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dc.contributor.authorBramini, Mattia 
dc.contributor.authorYe, Dong
dc.contributor.authorHallerbach, Anna
dc.contributor.authorNic Raghnaill, Michelle
dc.contributor.authorSalvati, Anna
dc.contributor.authorÅberg, Christoffer
dc.contributor.authorDawson, Kenneth A.
dc.date.accessioned2026-02-17T11:03:32Z
dc.date.available2026-02-17T11:03:32Z
dc.date.issued2014-04-28
dc.identifier.citationBramini, Mattia et al. Imaging approach to mechanistic study of nanoparticle interactions with the blood–brain barrier. 2014, ACS nano 8 (5), 4304-4312. DOI: 10.1021/nn5018523es_ES
dc.identifier.urihttps://hdl.handle.net/10481/111087
dc.descriptionFunding for this project has been generously provided by EU FP7 via the small collaborative project NeuroNano (NNP4-SL-2008-214547) and the small collaborative project NanoTransKinetics (NMP4-2010-EU-US-266737); by the INSPIRE (Integrated NanoScience Platform for IREland) program funded by the Irish Government’s Programme for Research in Third Level Institutions, Cycle 4, National Development Plan 2007-2013; and by Science Foundation Ireland (09/RFP/MTR2425). Additionally it is based upon works supported by Science Foundation Ireland (SFI/SRC/B1155 and 12/IA/1422), EU FP7, via the Marie-Curie Initial Training Network PathChooser (PITN-GA-2013-608373) and the ESF Research Networking Programme EpitopeMap.es_ES
dc.description.abstractUnderstanding nanoparticle interactions with the central nervous system, in particular the blood–brain barrier, is key to advances in therapeutics, as well as assessing the safety of nanoparticles. Challenges in achieving insights have been significant, even for relatively simple models. Here we use a combination of live cell imaging and computational analysis to directly study nanoparticle translocation across a human in vitro blood–brain barrier model. This approach allows us to identify and avoid problems in more conventional inferential in vitro measurements by identifying the catalogue of events of barrier internalization and translocation as they occur. Potentially this approach opens up the window of applicability of in vitro models, thereby enabling in depth mechanistic studies in the future. Model nanoparticles are used to illustrate the method. For those, we find that translocation, though rare, appears to take place. On the other hand, barrier uptake is efficient, and since barrier export is small, there is significant accumulation within the barrier.es_ES
dc.description.sponsorshipEU FP7 (NNP4-SL-2008-214547), (NMP4-2010-EU-US-266737)es_ES
dc.description.sponsorshipIrish Government’s Programme for Research in Third Level Institutions INSPIREes_ES
dc.description.sponsorshipScience Foundation Ireland (09/RFP/MTR2425), (SFI/SRC/B1155 and 12/IA/1422)es_ES
dc.description.sponsorshipMarie-Curie Initial Training Network PathChooser (PITN-GA-2013-608373)es_ES
dc.description.sponsorshipESF Research Networking Programme EpitopeMapes_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBlood−brain barrieres_ES
dc.subjectNanoparticleses_ES
dc.subjectTranscytosises_ES
dc.titleImaging approach to mechanistic study of nanoparticle interactions with the blood–brain barrieres_ES
dc.typejournal articlees_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/NNP4-SL-2008-214547es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/NMP4-2010-EU-US-266737es_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/nn5018523
dc.type.hasVersionVoRes_ES


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