Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents
- Autores
- Garro, Ariel Gustavo; Alasino, Roxana Valeria; Leonhard, Victoria; Heredia, Valeria; Beltramo, Dante Miguel
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Purpose: The ability of spermidine to increase the selectivity of anticancer agents has been studied extensively. In this research we report the combination of this polyamine and GM1 ganglioside micelles and characterize their behavior for drug delivery.Methods: Dynamic light scattering and electron microscopy were used to characterize size and morphology of micelles. Zeta potential was determined using a Nano-zeta potential analyzer. Sizeexclusion chromatography was used to separate different populations. Cytotoxic effect of micelles was evaluated on Hep2 cell line.Results: Covalent conjugation of spermidine to gangliosides produces a clear reduction of the electronegative z potential of micelle surface. DLS analysis shows no significant differences between both micelles, while TEM image shows a smaller size of Spermidine-GM1.These modified micelles load hydrophilic or hydrophobic antitumor drugs and conjugation does not affect the stability of micelles/drug in solution. Spermidine-GM1/Doxo micelles show faster drug release into cells as compared with GM1/Doxo micelles; however, no evidence can be found for the participation of the polyamine transport system in the uptake of modified micelles.Conclusion: While Spermidine-GM1 and GM1 micelles show similar physical properties, spermidine modified micelles are most efficient to release drugs, making this an interesting alternative to consider for drug delivery.
Fil: Garro, Ariel Gustavo. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina
Fil: Alasino, Roxana Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Leonhard, Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina
Fil: Heredia, Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina
Fil: Beltramo, Dante Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina - Materia
-
SPERMIDINE-GM1 MICELLES
POLYAMINES
DRUG TARGETING
CANCER THERAPY - 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:11336/179628
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oai:ri.conicet.gov.ar:11336/179628 |
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3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral AgentsGarro, Ariel GustavoAlasino, Roxana ValeriaLeonhard, VictoriaHeredia, ValeriaBeltramo, Dante MiguelSPERMIDINE-GM1 MICELLESPOLYAMINESDRUG TARGETINGCANCER THERAPYhttps://purl.org/becyt/ford/2.10https://purl.org/becyt/ford/2Purpose: The ability of spermidine to increase the selectivity of anticancer agents has been studied extensively. In this research we report the combination of this polyamine and GM1 ganglioside micelles and characterize their behavior for drug delivery.Methods: Dynamic light scattering and electron microscopy were used to characterize size and morphology of micelles. Zeta potential was determined using a Nano-zeta potential analyzer. Sizeexclusion chromatography was used to separate different populations. Cytotoxic effect of micelles was evaluated on Hep2 cell line.Results: Covalent conjugation of spermidine to gangliosides produces a clear reduction of the electronegative z potential of micelle surface. DLS analysis shows no significant differences between both micelles, while TEM image shows a smaller size of Spermidine-GM1.These modified micelles load hydrophilic or hydrophobic antitumor drugs and conjugation does not affect the stability of micelles/drug in solution. Spermidine-GM1/Doxo micelles show faster drug release into cells as compared with GM1/Doxo micelles; however, no evidence can be found for the participation of the polyamine transport system in the uptake of modified micelles.Conclusion: While Spermidine-GM1 and GM1 micelles show similar physical properties, spermidine modified micelles are most efficient to release drugs, making this an interesting alternative to consider for drug delivery.Fil: Garro, Ariel Gustavo. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; ArgentinaFil: Alasino, Roxana Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Leonhard, Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; ArgentinaFil: Heredia, Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; ArgentinaFil: Beltramo, Dante Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; ArgentinaBentham Science Publishers2016-03info: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/11336/179628Garro, Ariel Gustavo; Alasino, Roxana Valeria; Leonhard, Victoria; Heredia, Valeria; Beltramo, Dante Miguel; Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents; Bentham Science Publishers; Current Biotechnology; 6; 1; 3-2016; 50-572211-55012211-551XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.eurekaselect.com/openurl/content.php?genre=article&issn=2211-5501&volume=6&issue=1&spage=50info:eu-repo/semantics/altIdentifier/doi/10.2174/2211550105666151228191616info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:51:41Zoai:ri.conicet.gov.ar:11336/179628instacron: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:34982025-09-29 09:51:41.491CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
title |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
spellingShingle |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents Garro, Ariel Gustavo SPERMIDINE-GM1 MICELLES POLYAMINES DRUG TARGETING CANCER THERAPY |
title_short |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
title_full |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
