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dc.contributor.authorGiglio, Valentinaen
dc.contributor.authorVarela-Aramburu, Silviaen
dc.contributor.authorTravaglini, Leanaen
dc.contributor.authorFiorini, Federicaen
dc.contributor.authorSeeberger, Peter Hen
dc.contributor.authorMaggini, Lauraen
dc.contributor.authorDe Cola, Luisaen
dc.date.accessioned2019-04-03T14:22:48Z
dc.date.available2019-04-03T14:22:48Z
dc.date.issued2018-05-15en
dc.identifier.issn1385-8947
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/291066
dc.description.abstractThe role played by the shape of mesoporous silica nanoparticles has been investigated for intra- and extracellular delivery. Specifically, we have developed the bottom-up synthesis of flat disc-shaped mesoporous silica nanoparticles, the Nanodiscs (NDs). Due to their peculiar shape and large porous system, NDs present a higher cellular uptake than commonly investigated spherical mesoporous nanoparticles. Moreover, NDs are able to efficiently perform exhaustive delivery of their therapeutic cargo when loaded with the anticancer drug Doxorubicin and administered in vitro to cancerous HeLa cells. Thanks to their aspect ratio, NDs can also be readily assembled into well-organized monolayers to be employed in HeLa cells adhesion experiments upon preliminary functionalization with a specific targeting ligand. In these conditions NDs are able to deliver a hydrophobic dye to adhered cells via the highly accessible vertically aligned pores and their flat surface that ensures optimal cell contact. This initial investigation on the performance of NDs in both intra- and extracellular delivery activities suggests the great potential of these particles.
dc.description.sponsorshipThis work was financially supported by the European Research Council (ERC) Advanced Grant “MAGIC” (grant N° 247365), the Marie Skłodowska-Curie fellowship (MSCA-IEF) “POP-SILICA” (grant N° 627788) and the SACS Project (grant N° 310651), the Foundation ARC through the project “Thera-HCC” (grant N° IHU201301187), the Région Alsace, and the Département du Bas-Rhin. LDC especially acknowledges AXA Research funds. PHS and SVA acknowledge the Max Planck Society for generous funding.
dc.publisherElsevier
dc.titleReshaping Silica Particles: Mesoporous Nanodiscs for Bimodal Delivery and Improved Cellular Uptakeen
dc.typeArticle
prism.endingPage154
prism.publicationDate2018en
prism.publicationNameChemical Engineering Journalen
prism.startingPage148
prism.volume340en
dc.identifier.doi10.17863/CAM.38247
dcterms.dateAccepted2018-01-11en
rioxxterms.versionofrecord10.1016/j.cej.2018.01.059en
rioxxterms.versionVoR*
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
rioxxterms.licenseref.startdate2018-05-15en
dc.contributor.orcidMaggini, Laura [0000-0001-9434-9470]
dc.identifier.eissn1873-3212
rioxxterms.typeJournal Article/Reviewen
cam.issuedOnline2018-01-11en
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1385894718300755?via%3Dihub#!en


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