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dc.contributor.authorFuentes Paniagua, María Elena 
dc.contributor.authorSánchez-Nieves Fernández, Javier 
dc.contributor.authorHernández Ros, José Manuel 
dc.contributor.authorFernández Ezequiel, Alba
dc.contributor.authorSoliveri De Carranza, Juan
dc.contributor.authorCopa Patiño, José Luis 
dc.contributor.authorGómez Ramírez, Rafael 
dc.contributor.authorMata de la Mata, Francisco Javier de la 
dc.date.accessioned2018-07-30T09:42:09Z
dc.date.available2018-07-30T09:42:09Z
dc.date.issued2016-01-01
dc.identifier.bibliographicCitationRSC Advances, 2016, v. 6, p. 7022-7033en
dc.identifier.issn2046-2069
dc.identifier.urihttp://hdl.handle.net/10017/34040
dc.description.abstractThis work focuses on the antibacterial activity against Gram-positive Staphylococcus aureus and Gramnegative Escherichia coli and the hemolytic properties of two types of ammonium cationic carbosilane systems: dendrimers and dendrons. The effects of: i) the generation, ii) the type of peripheral groups near the cationic charges (a SiMe2 moiety or a S atom depending on the synthetic procedure, hydrosilylation or thiol-ene addition, respectively), iii) the core of dendrimers (polyphenoxo vs. Si atom) and iv) the focal point of dendrons (-N3, -NH2, -OH) have been assessed. The structure-activity relationship analysis indicates the importance of an adequate balance between the hydrophilic and lipophilic fragments of these molecules to reach the best antibacterial activity. Regarding hemolysis, lowest toxicity values were registered for dendritic systems with a sulfur atom close to the surface and, in the particular case of dendrons, for those with a hydroxyl focal point. One dendrimer and one dendron, both bearing a sulfur atom close to the surface, scored best in the activity-toxicity relationship analysis and were chosen for resistance assays. No changes in the inhibitory and bactericidal capacity in the case of the dendron and only a slight increase of these values for the dendrimer were observed after 15 subculture cycles. Furthermore, these two compounds stayed active towards different strains of resistant bacteria and avoid formation of biofilm at concentrations over the minimum inhibitory concentration (MIC).en
dc.description.sponsorshipMinisterio de Economía y Empresaes_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectDendriticen
dc.subjectCationicen
dc.subjectAntibacterialen
dc.subjectResistance assayen
dc.subjectBiofilmen
dc.titleStructure-activity relationship study of cationic carbosilane dendritic systems as antibacterial agentsen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaChemistryen
dc.subject.ecienciaQuímicaes_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Microbiología y Parasitologíaes_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.updated2018-07-30T09:23:11Z
dc.type.versioninfo:eu-repo/semantics/acceptedVersionen
dc.identifier.doi10.1039/C5RA25901K
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//CTQ2011-23245/ES/DISEÑO DE NANOSISTEMAS DENDRÍTICOS BIFUNCIONALES DE NATURALEZA CARBOSILANO PARA SU APLICACIÓN EN BIOMEDICINAes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen
dc.identifier.uxxiAR/0000023167
dc.identifier.publicationtitleRSC Advancesen
dc.identifier.publicationvolume6
dc.identifier.publicationlastpage7033
dc.identifier.publicationfirstpage7022


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