Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/43001

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dc.contributor.authorPedrosa, Sílvia Santospor
dc.contributor.authorPereira, Paula Alexandra Cunhapor
dc.contributor.authorCorreia, Alexandrapor
dc.contributor.authorMoreira, Susanapor
dc.contributor.authorRocha, Huhopor
dc.contributor.authorGama, F. M.por
dc.date.accessioned2016-11-14T09:52:09Z-
dc.date.available2016-11-14T09:52:09Z-
dc.date.issued2016-
dc.date.submitted2016-
dc.identifier.citationPedrosa, Sílvia S.; Pereira, Paula; Correia, Alexandre; Moreira, Susana; Rocha, H.; Gama, F. M., Biocompatibility of a self-assembled crosslinkable hyaluronic acid nanogel. Macromolecular Bioscience, 16(11), 1610-1620, 2016por
dc.identifier.issn1616-5187por
dc.identifier.urihttps://hdl.handle.net/1822/43001-
dc.description.abstractHyaluronic acid nanogel (HyA-AT) is a redox sensitive crosslinkable nanogel, obtained through the conjugation of a thiolated hydrophobic molecule to the hyaluronic acid chain. Engineered nanogel was studied for its biocompatibility, including immunocompatibility and hemocompatability. The nanogel did not compromise the metabolic activity or cellular membrane integrity of 3T3, microvascular endothelial cells, and RAW 264.7 cell lines, as determined by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide and lactate dehydrogenase release assays. Also, we didn't observe any apoptotic effect on these cell lines through the Annexin V-FITC test. Furthermore, the nanogel cell internalization was analyzed using murine bone marrow derived macrophages, and the in vivo and ex vivo biodistribution of the Cy5.5 labeled nanogel was monitored using a non-invasive near-infrared fluorescence imaging system. The HyA-AT nanogel exhibits fairly a long half-live in the blood stream, thus showing potential for drug delivery applications.por
dc.description.sponsorshipThe authors thank the FCT Strategic Project of UID/BIO/04469/2013 unit, the project RECI/ BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462) and the Project “BioHealth – Biotechnology and Bioengineering approaches to improve health quality”, Ref. NORTE-07-0124- FEDER-000027, co-funded by the Programa Operacional Regional do Norte (ON.2 – O Novo Norte), QREN, FEDER. The authors would like to acknowledge also the support of FCT for the PhD grant reference SFRH/BD/61516/2009. They would also like to thank Bioimaging department on Molecular Medicine Institute (IMM) in Lisbon, namely Dr José Rino and Dr António Temudo. Also thank the animal facilities in IMM (Lisbon), specially Dr. Dolores Bonaparte and Dr. Joana Marques. Finally, the authors thank Dr Africa Gonzalez and Mercedes Pelletero the performance of the studies on the activation of complement.por
dc.language.isoengpor
dc.publisherJohn Wiley and Sonspor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147337/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/126270/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F61516%2F2009/PTpor
dc.rightsopenAccesspor
dc.subjectBiocompatibilitypor
dc.subjectBiodistributionpor
dc.subjectHyaluronic acidpor
dc.subjectImmunocompatibilitypor
dc.subjectNanogelpor
dc.titleBiocompatibility of a self-assembled crosslinkable hyaluronic acid nanogelpor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-5195por
dc.commentsCEB40094por
sdum.publicationstatusinfo:eu-repo/semantics/publishedVersionpor
oaire.citationStartPage1610por
oaire.citationEndPage1620por
oaire.citationIssue11por
oaire.citationConferencePlaceUnited Kingdom-
oaire.citationTitleMacromolecular Biosciencepor
oaire.citationVolume16por
dc.date.updated2016-11-13T18:44:03Z-
dc.identifier.eissn1616-5195-
dc.identifier.doi10.1002/mabi.201600221por
dc.identifier.pmid27456215por
dc.subject.wosScience & Technologypor
sdum.journalMacromolecular Biosciencepor
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