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Polymer-Grafted Mesoporous Silica Nanoparticles as Ultrasound-Responsive Drug Carriers

dc.contributor.authorParis, J.L.
dc.contributor.authorCabañas Criado, María Victoria
dc.contributor.authorManzano García, Miguel
dc.contributor.authorVallet Regí, María Dulce Nombre
dc.date.accessioned2023-06-18T05:43:50Z
dc.date.available2023-06-18T05:43:50Z
dc.date.issued2015-09-11
dc.descriptionRESEARCHER ID K-3719-2014 (Miguel Manzano García) ORCID 0000-0001-6238-6111 (Miguel Manzano García) RESEARCHER ID M-3378-2014 (María Vallet Regí) ORCID 0000-0002-6104-4889 (María Vallet Regí) RESEARCHER ID G-8740-2015 (María Victoria Cabañas Criado) ORCID 0000-0002-4753-5665 (María Victoria Cabañas Criado)
dc.description.abstractA new ultrasound-responsive system based on mesoporous silica nanoparticles was developed for biomedical applications, grafting a copolymer on their surface that acts as gatekeeper of the pores. The nanoparticles can be loaded with a cargo at low temperature (4 degrees C), taking advantage of the open conformation that the polymer presents under these conditions. Then, at 37 degrees C the copolymer collapses closing the pore entrances and allowing the nanoparticles to carry the drugs at physiological temperature without premature release, which is of great importance when dealing with cytotoxic drugs in cancer treatments. Upon ultrasound irradiation, the sensitive polymer changes its hydrophobicity and, therefore, its conformation toward coil-like opening the gates and releasing the cargo. These hybrid nanoparticles have been shown to be noncytotoxic and can be internalized into LNCaP cells retaining their ultrasound-responsive capability in the cytoplasm of the cells. Moreover, doxorubicin-loaded hybrid MSNs were incubated with LNCaP cells to show their capacity to induce cell death only when the nanoparticles had been exposed to ultrasound. This work demonstrates that our hybrid-MSNs can be triggered by remote stimuli, which is of capital importance for future applications in drug delivery and cancer therapy.
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.sponsorshipCIBER-BBN
dc.description.sponsorshipVI National RDi Plan
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/41731
dc.identifier.doi10.1021/acsnano.5b04378
dc.identifier.issn1936-0851
dc.identifier.officialurlhttp://pubs.acs.org/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/23183
dc.issue.number11
dc.journal.titleACS Nano
dc.language.isoeng
dc.page.final11033
dc.page.initial11023
dc.publisherAmerican Chemical Society
dc.relation.projectIDMAT2012-35556
dc.relation.projectIDCSO2010-11384-E
dc.relation.projectIDBES-2013-064182
dc.rights.accessRightsopen access
dc.subject.cdu615.46
dc.subject.cdu546
dc.subject.keywordMesoporous silica
dc.subject.keywordUltrasound
dc.subject.keywordStimuli-responsive
dc.subject.keywordDrug delivery
dc.subject.keywordNanomedicine
dc.subject.ucmMateriales
dc.subject.ucmQuímica inorgánica (Química)
dc.subject.unesco3312 Tecnología de Materiales
dc.subject.unesco2303 Química Inorgánica
dc.titlePolymer-Grafted Mesoporous Silica Nanoparticles as Ultrasound-Responsive Drug Carriers
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublication516b56e5-68ed-4717-a469-b4380f555994
relation.isAuthorOfPublication2a7febe9-6dd2-4117-aa12-552e54c12bd3
relation.isAuthorOfPublication791023b8-2531-44eb-ba01-56e3b7caa0cb
relation.isAuthorOfPublication.latestForDiscovery2a7febe9-6dd2-4117-aa12-552e54c12bd3

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