Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs
- Autores
- Abraham, Gustavo Abel; Gallardo, Alberto; San Roman, Julio; Fernández Mayoralas, Alfonso; Zurita, Mercedes; Vaquero, Jesús
- Año de publicación
- 2003
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Graft copolymers of poly(ϵ‐caprolactone) (PCL) on poly(dimethylacrylamide) (PDMAm), poly(methylmethacrylate) (PMMA), or on copolymers of poly(DMAm‐co‐MMA) have been synthesized and characterized by 1H NMR spectroscopy, differential scanning calorimetry (DSC), and size exclusion chromatography (SEC). These partially biodegradable copolymer matrices have been proposed as drug delivery systems for the release of low‐molecular‐weight glycosides. Octyl‐N‐acetyl‐6‐O‐[2,2‐bis(hydroxymethyl)‐3‐hydroxypropyl]‐α‐D‐glucosamide, a synthetic carbohydrate able to inhibit the proliferation of human malignant glioma cells in culture and transplanted glioma in rats was selected as drug model. The in vitro aqueous behavior of four drug‐loaded and unloaded graft copolymers of different MMA: DMAm and PCL ratios has been analyzed performing swelling, degradation, and drug release experiments. An intimate dependence of the aqueous behavior with the composition has been found. The higher was the DMAm content, the higher was the hydrophilicity of the synthesized systems as well as the swelling, degradation, and drug release rate. In vivo experiments in pigs demonstrated the very good tolerance of drug‐loaded implanted polymeric discs, and that >95% of the charged drug is released after 2 months' implantation.
Fil: Abraham, Gustavo Abel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España
Fil: Gallardo, Alberto. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España
Fil: San Roman, Julio. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España
Fil: Fernández Mayoralas, Alfonso. Consejo Superior de Investigaciones Científicas; España. Instituto de Química Orgánica General; España
Fil: Zurita, Mercedes. Clínica Puerta de Hierro; España
Fil: Vaquero, Jesús. Clínica Puerta de Hierro; España - Materia
-
Partially Biodegradable Matrices
Graft Copolymers
Antitumoral Drugs
Drug Release
In Vivo Experiments - 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:11336/77591
Ver los metadatos del registro completo
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spelling |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugsAbraham, Gustavo AbelGallardo, AlbertoSan Roman, JulioFernández Mayoralas, AlfonsoZurita, MercedesVaquero, JesúsPartially Biodegradable MatricesGraft CopolymersAntitumoral DrugsDrug ReleaseIn Vivo Experimentshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/2.5https://purl.org/becyt/ford/2Graft copolymers of poly(ϵ‐caprolactone) (PCL) on poly(dimethylacrylamide) (PDMAm), poly(methylmethacrylate) (PMMA), or on copolymers of poly(DMAm‐co‐MMA) have been synthesized and characterized by 1H NMR spectroscopy, differential scanning calorimetry (DSC), and size exclusion chromatography (SEC). These partially biodegradable copolymer matrices have been proposed as drug delivery systems for the release of low‐molecular‐weight glycosides. Octyl‐N‐acetyl‐6‐O‐[2,2‐bis(hydroxymethyl)‐3‐hydroxypropyl]‐α‐D‐glucosamide, a synthetic carbohydrate able to inhibit the proliferation of human malignant glioma cells in culture and transplanted glioma in rats was selected as drug model. The in vitro aqueous behavior of four drug‐loaded and unloaded graft copolymers of different MMA: DMAm and PCL ratios has been analyzed performing swelling, degradation, and drug release experiments. An intimate dependence of the aqueous behavior with the composition has been found. The higher was the DMAm content, the higher was the hydrophilicity of the synthesized systems as well as the swelling, degradation, and drug release rate. In vivo experiments in pigs demonstrated the very good tolerance of drug‐loaded implanted polymeric discs, and that >95% of the charged drug is released after 2 months' implantation.Fil: Abraham, Gustavo Abel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; EspañaFil: Gallardo, Alberto. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; EspañaFil: San Roman, Julio. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; EspañaFil: Fernández Mayoralas, Alfonso. Consejo Superior de Investigaciones Científicas; España. Instituto de Química Orgánica General; EspañaFil: Zurita, Mercedes. Clínica Puerta de Hierro; EspañaFil: Vaquero, Jesús. Clínica Puerta de Hierro; EspañaWiley-liss, Div John Wiley & Sons Inc2003-03-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/77591Abraham, Gustavo Abel; Gallardo, Alberto; San Roman, Julio; Fernández Mayoralas, Alfonso; Zurita, Mercedes; et al.; Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs; Wiley-liss, Div John Wiley & Sons Inc; Journal of Biomedical Materials Research Part A; 64A; 4; 7-3-2003; 638-6471549-32961552-4965CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jbm.a.10297info:eu-repo/semantics/altIdentifier/doi/10.1002/jbm.a.10297info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:34:58Zoai:ri.conicet.gov.ar:11336/77591instacron: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 09:34:58.388CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
title |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
spellingShingle |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs Abraham, Gustavo Abel Partially Biodegradable Matrices Graft Copolymers Antitumoral Drugs Drug Release In Vivo Experiments |
title_short |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
