Real-time protein and cell binding measurements on hydroxyapatite coatings

dc.contributor.authorMartín Vilardell, Anna
dc.contributor.authorCinca i Luis, Núria
dc.contributor.authorJokinen, A.
dc.contributor.authorGarcia Giralt, Natàlia
dc.contributor.authorDosta Parras, Sergi
dc.contributor.authorGarcía Cano, Irene
dc.contributor.authorGuilemany, J. M. (José María)
dc.date.accessioned2020-04-24T15:18:50Z
dc.date.available2020-04-24T15:18:50Z
dc.date.issued2016-09-01
dc.date.updated2020-04-24T15:18:50Z
dc.description.abstractAlthough a lot of in vitro and in vivo assays have been performed during the last few decades years for hydroxyapatite bioactive coatings, there is a lack of exploitation of real-time in vitro interaction measurements. In the present work, real-time interactions for a plasma sprayed hydroxyapatite coating were measured by a Multi-Parametric Surface Plasmon Resonance (MP-SPR), and the results were compared with standard traditional cell viability in vitro assays. MP-SPR is proven to be suitable not only for measurement of molecule-molecule interactions but also molecule-material interaction measurements and cell interaction. Although SPR is extensively utilized in interaction studies, recent research of protein or cell adsorption on hydroxyapatite coatings for prostheses applications was not found. The as-sprayed hydroxyapatite coating resulted in 62.4% of crystalline phase and an average thickness of 24 ± 6 μm. The MP-SPR was used to measure lysozyme protein and human mesenchymal stem cells interaction to the hydroxyapatite coating. A comparison between the standard gold sensor and Hydroxyapatite (HA)-plasma coated sensor denoted a clearly favourable cell attachment on HA coated sensor as a significantly higher signal of cell binding was detected. Moreover, traditional cell viability and proliferation tests showed increased activity with culture time indicating that cells were proliferating on HA coating. Cells show homogeneous distribution and proliferation along the HA surface between one and seven days with no significant mortality. Cells were flattened and spread on rough surfaces from the first day, with increasing cytoplasmatic extensions during the culture time.
dc.format.extent14 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec690719
dc.identifier.issn2079-4983
dc.identifier.pmid27618911
dc.identifier.urihttps://hdl.handle.net/2445/157478
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/jfb7030023
dc.relation.ispartofJournal of Functional Biomaterials , 2016, vol. 7, num. 3
dc.relation.urihttps://doi.org/10.3390/jfb7030023
dc.rightscc-by (c) Martín Vilardell, Anna et al., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Ciència dels Materials i Química Física)
dc.subject.classificationBiosensors
dc.subject.classificationAdsorció
dc.subject.classificationMaterials biomèdics
dc.subject.otherBiosensors
dc.subject.otherAdsorption
dc.subject.otherBiomedical materials
dc.titleReal-time protein and cell binding measurements on hydroxyapatite coatings
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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