Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.dental.2016.05.008
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dc.titleGraphene oxide-based substrate: physical and surface characterization, cytocompatibility and differentiation potential of dental pulp stem cells
dc.contributor.authorRosa, Vinicius
dc.contributor.authorXie, Han
dc.contributor.authorDubey, Nileshkumar
dc.contributor.authorMadanagopal, Thulasi T
dc.contributor.authorRajan, Sneha S
dc.contributor.authorMorin, Julien Luc Paul
dc.contributor.authorIslam, Intekhab
dc.contributor.authorNeto, Antonio Helio Castro
dc.date.accessioned2021-08-02T03:50:45Z
dc.date.available2021-08-02T03:50:45Z
dc.date.issued2016-08-01
dc.identifier.citationRosa, Vinicius, Xie, Han, Dubey, Nileshkumar, Madanagopal, Thulasi T, Rajan, Sneha S, Morin, Julien Luc Paul, Islam, Intekhab, Neto, Antonio Helio Castro (2016-08-01). Graphene oxide-based substrate: physical and surface characterization, cytocompatibility and differentiation potential of dental pulp stem cells. DENTAL MATERIALS 32 (8) : 1019-1025. ScholarBank@NUS Repository. https://doi.org/10.1016/j.dental.2016.05.008
dc.identifier.issn01095641
dc.identifier.issn18790097
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/195621
dc.description.abstractObjective The aim of this study was to evaluate the cytotoxicity and differentiation potential of a graphene oxide (GO)-based substrate using dental pulp stem cell (DPSC). Methods GO was obtained via chemical exfoliation of graphite using the modified Hummer's method and dispersed in water-methanol solution. 250 μL of 1.5 mg/mL solution were added to a cover slip and allowed to dry (25 °C, 24 h). GO-based substrate was characterized by Raman spectroscopy, AFM and contact angle. DPSC were seeded on GO and glass (control). Cell attachment and proliferation were evaluated by polymeric F-actin staining, SEM and MTS assay for five days. mRNA expression of MSX-1, PAX-9, RUNX2, COL I, DMP-1 and DSPP were evaluated by qPCR (7 and 14 days). Statistical analyses were performed by either Mann–Whitney, one or two-way Anova followed by and Tukey's post hoc analysis (α = 0.05). Results Peaks at 1587 cm−1 and 1340 cm−1 (G and D band) and ID/IG of 0.83 were observed for GO with Raman. AFM showed that GO was randomly deposited and created a rougher surface comparing to the control. Cells successfully adhered on both substrates. There was no difference in cell proliferation after 5 days. Cells on GO presented higher expression for all genes tested except MSX-1 and RUNX2 for 7 days. Significance GO-based substrate allowed DPSC attachment, proliferation and increased the expression of several genes that are upregulated in mineral-producing cells. These findings open opportunities to the use of GO alone or in combination with dental materials to improve their bioactivity and beyond.
dc.language.isoen
dc.publisherELSEVIER SCI LTD
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectTechnology
dc.subjectDentistry, Oral Surgery & Medicine
dc.subjectMaterials Science, Biomaterials
dc.subjectMaterials Science
dc.subjectCell proliferation
dc.subjectCell differentiation
dc.subjectBioactivity
dc.subjectRaman spectroscopy
dc.subjectSurface characterization
dc.subjectCoating
dc.subjectCarbon
dc.subjectDental pulp stem cells
dc.subjectGRAPHITE OXIDE
dc.typeArticle
dc.date.updated2021-08-01T05:11:52Z
dc.contributor.departmentCENTRE FOR ADVANCED 2D MATERIALS
dc.contributor.departmentDEAN'S OFFICE (DENTISTRY)
dc.contributor.departmentDENTISTRY
dc.contributor.departmentPHYSICS
dc.description.doi10.1016/j.dental.2016.05.008
dc.description.sourcetitleDENTAL MATERIALS
dc.description.volume32
dc.description.issue8
dc.description.page1019-1025
dc.published.statePublished
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