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dc.contributor.author
Ballatore, María Belén  
dc.contributor.author
Spesia, Mariana Belen  
dc.contributor.author
Milanesio, María Elisa  
dc.contributor.author
Durantini, Edgardo Néstor  
dc.date.available
2018-01-26T19:10:09Z  
dc.date.issued
2014-07  
dc.identifier.citation
Ballatore, María Belén; Spesia, Mariana Belen; Milanesio, María Elisa; Durantini, Edgardo Néstor; Synthesis, spectroscopic properties and photodynamic activity of porphyrin–fullerene C60 dyads with application in the photodynamic inactivation of Staphylococcus aureus; Elsevier Masson; European Journal of Medical Chemistry; 83; 7-2014; 685-694  
dc.identifier.issn
0223-5234  
dc.identifier.uri
http://hdl.handle.net/11336/34751  
dc.description.abstract
A covalently linked porphyrin–fullerene C60 dyad 5 was synthesized by 1,3-dipolar cycloaddition using 5-(4-formylphenyl)-10,15,20-tris[3-(N-ethylcarbazoyl)]porphyrin, N-methylglycine and fullerene C60. Methylation of 5 was used to obtain a cationic dyad 6. Spectroscopic properties were compared in toluene, N,N-dimethylformamide (DMF) and toluene/sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/water reverse micelles. Absorption spectra of the dyads were essentially a superposition of the spectra of the porphyrin and fullerene reference compounds, indicating a very weak interaction between the chromophores in the ground state. The fluorescence emission of the porphyrin moiety in the dyads was strongly quenched by the attached fullerene C60 unit. The singlet molecular oxygen, O2(1Δg), productions (ΦΔ) were strongly dependent on the solvent polarity. Similar ΦΔ values were obtained for 5,10,15,20-tetrakis[3-(N-ethylcarbazoyl)]porphyrin (TCP) in both solvents. Also, dyad 5 showed a high O2(1Δg) generation in toluene. However, O2(1Δg) production mediated by 5 considerably diminished in the more polar solvent DMF. Also, a high photodynamic activity involving O2(1Δg) was found for both dyads in a simple biomimetic system formed by AOT reverse micelles. The photoinactivation ability of these dyads was investigated in Staphylococcus aureus cell suspensions. Photosensitized inactivation of S. aureus by dyad 6 exhibits a 4.5 log decrease of cell survival (99.997% cell inactivation), when the cultures are treated with 5 μM photosensitizer and irradiated with visible light (350–800 nm) for 30 min. Under these conditions, a lower photocytotoxic effect was found for 5 (3.2 log decrease). Furthermore, photoinactivation induced by 6 was higher than those obtained with the separate moieties of the dyad. Therefore, molecular structures formed by porphyrin–fullerene C60 dyads represent interesting photosensitizers to inactivate S. aureus.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Masson  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
Dyad  
dc.subject
Photodynamic Properties  
dc.subject.classification
Otras Ciencias Químicas  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Synthesis, spectroscopic properties and photodynamic activity of porphyrin–fullerene C60 dyads with application in the photodynamic inactivation of Staphylococcus aureus  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-01-25T20:46:14Z  
dc.journal.volume
83  
dc.journal.pagination
685-694  
dc.journal.pais
Francia  
dc.journal.ciudad
Paris  
dc.description.fil
Fil: Ballatore, María Belén. 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: Spesia, Mariana Belen. 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: Milanesio, María Elisa. 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: Durantini, Edgardo Néstor. 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.journal.title
European Journal of Medical Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ejmech.2014.06.077  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0223523414006060