry and Photobiology A: Chemistry0,689info:eu-repo/semantics/openAccess2024-11-07T13:19:53Zoai:repositorio.unesp.br:11449/179435Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-11-07T13:19:53Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
title |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
spellingShingle |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans Maia, Paulo José Sousa Candida albicans Photodynamic therapy (PDT) Photoluminescence Ruthenium polypyridine complex Singlet oxygen |
title_short |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
title_full |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
title_fullStr |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
title_full_unstemmed |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
title_sort |
Singlet oxygen production by a polypyridine ruthenium (II) complex with a perylene monoimide derivative: A strategy for photodynamic inactivation of Candida albicans |
author |
Maia, Paulo José Sousa |
author_facet |
Maia, Paulo José Sousa de Aguiar, Inara dos Santos Velloso, Marisol [UNESP] Zhang, Dong dos Santos, Edjane Rocha de Oliveira, Jonatas Rafael [UNESP] Junqueira, Juliana Campos [UNESP] Selke, Matthias Carlos, Rose Maria |
author_role |
author |
author2 |
de Aguiar, Inara dos Santos Velloso, Marisol [UNESP] Zhang, Dong dos Santos, Edjane Rocha de Oliveira, Jonatas Rafael [UNESP] Junqueira, Juliana Campos [UNESP] Selke, Matthias Carlos, Rose Maria |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Federal University of Amazonas Universidade Federal de São Carlos (UFSCar) Universidade Estadual Paulista (Unesp) California State University |
dc.contributor.author.fl_str_mv |
Maia, Paulo José Sousa de Aguiar, Inara dos Santos Velloso, Marisol [UNESP] Zhang, Dong dos Santos, Edjane Rocha de Oliveira, Jonatas Rafael [UNESP] Junqueira, Juliana Campos [UNESP] Selke, Matthias Carlos, Rose Maria |
dc.subject.por.fl_str_mv |
Candida albicans Photodynamic therapy (PDT) Photoluminescence Ruthenium polypyridine complex Singlet oxygen |
topic |
Candida albicans Photodynamic therapy (PDT) Photoluminescence Ruthenium polypyridine complex Singlet oxygen |
description |
We report the synthesis, optical, electrochemical and electronic properties of a new perylene derivative and its Ru(II) complex, namely N,-(5-amino-1,10-phenantroline)perylene-3,4,9,10-tetracarboximonoimide (pPDI) and Bis(1,10-phenanthroline)(N-(5-amin-1,10-phenantroline)perylene-3,4,9,10-tetracarboxi monoimide)ruthenium(II) hexafluorophosphate, [Ru(phen)2(pPDI)]2+ ([PF6]−)2. The molecular structures of the compounds were elucidated by FTIR, mass spectrometry, elemental analysis (CHN) and DFT calculations. Their optical and electrochemical properties were investigated by absorption and fluorescence spectroscopy and cyclic voltammetry. The spectroscopic and electrochemical studies for both the pPDI and the perylene monoimide metal complex show that Ru2+ coordination does not affect the optical and electrochemical properties of the free perylene bisimide ligand. The Ru complex exhibits emission lifetimes of 5.06 ns (48.1%) and 156 ns (51.9%), resulting from emission of the pPDI ligand and 3MLCT, respectively. The pPDI triplet excited state in the title chromophore is able to sensitize the production of singlet oxygen (1O2). Using a time-resolved laser system, we measured the quantum yield for the production of singlet oxygen (ΦΔ) to be 0.26 for cis-[Ru(phen)2(pPDI)]2+. Candida albicans is recognized as the most common fungal pathogens, causing superficial infections of the skin and mucous membranes. Resistance of C. albicans strains against classical antifungal agents such as fluconazole has increased considerably, which drives the search for new therapeutic alternatives. In the present study, we report that our new Ru-perylene complex can indeed be used to kill the bacterium C. albicans. The fungicidal activity of cis-[Ru(phen)2(pPDI)]2+ against C. albicans was evaluated in the presence of C. albicans cultures in the dark and in the presence of light. After exposure to 12.5 μM of cis-[Ru(phen)2(pPDI)]2 in the presence of light for 180 s, C. albicans showed a decrease of 50% in its concentration compared to the same experimental conditions in the dark. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:35:10Z 2018-12-11T17:35:10Z 2018-02-15 |
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.jphotochem.2017.12.020 Journal of Photochemistry and Photobiology A: Chemistry, v. 353, p. 536-545. 1010-6030 http://hdl.handle.net/11449/179435 10.1016/j.jphotochem.2017.12.020 2-s2.0-85038007057 2-s2.0-85038007057.pdf |
url |
http://dx.doi.org/10.1016/j.jphotochem.2017.12.020 http://hdl.handle.net/11449/179435 |
identifier_str_mv |
Journal of Photochemistry and Photobiology A: Chemistry, v. 353, p. 536-545. 1010-6030 10.1016/j.jphotochem.2017.12.020 2-s2.0-85038007057 2-s2.0-85038007057.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Photochemistry and Photobiology A: Chemistry 0,689 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
536-545 application/pdf |
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 |
repositoriounesp@unesp.br |
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1834484776178810880 |