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dc.contributor.author
Vara, Jimena  
dc.contributor.author
Gualdesi, María Soledad  
dc.contributor.author
Bertolotti, Sonia Graciela  
dc.contributor.author
Ortiz, Cristina Susana  
dc.date.available
2020-09-01T19:32:46Z  
dc.date.issued
2019-04  
dc.identifier.citation
Vara, Jimena; Gualdesi, María Soledad; Bertolotti, Sonia Graciela; Ortiz, Cristina Susana; Two phenothiazine dyes as photosensitizers for the production of singlet oxygen. Photophysics, photochemistry and effects of aggregation; Elsevier Science; Journal of Molecular Structure; 1181; 4-2019; 1-7  
dc.identifier.issn
0022-2860  
dc.identifier.uri
http://hdl.handle.net/11336/112936  
dc.description.abstract
The aim of this work was to investigate the aggregation effect of Azure B and monobrominated Azure B on their singlet oxygen generation. The monomeric and dimeric forms of these dyes were evaluated to select the species with better properties as photosensitizers. The results demonstrate that the monomeric forms are better producers of singlet oxygen than their aggregated species. However, the dimeric species of monobrominated Azure B is also a good producer of singlet oxygen. The bromination of this phenothiazine dye significantly increases the singlet oxygen quantum yields of the monomeric and dimeric species, enhancing its properties like photosensitizer and its application in Photodynamic Therapy. In addition, significant differences were observed in the singlet oxygen production of the monomeric forms of both photosensitizers determined by phosphorescence decay of singlet oxygen and photooxidation of 9,10-dimethylanthracene (DMA). The physicochemical interaction between the excited species of the phenothiazine monomers and the molecules of DMA could be responsible for the lower values of singlet oxygen production because the disaggregated forms did not present any activity as physical or chemical attenuators. The dimeric form of phenothiazine dyes did not show this interaction. In conclusion, there is a need for developing vehiculization systems that stabilize the monomers of phenothiazine dyes because they have better properties than their aggregates in terms of singlet oxygen production.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
AZURE B  
dc.subject
MONOBROMINATED AZURE B  
dc.subject
MONOMER- DIMER- SINGLET OXYGEN  
dc.subject.classification
Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Two phenothiazine dyes as photosensitizers for the production of singlet oxygen. Photophysics, photochemistry and effects of aggregation  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-08-21T15:42:10Z  
dc.journal.volume
1181  
dc.journal.pagination
1-7  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Vara, Jimena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina  
dc.description.fil
Fil: Gualdesi, María Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina  
dc.description.fil
Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Ortiz, Cristina Susana. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; Argentina  
dc.journal.title
Journal of Molecular Structure  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0022286018315114  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.molstruc.2018.12.078