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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
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Ciencias Biológicas
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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
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