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dc.contributor.authorGrijalvo, Santiago
dc.contributor.authorPuras Ochoa, Gustavo
dc.contributor.authorZarate Sesma, Jon ORCID
dc.contributor.authorSainz Ramos, Myriam
dc.contributor.authorQtaish, Nuseibah A. L.
dc.contributor.authorLópez Méndez, Tania Belén
dc.contributor.authorMashal, Mohamed
dc.contributor.authorAttia, Noha
dc.contributor.authorDíaz Díaz, David
dc.contributor.authorPons, Ramón
dc.contributor.authorFernández, Eduardo
dc.contributor.authorPedraz Muñoz, José Luis ORCID
dc.date.accessioned2019-03-29T12:25:22Z
dc.date.available2019-03-29T12:25:22Z
dc.date.issued2019-02
dc.identifier.citationPharmaceutics 11(2) : (2019) // Article ID 50es_ES
dc.identifier.issn1999-4923
dc.identifier.urihttp://hdl.handle.net/10810/32216
dc.description.abstractCationic niosomes have become important non-viral vehicles for transporting a good number of small drug molecules and macromolecules. Growing interest shown by these colloidal nanoparticles in therapy is determined by their structural similarities to liposomes. Cationic niosomes are usually obtained from the self-assembly of non-ionic surfactant molecules. This process can be governed not only by the nature of such surfactants but also by others factors like the presence of additives, formulation preparation and properties of the encapsulated hydrophobic or hydrophilic molecules. This review is aimed at providing recent information for using cationic niosomes for gene delivery purposes with particular emphasis on improving the transportation of antisense oligonucleotides (ASOs), small interference RNAs (siRNAs), aptamers and plasmids (pDNA).es_ES
dc.description.sponsorshipThis research was funded by the Spanish Ministerio de Ciencia e Innovacion (MICINN), grant numbers CTQ2017-84415-R, MAT2015-69967-C3-1R, CTQ2017-88948-P, CIBER-BBN, grant numbers CB06_ 01_ 0019, CB06_ 01_ 1028 and CB01_ 01_ 1053, by the Basque Country Government, grant number CGIC10/172 and the Generalitat de Catalunya, grant number 2017/SGR/114, 2017/SGR/670.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectantisense oligonucleotideses_ES
dc.subjectaptamerses_ES
dc.subjectcationic lipidses_ES
dc.subjectcationic niosomeses_ES
dc.subjectgene deliveryes_ES
dc.subjectplasmidses_ES
dc.subjectsmall interference RNAes_ES
dc.subjecttherapyes_ES
dc.subjectnonionic surfactant vesicleses_ES
dc.subjectantisense oligonucleotideses_ES
dc.subjectdrug-deliveryes_ES
dc.subjectlipid nanoparticleses_ES
dc.subjecthelper lipidses_ES
dc.subjectbreast-canceres_ES
dc.subjecttransfection efficiencyes_ES
dc.subjectmultidrug-resistancees_ES
dc.subjecttherapeutic deliveryes_ES
dc.subjectsystemic deliveryes_ES
dc.titleCationic Niosomes as Non-Viral Vehicles for Nucleic Acids: Challenges and Opportunities in Gene Deliveryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/1999-4923/11/2/50es_ES
dc.identifier.doi10.3390/pharmaceutics11020050
dc.departamentoesFarmacia y ciencias de los alimentoses_ES
dc.departamentoeuFarmazia eta elikagaien zientziakes_ES


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
Except where otherwise noted, this item's license is described as This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).