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dc.contributor.advisorLópez Fanarraga, Mónica 
dc.contributor.authorIturrioz Rodríguez, Nerea
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2016-09-08T12:12:10Z
dc.date.available2021-07-28T02:45:08Z
dc.date.issued2016-07-27
dc.identifier.urihttp://hdl.handle.net/10902/9025
dc.description.abstractDuring years, different delivery strategies have been used such as viral and non-viral or synthetic vectors. The viral vectors have the advantage that can do a specific receptor-mediated endocytosis and escape lysosomes once are inside cells. But they can cause an immune response, provoke insertional mutagenesis and cannot deliver therapeutic proteins. Synthetic vector such as exosomes or lysosomes, don’t cause immune response and can introduce proteins, but their entry mechanism is no so specific and the efficiency to integrate the cargo is lower. In the view of this, we have investigated the biosynthetic interaction of a new carbon nanotube-coated particle (CCP) for cytoplasmic cargo delivery.es_ES
dc.format.extent36 p.es_ES
dc.language.isoenges_ES
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subject.otherCytoplasmic delivery systemes_ES
dc.subject.otherCCPes_ES
dc.subject.otherSistema de transporte citoplasmáticoes_ES
dc.titleCarbon nanotube coated particles (CCP) for cytoplasmic delivery systemes_ES
dc.typeinfo:eu-repo/semantics/masterThesises_ES
dc.rights.accessRightsopenAccesses_ES
dc.description.degreeMáster en Biología Molecular y Biomedicinaes_ES


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