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dc.contributor.authorFuentes Paniagua, María Elena 
dc.contributor.authorHernández Ros, José Manuel 
dc.contributor.authorSánchez Milla, María 
dc.contributor.authorCamero, M. Alejandra
dc.contributor.authorMaly, Marek
dc.contributor.authorPérez Serrano, Jorge 
dc.contributor.authorCopa Patiño, José Luis 
dc.contributor.authorSánchez-Nieves Fernández, Javier 
dc.contributor.authorSoliveri de Carranza, Juan 
dc.contributor.authorGómez Ramírez, Rafael 
dc.contributor.authorMata de la Mata, Francisco Javier de la 
dc.date.accessioned2018-07-25T09:19:40Z
dc.date.available2018-07-25T09:19:40Z
dc.date.issued2014-01-01
dc.identifier.bibliographicCitationRSC Advances, 2014, v. 4, p. 1256-1265
dc.identifier.issn2046-2069
dc.identifier.urihttp://hdl.handle.net/10017/33981
dc.description.abstract+ in dendrimer structure have been studied by molecular dynamics. The antibacterial properties of these families of dendrimers have been evaluated against Gram-positive (Staphylococcus aureus CECT 240) and Gram-negative (Escherichia coli CECT 515) bacterial strains, and the results obtained have been compared with those obtained for related cationic carbosilane dendrimers functionalized by hydrosilylation reactions. These data stand out the relevance of the sulfur atom versus the silicon atom close to the dendrimer surface and the outer charge versus the inner charge. Finally, the stability of the most active first generation dendrimers vs. pH and temperature has also been studied.en
dc.description.sponsorshipMinisterio de Economía y Empresaes_ES
dc.description.sponsorshipComunidad de Madrides_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherRoyal Society of Chemistry,en
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)(c) Royal Society of Chemistry, 2013en
dc.rights(c) Royal Society of Chemistry, 2013en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectCationic carbosilane dendrimersen
dc.subjectSulfur atomen
dc.titleCarbosilane cationic dendrimers synthesized by thiol-ene chemistry and their use as antibacterial agentsen
dc.typeinfo:eu-repo/semantics/preprinten
dc.subject.ecienciaQuímicaes_ES
dc.subject.ecienciaChemistryen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Microbiología y Parasitologíaes_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Ciencias Biomédicases_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Biomedicina y Biotecnologíaes_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Orgánica y Química Inorgánicaes_ES
dc.date.updated2018-07-25T09:16:25Z
dc.type.versioninfo:eu-repo/semantics/submittedVersionen
dc.identifier.doi10.1039/C3RA45408H
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//CTQ2011-23245/ES/DISEÑO DE NANOSISTEMAS DENDRITICOS BIFUNCIONALES DE NATURALEZA CARBOSILANO PARA SU APLICACIÓN EN BIOMEDICINAes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/CAM//S2011%2FBMD-2351/ES/Nanosistemas Dendríticos para Aplicaciones Biomédicas - Dendritic Nanosystems for Biomedical Aplicationses_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen
dc.identifier.uxxiAR/0000018822
dc.identifier.publicationtitleRSC Advancesen
dc.identifier.publicationvolume4
dc.identifier.publicationlastpage1265
dc.identifier.publicationfirstpage1256


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Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)(c) Royal Society of Chemistry, 2013
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