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dc.contributor.authorVillar Álvarez, Eva María
dc.contributor.authorCambón Freire, Adriana
dc.contributor.authorPardo Montero, Alberto
dc.contributor.authorMosquera Rodríguez, Víctor
dc.contributor.authorBouzas Mosquera, Alberto
dc.contributor.authorTopete Camacho, Antonio
dc.contributor.authorBarbosa Fernández, Silvia
dc.contributor.authorTaboada Antelo, Pablo
dc.contributor.authorMosquera Tallón, Víctor
dc.date.accessioned2020-05-06T07:31:35Z
dc.date.available2020-05-06T07:31:35Z
dc.date.issued2018
dc.identifier.citationVillar-Alvarez, E., Cambón, A., Pardo, A., Mosquera, V., Bouzas-Mosquera, A., Topete, A., Barbosa, S., Taboada, P. and Mosquera, V., 2018. Gold Nanorod-Based Nanohybrids for Combinatorial Therapeutics. ACS Omega, 3(10), pp.12633-12647
dc.identifier.issn2470-1343
dc.identifier.urihttp://hdl.handle.net/10347/22053
dc.description.abstractIn this work, multifunctional nanocarriers consisting of poly(sodium-4-styrenesulfonate) (PSS)/doxorubicin (DOXO)/poly-l-lysine hydrobromide (PLL)/hyaluronic acid (HA)-coated and (PSS/DOXO/PLL)2/HA-coated gold nanorods were assembled by the layer-by-layer technique with the aims of coupling the plasmonic photothermal properties of the metal nanoparticles for plasmonic hyperthermia and the chemoaction of drug DOXO for potential intended combinatorial cancer therapeutics in the future as well as providing different strategies for the controlled and sustained release of the cargo drug molecules. To do that, DOXO could be successfully loaded onto the hybrid nanoconstructs through electrostatic interactions with high efficiencies of up to ca. 78.3 ± 6.9% for the first formed drug layer and 56 ± 13% for the second one, with a total efficiency for the whole system [(PSS/DOXO/PLL)2/HA-coated NRs] of ca. 65.7 ± 1.4%. Nanohybrid internalization was observed to be enhanced by the outer HA layer, which is able to target the CD44 receptors widely overexpressed in some types of cancers as lung, breast, or ovarian ones. Hence, these nanohybrid systems might be versatile nanoplatforms to simultaneously deliver sufficient heat for therapeutic plasmonic hyperthermia and the anticancer drug. Two controlled mechanisms were proposed to modulate the release of the chemodrug, one by means of the enzymatic degradable character of the PLL layer and another by the modulation of the interactions between the polymeric layers through the exploitation of the optical properties of the hybrid particles under near infrared (NIR) laser irradiation. The combination of this bimodal therapeutic approach exerted a synergistic cytotoxic effect on both HeLa and MDA-MB-231 cancer cells in vitro. Cell death mechanisms were also analyzed, elucidating that plasmonic photothermal therapy induces cell necrosis, whereas DOXO activates the cell apoptotic pathway. Therefore, the present NIR laser-induced targeted cancer thermo/chemotherapy represents a novel targeted anticancer strategy with easy control on demand and suitable therapeutic efficacy
dc.description.sponsorshipAuthors thank AIE for funding through Project MAT2016-80266-R. FEDER funds are also greatly acknowledged. E.V.A. and A.P. are grateful to the Spanish Ministerio de Economia y Competitividad for their FPU fellowships
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.rightsCopyright © 2018 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes (https://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
dc.subjectDrug release
dc.subjectLayers
dc.subjectNanoparticles
dc.subjectCells
dc.subjectIrradiation
dc.titleGold Nanorod-Based Nanohybrids for Combinatorial Therapeutics
dc.typeinfo:eu-repo/semantics/article
dc.identifier.DOI10.1021/acsomega.8b01591
dc.relation.publisherversionhttps://doi.org/10.1021/acsomega.8b01591
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Física de Partículas
dc.description.peerreviewedSI


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