Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative
- Autores
- Spesia, Mariana Belen; Durantini, Edgardo Néstor
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A novel chloro[2,9,16(2,9,17)-trikis-4-(N-methylpyridyloxy)]subphthalocyaninnato boron(III) iodide (SubOPc3+) has been synthesized by boron trichloride-induced cyclotrimerization of 4-(4-pyridyloxy)phthalonitrile in 1-chloronaphthalene. This approach produced a regioisomers mixture of chloro[2,9,16(2,9,17)-trikis-4-(pyridyloxy)]subphthalocyaninnato boron(III) (SubOPc) with 19% yield. Exhaustive methylation of SubOPc with methyl iodide yielded 92% of tricationic SubOPc3+. The spectroscopic and photodynamic properties of the SubOPc3+ were compared with its homologous non-charged SubOPc and with subphthalocyanine (SubPc). The cationic SubOPc3+ is essentially aggregated in solution of different solvents and it is partially dissolved as monomer in aqueous sodium dodecyl sulfate (SDS) 2% w/v. The photodynamic effect was strongly dependent of the medium, increasing in an appropriated surrounding microenvironment. The photodynamic inactivation produced by these subphthalocyanines was for first time investigated in vitro on a typical Gram-negative bacterium, Escherichia coli. Cationic SubOPc3+ is rapidly bound to E. coli cells reaching a value of ~2 nmol/106 cells after 5 min of incubation with 4 mM of sensitizer in dark. Photosensitized inactivation of E. coli cellular suspensions by SubOPc3+ exhibits a ~2.5 log decrease of cell survival (99.7 % of cellular inactivation), when the cultures are irradiated for 30 min. The growth of E. coli cells was completely arrested when the cultures were exposed to 8 mM of cationic subphthalocyanine and irradiated, whereas a negligible effect was found for the non-charged SubOPc. Also, SubOPc3+ remains a high activity to inactivate E. coli cells immobilized on agar surfaces. Therefore, the reported results indicate that tricationic subphthalocyanines are interesting photosensitizers with useful antibacterial activity.
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. Centro Científico Tecnológico Conicet - Córdoba; Argentina
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 - Materia
-
Subphthalocyanine
Photosensitizer
Bacteria
Photodynamic inactivation - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/241094
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Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivativeSpesia, Mariana BelenDurantini, Edgardo NéstorSubphthalocyaninePhotosensitizerBacteriaPhotodynamic inactivationhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A novel chloro[2,9,16(2,9,17)-trikis-4-(N-methylpyridyloxy)]subphthalocyaninnato boron(III) iodide (SubOPc3+) has been synthesized by boron trichloride-induced cyclotrimerization of 4-(4-pyridyloxy)phthalonitrile in 1-chloronaphthalene. This approach produced a regioisomers mixture of chloro[2,9,16(2,9,17)-trikis-4-(pyridyloxy)]subphthalocyaninnato boron(III) (SubOPc) with 19% yield. Exhaustive methylation of SubOPc with methyl iodide yielded 92% of tricationic SubOPc3+. The spectroscopic and photodynamic properties of the SubOPc3+ were compared with its homologous non-charged SubOPc and with subphthalocyanine (SubPc). The cationic SubOPc3+ is essentially aggregated in solution of different solvents and it is partially dissolved as monomer in aqueous sodium dodecyl sulfate (SDS) 2% w/v. The photodynamic effect was strongly dependent of the medium, increasing in an appropriated surrounding microenvironment. The photodynamic inactivation produced by these subphthalocyanines was for first time investigated in vitro on a typical Gram-negative bacterium, Escherichia coli. Cationic SubOPc3+ is rapidly bound to E. coli cells reaching a value of ~2 nmol/106 cells after 5 min of incubation with 4 mM of sensitizer in dark. Photosensitized inactivation of E. coli cellular suspensions by SubOPc3+ exhibits a ~2.5 log decrease of cell survival (99.7 % of cellular inactivation), when the cultures are irradiated for 30 min. The growth of E. coli cells was completely arrested when the cultures were exposed to 8 mM of cationic subphthalocyanine and irradiated, whereas a negligible effect was found for the non-charged SubOPc. Also, SubOPc3+ remains a high activity to inactivate E. coli cells immobilized on agar surfaces. Therefore, the reported results indicate that tricationic subphthalocyanines are interesting photosensitizers with useful antibacterial activity.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. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: 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; ArgentinaElsevier2008-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/241094Spesia, Mariana Belen; Durantini, Edgardo Néstor; Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative; Elsevier; Dyes and Pigments; 77; 1; 6-2008; 229-2370143-7208CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0143720807001179info:eu-repo/semantics/altIdentifier/doi/10.1016/j.dyepig.2007.05.008info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:21:09Zoai:ri.conicet.gov.ar:11336/241094instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:21:10.22CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
title |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
spellingShingle |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative Spesia, Mariana Belen Subphthalocyanine Photosensitizer Bacteria Photodynamic inactivation |
title_short |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
