Mostrar el registro sencillo del ítem

dc.contributor.author
Spesia, Mariana Belen  
dc.contributor.author
Milanesio, María Elisa  
dc.contributor.author
Durantini, Edgardo Néstor  
dc.date.available
2024-08-09T10:57:50Z  
dc.date.issued
2008-04  
dc.identifier.citation
Spesia, Mariana Belen; Milanesio, María Elisa; Durantini, Edgardo Néstor; Synthesis, properties and photodynamic inactivation of Escherichia coli by novel cationic fullerene C60 derivatives; Elsevier France-Editions Scientifiques Medicales Elsevier; European Journal of Medical Chemistry; 43; 4; 4-2008; 853-861  
dc.identifier.issn
0223-5234  
dc.identifier.uri
http://hdl.handle.net/11336/242174  
dc.description.abstract
A novel N,N-dimethyl-2-(40-N,N,N-trimethylaminophenyl)fulleropyrrolidinium iodide (DTC602+) has been synthesized by 1,3-dipolar cycloaddition using 4-(N,N-dimethylamino) benzaldehyde, N-methylglycine and fullerene C60. This approach produced an N-methyl-2-(40-N,N-dimethylaminophenyl) fulleropyrrolidine with 38% yield. Exhaustive methylation of this fullerene derivative with methyl iodide yielded 95% of dicationic DTC602+. The spectroscopic and photodynamic properties of the DTC602+were compared with a non-charged N-methyl-2-(40-acetamidophenyl)fulleropyrrolidine (MAC60) and a monocationic N,N-dimethyl-2-(40-acetamidophenyl)fulleropyrrolidinium iodide (DTC602+). The dicationic DTC602+is essentially aggregated in solution of different solvents and it is partially dissolved as monomer in benzene/benzyl-n-hexadecyldimethyl ammonium chloride (BHDC) 0.1 M/water (W0 = 10) reverse micelles. The singlet molecular oxygen, O2 (1Dg), production was evaluated using 1,3-diphenylisobenzofuran. The photodynamic effect was strongly dependent on the medium, diminishes when the sensitizer is aggregated and increases in an appropriately surrounded microenvironment. The photodynamic inactivation produced by these fullerene derivatives was investigated in vitro on a typical Gram-negative bacterium, Escherichia coli. Photosensitized inactivation of E. coli cellular suspensions by DTC602+ exhibits aw3.5 log decrease of cell survival (99.97% of cellular inactivation), when the cultures are treated with 1 mM of sensitizer and irradiated for 30 min. This photosensitized inactivation remains high even after one washing step. Also, the photodynamic activity was confirmed by growth delay of E. coli cultures. The growth was arrested when E. coli was exposed to 2 mM of cationic fullerene and irradiated, whereas a negligible effect was found for the non-charged MAC60. These studies indicate that dicationic DTC602+ is an interesting agent with potential applications in photodynamic inactivation of bacteria.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier France-Editions Scientifiques Medicales Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Fullerene  
dc.subject
Synthesis  
dc.subject
Photodynamic inactivation  
dc.subject.classification
Biología Celular, Microbiología  
dc.subject.classification
Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Synthesis, properties and photodynamic inactivation of Escherichia coli by novel cationic fullerene C60 derivatives  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-08-08T15:43:24Z  
dc.journal.volume
43  
dc.journal.number
4  
dc.journal.pagination
853-861  
dc.journal.pais
Francia  
dc.description.fil
Fil: Spesia, Mariana Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales. Departamento de Química; 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. Centro Científico Tecnológico Conicet - Córdoba; 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. Centro Científico Tecnológico Conicet - Córdoba; Argentina  
dc.journal.title
European Journal of Medical Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0223523407002644  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ejmech.2007.06.014