title_fullStr |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
title_full_unstemmed |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
title_sort |
Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents |
dc.creator.none.fl_str_mv |
Garro, Ariel Gustavo Alasino, Roxana Valeria Leonhard, Victoria Heredia, Valeria Beltramo, Dante Miguel |
author |
Garro, Ariel Gustavo |
author_facet |
Garro, Ariel Gustavo Alasino, Roxana Valeria Leonhard, Victoria Heredia, Valeria Beltramo, Dante Miguel |
author_role |
author |
author2 |
Alasino, Roxana Valeria Leonhard, Victoria Heredia, Valeria Beltramo, Dante Miguel |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
SPERMIDINE-GM1 MICELLES POLYAMINES DRUG TARGETING CANCER THERAPY |
topic |
SPERMIDINE-GM1 MICELLES POLYAMINES DRUG TARGETING CANCER THERAPY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.10 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Purpose: The ability of spermidine to increase the selectivity of anticancer agents has been studied extensively. In this research we report the combination of this polyamine and GM1 ganglioside micelles and characterize their behavior for drug delivery.Methods: Dynamic light scattering and electron microscopy were used to characterize size and morphology of micelles. Zeta potential was determined using a Nano-zeta potential analyzer. Sizeexclusion chromatography was used to separate different populations. Cytotoxic effect of micelles was evaluated on Hep2 cell line.Results: Covalent conjugation of spermidine to gangliosides produces a clear reduction of the electronegative z potential of micelle surface. DLS analysis shows no significant differences between both micelles, while TEM image shows a smaller size of Spermidine-GM1.These modified micelles load hydrophilic or hydrophobic antitumor drugs and conjugation does not affect the stability of micelles/drug in solution. Spermidine-GM1/Doxo micelles show faster drug release into cells as compared with GM1/Doxo micelles; however, no evidence can be found for the participation of the polyamine transport system in the uptake of modified micelles.Conclusion: While Spermidine-GM1 and GM1 micelles show similar physical properties, spermidine modified micelles are most efficient to release drugs, making this an interesting alternative to consider for drug delivery. Fil: Garro, Ariel Gustavo. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina Fil: Alasino, Roxana Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Leonhard, Victoria. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina Fil: Heredia, Valeria. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina Fil: Beltramo, Dante Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Provincia de Córdoba. Ministerio de Ciencia y Técnica. Centro de Excelencia en Productos y Procesos de Córdoba; Argentina |
description |
Purpose: The ability of spermidine to increase the selectivity of anticancer agents has been studied extensively. In this research we report the combination of this polyamine and GM1 ganglioside micelles and characterize their behavior for drug delivery.Methods: Dynamic light scattering and electron microscopy were used to characterize size and morphology of micelles. Zeta potential was determined using a Nano-zeta potential analyzer. Sizeexclusion chromatography was used to separate different populations. Cytotoxic effect of micelles was evaluated on Hep2 cell line.Results: Covalent conjugation of spermidine to gangliosides produces a clear reduction of the electronegative z potential of micelle surface. DLS analysis shows no significant differences between both micelles, while TEM image shows a smaller size of Spermidine-GM1.These modified micelles load hydrophilic or hydrophobic antitumor drugs and conjugation does not affect the stability of micelles/drug in solution. Spermidine-GM1/Doxo micelles show faster drug release into cells as compared with GM1/Doxo micelles; however, no evidence can be found for the participation of the polyamine transport system in the uptake of modified micelles.Conclusion: While Spermidine-GM1 and GM1 micelles show similar physical properties, spermidine modified micelles are most efficient to release drugs, making this an interesting alternative to consider for drug delivery. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-03 |
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/11336/179628 Garro, Ariel Gustavo; Alasino, Roxana Valeria; Leonhard, Victoria; Heredia, Valeria; Beltramo, Dante Miguel; Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents; Bentham Science Publishers; Current Biotechnology; 6; 1; 3-2016; 50-57 2211-5501 2211-551X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/179628 |
identifier_str_mv |
Garro, Ariel Gustavo; Alasino, Roxana Valeria; Leonhard, Victoria; Heredia, Valeria; Beltramo, Dante Miguel; Polyamines in the Surface of Lipid Micelles Improve the Cellular Uptake of Antitumoral Agents; Bentham Science Publishers; Current Biotechnology; 6; 1; 3-2016; 50-57 2211-5501 2211-551X CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.eurekaselect.com/openurl/content.php?genre=article&issn=2211-5501&volume=6&issue=1&spage=50 info:eu-repo/semantics/altIdentifier/doi/10.2174/2211550105666151228191616 |
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 |
Bentham Science Publishers |
publisher.none.fl_str_mv |
Bentham Science Publishers |
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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13.070432 |