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dc.contributor.authorCastro Carmona, Javier Servando
dc.date.accessioned2020-12-23T17:56:11Z
dc.date.available2020-12-23T17:56:11Z
dc.date.issued2020-11-16es_MX
dc.identifier.urihttp://cathi.uacj.mx/20.500.11961/15894
dc.description.abstractMethotrexate (MTX) anticancer drug was successfully loaded and released in a controlled manner from polymer micelles made of a diblock copolymer of poly(monomethoxy ethylene glycol)-b-poly(ε-caprolactone) (mPEG-PCL). The empty and MTX-loaded micelles (MTX/mPEG-PCL) were characterized by electron microscopy. The drug release dependence upon pH 5.4, 6.5, and 7.4 for 30 days was proven and characterized by UV-Vis spectroscopy. The cytotoxic effect of MTX/ mPEG-PCL micelles on MCF-7 breast cancer cells was evaluated through an MTT assay. The morphological analysis indicated the successful formation of micelles of 76 and 131 nm for empty and MTX-loaded micelles, respectively. An encapsulation efficiency of 70.2% and a loading capacity of 8.8% were obtained. The in vitro release of MTX showed a gradual and sustained profile over 22 days, with a clear trend to much higher release at acidic pH (80 and 90% for pH 6.7 and 5.5, respectively). The MTX/mPEG-PCL micelles showed an IC50 of MCF-7 cells at 30 µg mL−1 . The results suggested that MTX/mPEG-PCL could be a promising drug delivery system for cancer treatmentes_MX
dc.description.urihttps://doi.org/10.1515/epoly-2020-0064es_MX
dc.language.isoenes_MX
dc.relation.ispartofProducto de investigación IITes_MX
dc.relation.ispartofInstituto de Ingeniería y Tecnologíaes_MX
dc.subjectcancer treatment, copolymer micelles, drug delivery system, encapsulation efficiency, methotrexatees_MX
dc.subject.otherinfo:eu-repo/classification/cti/7es_MX
dc.titlepH-responsive polymer micelles for methotrexate delivery at tumor microenvironmentses_MX
dc.typeArtículoes_MX
dcterms.thumbnailhttp://ri.uacj.mx/vufind/thumbnails/rupiiit.pnges_MX
dcrupi.institutoInstituto de Ingeniería y Tecnologíaes_MX
dcrupi.cosechableSies_MX
dcrupi.norevista1es_MX
dcrupi.volumen20es_MX
dcrupi.nopagina624-635es_MX
dc.identifier.doihttps://doi.org/10.1515/epoly-2020-0064es_MX
dc.journal.titleE-Polymerses_MX
dc.lgacBIOMATERIALES Y SISTEMAS DE LIBERACIÓN DE FÁRMACOSes_MX
dc.cuerpoacademicoCiencia e Ingeniería de Materialeses_MX
dc.contributor.authorexternoCarrillo Castillo, Teresa Darlen
dc.contributor.coauthorexternoLuna Velasco, Antonia
dc.contributor.coauthorexternoZaragoza Contreras, Armando Erasmo


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