Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/35388
Registro completo de metadatos
Campo DC Valor Lengua/Idioma
dc.contributor.authorPalacio Torres, Herman Darío-
dc.contributor.authorOtálvaro Tamayo, Felipe-
dc.contributor.authorGiraldo Morales, Luis Fernando-
dc.contributor.authorPonchel, Gilles-
dc.contributor.authorSegura Sánchez, Freimar-
dc.date.accessioned2023-06-08T19:58:08Z-
dc.date.available2023-06-08T19:58:08Z-
dc.date.issued2017-
dc.identifier.citationPalacio H, Otálvaro F, Giraldo LF, Ponchel G, Segura-Sánchez F. Chitosan-Acrylic Polymeric Nanoparticles with Dynamic Covalent Bonds. Synthesis and Stimuli Behavior. Chem Pharm Bull (Tokyo). 2017 Dec 1;65(12):1132-1143. doi: 10.1248/cpb.c17-00624.spa
dc.identifier.issn0009-2363-
dc.identifier.urihttps://hdl.handle.net/10495/35388-
dc.description.abstractABSTRACT: Drug delivery represents one of the most important research fields within the pharmaceutical industry. Different strategies are reported every day in a dynamic search for carriers with the ability to transport drugs across the body, avoiding or decreasing toxic issues and improving therapeutic activity. One of the most interesting strategies currently under research is the development of drug delivery systems sensitive to different stimuli, due to the high potential attributed to the selective delivery of the payload. In this work, a stimuli-sensitive nanocarrier was built with a bifunctional acrylic polymer, linked by imine and disulfide bonds to thiolate chitosan, the latter being a biopolymer widely known in the field of tissue engineering and drug delivery by its biodegradability and biocompatibility. These polymer nanoparticles were exposed to different changes in pH and redox potential, which are environments commonly found inside cancer cells. The results proof the ability of the nanoparticles to keep the original structure when either changes in pH or redox potential were applied individually. However, when both stimuli were applied simultaneously, a disassembly of the nanoparticles was evident. These special characteristics make these nanoparticles suitable nanocarriers with potential for the selective delivery of anticancer drugs.spa
dc.format.extent12spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherPharmaceutical Society of Japanspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.titleChitosan-Acrylic Polymeric Nanoparticles with Dynamic Covalent Bonds. Synthesis and Stimuli Behaviorspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupBIOPOLIMERspa
dc.publisher.groupSíntesis y Biosíntesis de Metabolitos Naturalesspa
dc.identifier.doi10.1248/cpb.c17-00624-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1347-5223-
oaire.citationtitleChemical and Pharmaceutical Bulletinspa
oaire.citationstartpage1132spa
oaire.citationendpage1143spa
oaire.citationvolume65spa
oaire.citationissue12spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
oaire.fundernameUniversidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIspa
oaire.fundernameDepartamento Administrativo de Ciencia, Tecnología e Innovación, COLCIENCIASspa
oaire.fundernameInstitut Galien Paris Sudspa
dc.publisher.placeTokyo, Japónspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsAntineoplásicos-
dc.subject.decsAntineoplastic Agents - Chemistry-
dc.subject.decsQuitosano - Química-
dc.subject.decsChitosan - Chemistry-
dc.subject.decsDrug Carriers - chemical synthesis-
dc.subject.decsPortadores de Fármacos - Química-
dc.subject.decsDrug Carriers - Chemistry-
dc.subject.decsConcentración de Iones de Hidrógeno-
dc.subject.decsHydrogen-Ion Concentration-
dc.subject.decsEspectroscopía de Resonancia Magnética-
dc.subject.decsMagnetic Resonance Spectroscopy-
dc.subject.decsNanopartículas - Química-
dc.subject.decsNanoparticles - Chemistry-
dc.subject.decsOxidación-Reducción-
dc.subject.decsOxidation-Reduction-
dc.subject.decsTamaño de la Partícula-
dc.subject.decsParticle Size-
dc.subject.decsPolímeros - Química-
dc.subject.decsPolymers - Chemistry-
dc.subject.decsCompuestos de Sulfhidrilo - Química-
dc.subject.decsSulfhydryl Compounds - Chemistry-
dc.description.researchgroupidCOL0065152spa
dc.description.researchgroupidCOL0069689spa
oaire.awardnumber567-2012spa
dc.relation.ispartofjournalabbrevChem. Pharm. Bull.spa
oaire.funderidentifier.rorRoR:03bp5hc83-
oaire.funderidentifier.rorRoR:048jthh02-
oaire.funderidentifier.rorRoR:02mnw9q71-
Aparece en las colecciones: Artículos de Revista en Farmacéutica y Alimentarias

Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
PalacioHerman_2017_Chitosan-Acrylic-Polymeric.pdfArtículo de investigación2.32 MBAdobe PDFVisualizar/Abrir


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons