Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/34625
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dc.contributor.authorNadine, Sarapt_PT
dc.contributor.authorPatrício, Sónia G.pt_PT
dc.contributor.authorBarrias, Cristina C.pt_PT
dc.contributor.authorChoi, Insung S.pt_PT
dc.contributor.authorMatsusaki, Michiyapt_PT
dc.contributor.authorCorreia, Clara R.pt_PT
dc.contributor.authorMano, João F.pt_PT
dc.date.accessioned2022-09-16T17:11:52Z-
dc.date.available2022-09-16T17:11:52Z-
dc.date.issued2020-11-
dc.identifier.urihttp://hdl.handle.net/10773/34625-
dc.description.abstractA plethora of bioinspired cell-laden hydrogels are being explored as building blocks that once assembled are able to create complex and highly hierarchical structures recapitulating the heterogeneity of living tissues. Yet, the resulting 3D bioengineered systems still present key limitations, mainly related with limited diffusion of essential molecules for cell survival, which dictates the failure of most strategies upon implantation. To maximize the hierarchical complexity of bioengineered systems, while simultaneously fully addressing the exchange efficiency of biomolecules, the high-throughput fabrication of liquefied capsules is proposed using superhydrophobic-superhydrophilic microarrays as platforms to produce the initial structures with high fidelity of geometry and size. The liquefied capsules are composed by i) a permselective multilayered membrane; ii) surface-functionalized poly(ε-caprolactone) microparticles loaded into the liquefied core acting as cell adhesion sites; and iii) cells. It is demonstrated that besides the typical spherical liquefied capsules, it is also possible to obtain multi-shaped blocks with high geometrical precision and efficiency. Importantly, the internal gelation approach used to produce such blocks does not jeopardize cell viability, evidencing the mild conditions of the proposed cell encapsulation technique. The proposed system is intended to be used as hybrid devices implantable using minimally invasive procedures for multiple tissue engineering applications.pt_PT
dc.language.isoengpt_PT
dc.publisherWileypt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_CENTRO/SFRH%2FBD%2F130194%2F2017/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FBTM-MAT%2F31064%2F2017/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FBTM-MAT%2F31210%2F2017/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/669858/EUpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50011%2F2020/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50011%2F2020/PTpt_PT
dc.rightsopenAccesspt_PT
dc.subjectLiquefied capsulespt_PT
dc.subjectModular tissue engineeringpt_PT
dc.subjectMicroparticlespt_PT
dc.subjectStem cellspt_PT
dc.subjectGeometrically-controlled microgelspt_PT
dc.titleGeometrically controlled liquefied capsules for modular tissue engineering strategiespt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.issue11pt_PT
degois.publication.titleAdvanced Biosystemspt_PT
degois.publication.volume4pt_PT
dc.identifier.doi10.1002/adbi.202000127pt_PT
dc.identifier.essn2701-0198-
dc.identifier.articlenumber2000127pt_PT
Appears in Collections:CICECO - Artigos
DQ - Artigos

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