Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/120733
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dc.creatorGomes, C
dc.creatorLopes, C
dc.creatorLeitner, M
dc.creatorEbner, A
dc.creatorHinterdorfer, P
dc.creatorPêgo, AP
dc.date.accessioned2019-06-25T12:08:38Z-
dc.date.available2019-06-25T12:08:38Z-
dc.date.issued2017
dc.identifier.issn2192-2640
dc.identifier.urihttps://hdl.handle.net/10216/120733-
dc.description.abstractThe ability to design nanoparticle delivery systems capable of selectively target their payloads to specific cell populations is still a major caveat in nanomedicine. One of the main hurdles is the fact that each nanoparticle formulation needs to be precisely tuned to match the specificities of the target cell and route of administration. In this work, molecular recognition force spectroscopy (MRFS) is presented as a tool to evaluate the specificity of neuron-targeted trimethyl chitosan nanoparticles to neuronal cell populations in biological samples of different complexity. The use of atomic force microscopy tips functionalized with targeted or non-targeted nanoparticles made it possible to assess the specific interaction of each formulation with determined cell surface receptors in a precise fashion. More importantly, the combination of MRFS with fluorescent microscopy allowed to probe the nanoparticles vectoring capacity in models of high complexity, such as primary mixed cultures, as well as specific subcellular regions in histological tissues. Overall, this work contributes for the establishment of MRFS as a powerful alternative technique to animal testing in vector design and opens new avenues for the development of advanced targeted nanomedicines.
dc.description.sponsorshipThe authors would like to acknowledge the Bioimaging Center for Biomaterials and Regenerative Therapies of INEB (b.IMAGE) for the support with atomic force and confocal microscopy, Centro de Materiais da Universidade do Porto (CEMUP) for NMR analysis and the Biointerfaces and Nanotechnology Service (INEB-i3S) for nanoparticle size and zeta-potential analysis. The work was financed by Portuguese funds through FCT (Fundação para a Ciência e a Tecnologia) in the framework of the projects UID/BIM/04293/2013, PTDC/CTM-NAN/115124/2009, and PTDC/CTM-NAN/3547/2014. C.P.G. and C.D.F.L. acknowledge FCT for their Ph.D. scholarships SFRH/BD/79930/2011 and SFRH/BD/77933/2011, respectively.
dc.language.isoeng
dc.publisherWiley-VCH Verlag
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147342/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/115124/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F79930%2F2011/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F77933%2F2011/PT
dc.relation.ispartofAdvanced Healthcare Materials, vol. 6(21)
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectatomic force spectroscopy
dc.subjecthistological tissue samples
dc.subjectnanoparticle design
dc.subjectprimary co-cultures
dc.subjecttargeted nanomedicines
dc.titleAtomic Force Microscopy as a Tool to Assess the Specificity of Targeted Nanoparticles in Biological Models of High Complexity
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.1002/adhm.201700597
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/abs/10.1002/adhm.201700597
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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