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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/241094

id CONICETDig_14922f184dac59ac98ecaa841ea63532
oai_identifier_str oai:ri.conicet.gov.ar:11336/241094
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling 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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