Mostrar el registro sencillo del ítem
dc.contributor.author | Escobar Ivirico, Jorge Luis | es_ES |
dc.contributor.author | Beaumont, Marco | es_ES |
dc.contributor.author | García Cruz, Dunia Mercedes | es_ES |
dc.contributor.author | Gómez Pinedo, Ulises | es_ES |
dc.contributor.author | Monleón Pradas, Manuel | es_ES |
dc.date.accessioned | 2018-04-19T12:37:12Z | |
dc.date.available | 2018-04-19T12:37:12Z | |
dc.date.issued | 2013 | es_ES |
dc.identifier.issn | 0883-9115 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/100708 | |
dc.description.abstract | [EN] In this study, the toxicity of 4-hydroxytamoxifen (4-OHT) on human Schwann cells (HSCs) was evaluated. Substantial alterations in the cell morphology and viability were observed at 4-OHT concentrations higher than 3 mu g/mL. Therefore, we designed and synthesized a drug-polymer conjugate, based on N-(2-hydroxypropyl)methacrylamide (HPMA) and ethyl acrylate (EA) for delivering 4-OHT to the target tissue without the detrimental consequences of the systemic therapy currently used. The macromer carrier of 4-OHT (MATX), with a functionalization degree of 80%, was synthesized in two steps and verified by H-1-NMR and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectroscopy. MATX was conjugated to the poly(HPMA-co-EA) copolymer network via radical polymerization. The influence of MATX on the physical, chemical, and mechanical properties of poly(HPMA-co-EA-co-MATX) with a ratio of 69/29/2 wt% was compared to those of poly(HPMA-co-EA) networks with a similar feed mixture. The in vitro release of 4-OHT within 1 month was 6 wt% of the total amount of drug linked to the copolymer backbone. | es_ES |
dc.description.sponsorship | This study was financially supported by the Spanish Science & Innovation Ministry through MAT 2011-28791-C03 and PRI-PIMNEU-2011-1372 (ERA-NET call) projects. | en_EN |
dc.language | Inglés | es_ES |
dc.publisher | SAGE Publications | es_ES |
dc.relation.ispartof | Journal of Bioactive and Compatible Polymers | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | 4-Hydroxytamoxifen | es_ES |
dc.subject | Cytotoxicity | es_ES |
dc.subject | Estrogen receptor delivery | es_ES |
dc.subject | Human Schwann cells | es_ES |
dc.subject | Drug-polymer conjugate | es_ES |
dc.subject.classification | MAQUINAS Y MOTORES TERMICOS | es_ES |
dc.title | Cytotoxic effect of 4-hydroxytamoxifen conjugate material on human Schwann cells: Synthesis and characterization | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1177/0883911513506664 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//MAT2011-28791-C03-02/ES/MATERIALES DE SOPORTE Y LIBERACION CONTROLADA PARA LA REGENERACION DE ESTRUCTURAS NEURALES AFECTADAS POR ICTUS/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PRI-PIMNEU-2011-1372/ES/MATERIALES BIFUNCIONALES PARA LA REGENERACION NEURAL DE AREAS AFECTADAS POR ICTUS/ | es_ES |
dc.rights.accessRights | Cerrado | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Termodinámica Aplicada - Departament de Termodinàmica Aplicada | es_ES |
dc.description.bibliographicCitation | Escobar Ivirico, JL.; Beaumont, M.; García Cruz, DM.; Gómez Pinedo, U.; Monleón Pradas, M. (2013). Cytotoxic effect of 4-hydroxytamoxifen conjugate material on human Schwann cells: Synthesis and characterization. Journal of Bioactive and Compatible Polymers. 28(6):574-589. https://doi.org/10.1177/0883911513506664 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1177/0883911513506664 | es_ES |
dc.description.upvformatpinicio | 574 | es_ES |
dc.description.upvformatpfin | 589 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 28 | es_ES |
dc.description.issue | 6 | es_ES |
dc.relation.pasarela | S\262581 | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |