Carbosilane cationic dendrimers synthesized by thiol-ene chemistry and their use as antibacterial agents
Authors
Fuentes Paniagua, María ElenaIdentifiers
Permanent link (URI): http://hdl.handle.net/10017/33981DOI: 10.1039/C3RA45408H
ISSN: 2046-2069
Publisher
Royal Society of Chemistry,
Date
2014-01-01Affiliation
Universidad de Alcalá. Departamento de Microbiología y Parasitología; Universidad de Alcalá. Departamento de Ciencias Biomédicas; Universidad de Alcalá. Departamento de Biomedicina y Biotecnología; Universidad de Alcalá. Departamento de Química Orgánica y Química InorgánicaFunders
Ministerio de Economía y Empresa
Comunidad de Madrid
Bibliographic citation
RSC Advances, 2014, v. 4, p. 1256-1265
Keywords
Cationic carbosilane dendrimers
Sulfur atom
Project
CTQ2011-23245(Ministerio de Economía y Empresa)
S2011/BMD-2351 (Comunidad de Madrid)
Document type
info:eu-repo/semantics/preprint
Version
info:eu-repo/semantics/submittedVersion
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)(c) Royal Society of Chemistry, 2013
(c) Royal Society of Chemistry, 2013
Access rights
info:eu-repo/semantics/openAccess
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.
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carbosilane_mata_RSC_2014.pdf | 2.207Mb |
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