title_full |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
title_fullStr |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
title_full_unstemmed |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
title_sort |
Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative |
dc.creator.none.fl_str_mv |
Spesia, Mariana Belen Durantini, Edgardo Néstor |
author |
Spesia, Mariana Belen |
author_facet |
Spesia, Mariana Belen Durantini, Edgardo Néstor |
author_role |
author |
author2 |
Durantini, Edgardo Néstor |
author2_role |
author |
dc.subject.none.fl_str_mv |
Subphthalocyanine Photosensitizer Bacteria Photodynamic inactivation |
topic |
Subphthalocyanine Photosensitizer Bacteria Photodynamic inactivation |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
A novel chloro[2,9,16(2,9,17)-trikis-4-(N-methylpyridyloxy)]subphthalocyaninnato boron(III) iodide (SubOPc3+) has been synthesized by boron trichloride-induced cyclotrimerization of 4-(4-pyridyloxy)phthalonitrile in 1-chloronaphthalene. This approach produced a regioisomers mixture of chloro[2,9,16(2,9,17)-trikis-4-(pyridyloxy)]subphthalocyaninnato boron(III) (SubOPc) with 19% yield. Exhaustive methylation of SubOPc with methyl iodide yielded 92% of tricationic SubOPc3+. The spectroscopic and photodynamic properties of the SubOPc3+ were compared with its homologous non-charged SubOPc and with subphthalocyanine (SubPc). The cationic SubOPc3+ is essentially aggregated in solution of different solvents and it is partially dissolved as monomer in aqueous sodium dodecyl sulfate (SDS) 2% w/v. The photodynamic effect was strongly dependent of the medium, increasing in an appropriated surrounding microenvironment. The photodynamic inactivation produced by these subphthalocyanines was for first time investigated in vitro on a typical Gram-negative bacterium, Escherichia coli. Cationic SubOPc3+ is rapidly bound to E. coli cells reaching a value of ~2 nmol/106 cells after 5 min of incubation with 4 mM of sensitizer in dark. Photosensitized inactivation of E. coli cellular suspensions by SubOPc3+ exhibits a ~2.5 log decrease of cell survival (99.7 % of cellular inactivation), when the cultures are irradiated for 30 min. The growth of E. coli cells was completely arrested when the cultures were exposed to 8 mM of cationic subphthalocyanine and irradiated, whereas a negligible effect was found for the non-charged SubOPc. Also, SubOPc3+ remains a high activity to inactivate E. coli cells immobilized on agar surfaces. Therefore, the reported results indicate that tricationic subphthalocyanines are interesting photosensitizers with useful antibacterial activity. 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. Centro Científico Tecnológico Conicet - Córdoba; Argentina 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 |
description |
A novel chloro[2,9,16(2,9,17)-trikis-4-(N-methylpyridyloxy)]subphthalocyaninnato boron(III) iodide (SubOPc3+) has been synthesized by boron trichloride-induced cyclotrimerization of 4-(4-pyridyloxy)phthalonitrile in 1-chloronaphthalene. This approach produced a regioisomers mixture of chloro[2,9,16(2,9,17)-trikis-4-(pyridyloxy)]subphthalocyaninnato boron(III) (SubOPc) with 19% yield. Exhaustive methylation of SubOPc with methyl iodide yielded 92% of tricationic SubOPc3+. The spectroscopic and photodynamic properties of the SubOPc3+ were compared with its homologous non-charged SubOPc and with subphthalocyanine (SubPc). The cationic SubOPc3+ is essentially aggregated in solution of different solvents and it is partially dissolved as monomer in aqueous sodium dodecyl sulfate (SDS) 2% w/v. The photodynamic effect was strongly dependent of the medium, increasing in an appropriated surrounding microenvironment. The photodynamic inactivation produced by these subphthalocyanines was for first time investigated in vitro on a typical Gram-negative bacterium, Escherichia coli. Cationic SubOPc3+ is rapidly bound to E. coli cells reaching a value of ~2 nmol/106 cells after 5 min of incubation with 4 mM of sensitizer in dark. Photosensitized inactivation of E. coli cellular suspensions by SubOPc3+ exhibits a ~2.5 log decrease of cell survival (99.7 % of cellular inactivation), when the cultures are irradiated for 30 min. The growth of E. coli cells was completely arrested when the cultures were exposed to 8 mM of cationic subphthalocyanine and irradiated, whereas a negligible effect was found for the non-charged SubOPc. Also, SubOPc3+ remains a high activity to inactivate E. coli cells immobilized on agar surfaces. Therefore, the reported results indicate that tricationic subphthalocyanines are interesting photosensitizers with useful antibacterial activity. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-06 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/241094 Spesia, Mariana Belen; Durantini, Edgardo Néstor; Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative; Elsevier; Dyes and Pigments; 77; 1; 6-2008; 229-237 0143-7208 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/241094 |
identifier_str_mv |
Spesia, Mariana Belen; Durantini, Edgardo Néstor; Synthesis and antibacterial photosensitizing properties of a novel tricationic subphthalocyanine derivative; Elsevier; Dyes and Pigments; 77; 1; 6-2008; 229-237 0143-7208 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0143720807001179 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.dyepig.2007.05.008 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846083360395362304 |
score |
13.22299 |