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dc.contributor.authorIturrioz Rodríguez, Nereaes_ES
dc.contributor.authorGonzález Domínguez, E.es_ES
dc.contributor.authorGonzález Lavado, Eloisaes_ES
dc.contributor.authorMarín Caba, Lauraes_ES
dc.contributor.authorVaz, B.es_ES
dc.contributor.authorPérez Lorenzo, M.es_ES
dc.contributor.authorCorrea Duarte, M.A.es_ES
dc.contributor.authorLópez Fanarraga, Mónica es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2017-11-09T18:28:19Z
dc.date.available2018-10-23T02:45:12Z
dc.date.issued2017-10-23es_ES
dc.identifier.issn1521-3773es_ES
dc.identifier.issn1433-7851es_ES
dc.identifier.urihttp://hdl.handle.net/10902/12302
dc.description.abstractThe translocation of nanomaterials or complex delivery systems into the cytosol is a major challenge in nanobiotechnology. After receptor-mediated endocytosis, most nanomaterials are sequestered and undergo degradation, therapy inactivation, or exocytosis. Herein we explore a novel surface particle coating made of adsorbed carbon nanotubes that provides coated materials with new properties that reproduce the viral cell-invasive mechanisms, namely, receptor-mediated endocytosis, endolysosomal escape, and cytosolic particle release preserving cell viability. This novel biomimetic coating design will enable the intracytoplasmic delivery of many different functional materials endowed with therapeutic, magnetic, optical, or catalytic functionalities, thus opening the door to a wide array of chemical and physical processes within the cytosolic or nuclear domains, and supporting new developments in the biotechnological, pharmaceutical, and biomedical industries.es_ES
dc.format.extent6 p.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rights© John Wiley & Sons. This is the peer reviewed version of the following article: N. Iturrioz-Rodríguez., E. González-Domínguez, E. González-Lavado, L. Marín-Caba, B. Vaz, M. Pérez-Lorenzo, M. A. Correa-Duarte, M. L. Fanarraga, Angew. Chem. Int. Ed. 2017, 56, 13736, which has been published in final form at DOI 10.1002/anie.201707769. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.es_ES
dc.sourceAngewandte Chemie, 2017, 56(44), 13736-13740es_ES
dc.titleA biomimetic escape strategy for cytoplasm invasion by synthetic particleses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1002/anie.201707769
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1002/anie.201707769es_ES
dc.type.versionacceptedVersiones_ES


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