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dc.contributor.author
Urrutia, María Noel

dc.contributor.author
Ortiz, Cristina Susana

dc.date.available
2018-07-13T18:05:39Z
dc.date.issued
2016-11
dc.identifier.citation
Urrutia, María Noel; Ortiz, Cristina Susana; Novel oxazine and oxazone dyes: aggregation behavior and physicochemical properties; Royal Society of Chemistry; New Journal of Chemistry; 40; 12; 11-2016; 10161-10171
dc.identifier.issn
1144-0546
dc.identifier.uri
http://hdl.handle.net/11336/52054
dc.description.abstract
This research evaluated the synthesis and suitability of synthetic and commercial photosensitizers for use as potential photosensitizers in photodynamic therapy and photodynamic antimicrobial chemotherapy. Spectroscopic properties, experimental aggregation behavior in ethanol, N,N-dimethylformamide, water and water:polyethylene glycol 400, computational details, the ability to generate singlet oxygen, logPHPLC and theoretical logP were determined. All the compounds evaluated formed aggregates in different media. Novel brominated tested compounds exhibited higher lipophilicity and generation of singlet oxygen in comparison with the corresponding starting reagent. The studies showed that the tested oxazine and oxazone dyes satisfy the conditions of a potential drug in terms of physicochemical and photochemical properties.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Royal Society of Chemistry

dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Cresyl Violet
dc.subject
Cresyl Red
dc.subject
Synthesis
dc.subject
Aggregation
dc.subject.classification
Otras Ciencias Químicas

dc.subject.classification
Ciencias Químicas

dc.subject.classification
CIENCIAS NATURALES Y EXACTAS

dc.title
Novel oxazine and oxazone dyes: aggregation behavior and physicochemical properties
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-06-25T01:04:08Z
dc.journal.volume
40
dc.journal.number
12
dc.journal.pagination
10161-10171
dc.journal.pais
Reino Unido

dc.description.fil
Fil: Urrutia, María Noel. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; 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. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.journal.title
New Journal of Chemistry

dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C6NJ02053D
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2016/NJ/C6NJ02053D
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