Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/332715
COMPARTIR / EXPORTAR:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE

Invitar a revisión por pares abierta
Campo DC Valor Lengua/Idioma
dc.contributor.authorPinazo Gassol, Auroraes_ES
dc.contributor.authorAngelet, Martaes_ES
dc.contributor.authorPons Pons, Ramónes_ES
dc.contributor.authorLozano, Marinaes_ES
dc.contributor.authorInfante, María Rosaes_ES
dc.contributor.authorPérez, Lourdeses_ES
dc.date.accessioned2023-08-07T11:02:19Z-
dc.date.available2023-08-07T11:02:19Z-
dc.date.issued2009-07-21-
dc.identifier.citationLangmuir 25(14): 7803-7814 (2009)es_ES
dc.identifier.issn0743-7463-
dc.identifier.urihttp://hdl.handle.net/10261/332715-
dc.description.abstractThe synthesis of a novel class of lysine-based cationic amphiphilic derivatives of the type N(epsilon),N(epsilon)'-bis(n-acyloxypropyl)-l-lysine methyl ester salts combining several hydroxyl functions and aliphatic chains of 12 or 14 carbon atoms is described. The compounds have one, two, three, and four alkyl chains. Aggregation in water was studied by four different methods: surface tension, conductivity, chloride ion activity, and nuclear magnetic resonance ((1)H NMR). The critical aggregation concentration value of the new surfactants depends on both the number of alkyl chains and the alkyl chain length. The formation of vesicles at low concentrations was confirmed by H(1) NMR and optical microscopy. Antimicrobial activity was determined on the basis of the minimum inhibitory concentration (MIC) values. These novel lysine-based surfactants showed moderate antimicrobial activity which may be an important advantage for many biomedical applications.es_ES
dc.description.sponsorshipThis work has been partially supported by the Spanish CICYT under Project CTQ2006-01582.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsclosedAccesses_ES
dc.subjectAlkylses_ES
dc.subjectMoleculeses_ES
dc.subjectMonomerses_ES
dc.subjectPeptides and proteinses_ES
dc.subjectSurfactantses_ES
dc.titleLysine-bisglycidol conjugates as novel lysine cationic surfactantses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1021/la901675p-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1021/la901675pes_ES
dc.identifier.e-issn1520-5827-
dc.contributor.funderComisión Asesora de Investigación Científica y Técnica, CAICYT (España)es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100007272es_ES
dc.identifier.pmid19594174-
dc.identifier.scopus2-s2.0-67651093805-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/67651093805-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
Aparece en las colecciones: (IQAC) Artículos
Ficheros en este ítem:
Fichero Descripción Tamaño Formato
Acceso_restringido.pdf108,79 kBAdobe PDFVista previa
Visualizar/Abrir
Show simple item record

CORE Recommender

PubMed Central
Citations

2
checked on 08-may-2024

SCOPUSTM   
Citations

19
checked on 14-may-2024

WEB OF SCIENCETM
Citations

16
checked on 26-feb-2024

Page view(s)

24
checked on 19-may-2024

Download(s)

15
checked on 19-may-2024

Google ScholarTM

Check

Altmetric

Altmetric


Artículos relacionados:


NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.