title_full |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
title_fullStr |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
title_full_unstemmed |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
title_sort |
Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs |
dc.creator.none.fl_str_mv |
Abraham, Gustavo Abel Gallardo, Alberto San Roman, Julio Fernández Mayoralas, Alfonso Zurita, Mercedes Vaquero, Jesús |
author |
Abraham, Gustavo Abel |
author_facet |
Abraham, Gustavo Abel Gallardo, Alberto San Roman, Julio Fernández Mayoralas, Alfonso Zurita, Mercedes Vaquero, Jesús |
author_role |
author |
author2 |
Gallardo, Alberto San Roman, Julio Fernández Mayoralas, Alfonso Zurita, Mercedes Vaquero, Jesús |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Partially Biodegradable Matrices Graft Copolymers Antitumoral Drugs Drug Release In Vivo Experiments |
topic |
Partially Biodegradable Matrices Graft Copolymers Antitumoral Drugs Drug Release In Vivo Experiments |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/2.5 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Graft copolymers of poly(ϵ‐caprolactone) (PCL) on poly(dimethylacrylamide) (PDMAm), poly(methylmethacrylate) (PMMA), or on copolymers of poly(DMAm‐co‐MMA) have been synthesized and characterized by 1H NMR spectroscopy, differential scanning calorimetry (DSC), and size exclusion chromatography (SEC). These partially biodegradable copolymer matrices have been proposed as drug delivery systems for the release of low‐molecular‐weight glycosides. Octyl‐N‐acetyl‐6‐O‐[2,2‐bis(hydroxymethyl)‐3‐hydroxypropyl]‐α‐D‐glucosamide, a synthetic carbohydrate able to inhibit the proliferation of human malignant glioma cells in culture and transplanted glioma in rats was selected as drug model. The in vitro aqueous behavior of four drug‐loaded and unloaded graft copolymers of different MMA: DMAm and PCL ratios has been analyzed performing swelling, degradation, and drug release experiments. An intimate dependence of the aqueous behavior with the composition has been found. The higher was the DMAm content, the higher was the hydrophilicity of the synthesized systems as well as the swelling, degradation, and drug release rate. In vivo experiments in pigs demonstrated the very good tolerance of drug‐loaded implanted polymeric discs, and that >95% of the charged drug is released after 2 months' implantation. Fil: Abraham, Gustavo Abel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España Fil: Gallardo, Alberto. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España Fil: San Roman, Julio. Consejo Superior de Investigaciones Científicas; España. Instituto en Ciencia y Tecnología de Polímeros; España Fil: Fernández Mayoralas, Alfonso. Consejo Superior de Investigaciones Científicas; España. Instituto de Química Orgánica General; España Fil: Zurita, Mercedes. Clínica Puerta de Hierro; España Fil: Vaquero, Jesús. Clínica Puerta de Hierro; España |
description |
Graft copolymers of poly(ϵ‐caprolactone) (PCL) on poly(dimethylacrylamide) (PDMAm), poly(methylmethacrylate) (PMMA), or on copolymers of poly(DMAm‐co‐MMA) have been synthesized and characterized by 1H NMR spectroscopy, differential scanning calorimetry (DSC), and size exclusion chromatography (SEC). These partially biodegradable copolymer matrices have been proposed as drug delivery systems for the release of low‐molecular‐weight glycosides. Octyl‐N‐acetyl‐6‐O‐[2,2‐bis(hydroxymethyl)‐3‐hydroxypropyl]‐α‐D‐glucosamide, a synthetic carbohydrate able to inhibit the proliferation of human malignant glioma cells in culture and transplanted glioma in rats was selected as drug model. The in vitro aqueous behavior of four drug‐loaded and unloaded graft copolymers of different MMA: DMAm and PCL ratios has been analyzed performing swelling, degradation, and drug release experiments. An intimate dependence of the aqueous behavior with the composition has been found. The higher was the DMAm content, the higher was the hydrophilicity of the synthesized systems as well as the swelling, degradation, and drug release rate. In vivo experiments in pigs demonstrated the very good tolerance of drug‐loaded implanted polymeric discs, and that >95% of the charged drug is released after 2 months' implantation. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003-03-07 |
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/11336/77591 Abraham, Gustavo Abel; Gallardo, Alberto; San Roman, Julio; Fernández Mayoralas, Alfonso; Zurita, Mercedes; et al.; Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs; Wiley-liss, Div John Wiley & Sons Inc; Journal of Biomedical Materials Research Part A; 64A; 4; 7-3-2003; 638-647 1549-3296 1552-4965 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/77591 |
identifier_str_mv |
Abraham, Gustavo Abel; Gallardo, Alberto; San Roman, Julio; Fernández Mayoralas, Alfonso; Zurita, Mercedes; et al.; Polymeric matrices based on graft copolymers of PCL onto acrylic backbones for releasing antitumoral drugs; Wiley-liss, Div John Wiley & Sons Inc; Journal of Biomedical Materials Research Part A; 64A; 4; 7-3-2003; 638-647 1549-3296 1552-4965 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://onlinelibrary.wiley.com/doi/abs/10.1002/jbm.a.10297 info:eu-repo/semantics/altIdentifier/doi/10.1002/jbm.a.10297 |
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 |
dc.publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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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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1844613086050254848 |
score |
13.070432 |