dc.creatorMonterrubio, Carles
dc.creatorPascual Pasto, Guillem
dc.creatorCano, Francisco
dc.creatorVila Ubach, Monica
dc.creatorManzanares, Alejandro
dc.creatorSchaiquevich, Paula Susana
dc.creatorTornero, Jose A.
dc.creatorSosnik, Alejandro Dario
dc.creatorMora, Jaume
dc.creatorMontero Carcaboso, Angel
dc.date.accessioned2018-04-27T19:37:15Z
dc.date.accessioned2018-11-06T14:39:21Z
dc.date.available2018-04-27T19:37:15Z
dc.date.available2018-11-06T14:39:21Z
dc.date.created2018-04-27T19:37:15Z
dc.date.issued2016-02
dc.identifierMonterrubio, Carles; Pascual Pasto, Guillem; Cano, Francisco; Vila Ubach, Monica; Manzanares, Alejandro; et al.; SN-38-loaded nanofiber matrices for local control of pediatric solid tumors after subtotal resection surgery; Elsevier; Biomaterials; 79; 2-2016; 69-78
dc.identifier0142-9612
dc.identifierhttp://hdl.handle.net/11336/43720
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1888669
dc.description.abstractIn addition to surgery, local tumor control in pediatric oncology requires new treatments as an alternative to radiotherapy. SN-38 is an anticancer drug with proved activity against several pediatric solid tumors including neuroblastoma, rhabdomyosarcoma and Ewing sarcoma. Taking advantage of the extremely low aqueous solubility of SN-38, we have developed a novel drug delivery system (DDS) consisting of matrices made of poly(lactic acid) electrospun polymer nanofibers loaded with SN-38 microcrystals for local release in difficult-to-treat pediatric solid tumors. To model the clinical scenario, we conducted extensive preclinical experiments to characterize the biodistribution of the released SN-38 using microdialysis sampling in vivo. We observed that the drug achieves high concentrations in the virtual space of the surgical bed and penetrates a maximum distance of 2 mm within the tumor bulk. Subsequently, we developed a model of subtotal tumor resection in clinically relevant pediatric patient-derived xenografts and used such models to provide evidence of the activity of the SN-38 DDS to inhibit tumor regrowth. We propose that this novel DDS could represent a potential future strategy to avoid harmful radiation therapy as a primary tumor control together with surgery.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.biomaterials.2015.11.055
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0142961215009655
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectLocal chemotherapy delivery
dc.subjectSN-38Poly(lactic acid) electrospun nanofibers
dc.subjectPediatric solid tumor
dc.subjectPharmacokinetics
dc.subjectMicrodialysis
dc.titleSN-38-loaded nanofiber matrices for local control of pediatric solid tumors after subtotal resection surgery
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución