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Antibody-functionalized polymer nanoparticle leading to memory recovery in Alzheimer's disease-like transgenic mouse model

dc.contributor.authorCarradori, Dario
dc.contributor.authorBalducci, Claudia
dc.contributor.authorRe, Francesca
dc.contributor.authorBrambilla, Davide
dc.contributor.authorLe Droumaguet, Benjamin
dc.contributor.authorFlores, Orfeu
dc.contributor.authorGaudin, Alice
dc.contributor.authorMura, Simona
dc.contributor.authorForloni, Gianluigi
dc.contributor.authorOrdóñez Gutiérrez, Lara
dc.contributor.authorWandosell, Francisco
dc.contributor.authorMasserini, Massimo
dc.contributor.authorCouvreur, Patrick
dc.contributor.authorNicolas, Julien
dc.contributor.authorAndrieux,Karine
dc.date.accessioned2025-01-14T10:11:44Z
dc.date.available2025-01-14T10:11:44Z
dc.date.issued2018-02
dc.description.abstractAlzheimer's disease (AD) is a neurodegenerative disorder related, in part, to the accumulation of amyloid-β peptide (Aβ) and especially the Aβ peptide 1-42 (Aβ1-42). The aim of this study was to design nanocarriers able to: (i) interact with the Aβ1-42 in the blood and promote its elimination through the “sink effect” and (ii) correct the memory defect observed in AD-like transgenic mice. To do so, biodegradable, PEGylated nanoparticles were surface-functionalized with an antibody directed against Aβ1-42. Treatment of AD-like transgenic mice with anti-Aβ1-42-functionalized nanoparticles led to: (i) complete correction of the memory defect; (ii) significant reduction of the Aβ soluble peptide and its oligomer level in the brain and (iii) significant increase of the Aβ levels in plasma. This study represents the first example of Aβ1-42 monoclonal antibody-decorated nanoparticle-based therapy against AD leading to complete correction of the memory defect in an experimental model of AD.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationCarradori, D., Balducci, C., Re, F., Brambilla, D., Le Droumaguet, B., Flores, O., Gaudin, A., Mura, S., Forloni, G., Ordoñez-Gutierrez, L., Wandosell, F., Masserini, M., Couvreur, P., Nicolas, J., & Andrieux, K. (2018a). Antibody-functionalized polymer nanoparticle leading to memory recovery in Alzheimer’s disease-like transgenic mouse model. Nanomedicine: Nanotechnology, Biology and Medicine, 14(2), 609-618. https://doi.org/10.1016/j.nano.2017.12.006
dc.identifier.doi10.1016/j.nano.2017.12.006
dc.identifier.issn1549-9634
dc.identifier.officialurlhttps://doi.org/10.1016/J.NANO.2017.12.006
dc.identifier.relatedurlhttps://www.sciencedirect.com/science/article/pii/S1549963417305841?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/20.500.14352/114186
dc.issue.number2
dc.journal.titleNanomedicine: Nanotechnology, Biology and Medicine
dc.language.isoeng
dc.page.final618
dc.page.initial609
dc.publisherElsevier
dc.relation.projectIDnfo:eu-repo/grantAgreement/EC/FP7/2007-2013/212043
dc.rights.accessRightsrestricted access
dc.subject.jel616.894-053.9
dc.subject.keywordPolymer nanoparticles
dc.subject.keywordAlzheimer's disease
dc.subject.keywordAntibody
dc.subject.keywordBlood-brain barrier
dc.subject.keywordβ-Amyloid peptide
dc.subject.ucmNeurociencias (Medicina)
dc.subject.unesco2411.11 Neurofisiología
dc.titleAntibody-functionalized polymer nanoparticle leading to memory recovery in Alzheimer's disease-like transgenic mouse model
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number14
dspace.entity.typePublication
relation.isAuthorOfPublication94711a90-bd22-4a3d-bd83-9a9e13ec2610
relation.isAuthorOfPublication.latestForDiscovery94711a90-bd22-4a3d-bd83-9a9e13ec2610

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