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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