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dc.contributor.authorDeliormanli, AM
dc.date.accessioned2020-07-01T08:29:19Z
dc.date.available2020-07-01T08:29:19Z
dc.date.issuedAUG 1
dc.date.issued2015
dc.identifier.urihttp://hdl.handle.net/20.500.12481/6361
dc.description.abstractIn this study, silicate based 13-93 bioactive glass fibers were prepared through sol-gel processing and electrospinning technique. A precursor solution containing poly (vinyl alcohol) and bioactive glass sol was used to produce fibers. The mixture was electrospun at a voltage of 20 kV by maintaining tip to a collector distance of 10 cm. The amorphous glass fibers with an average diameter of 464 +/- 95 nm were successfully obtained after calcination at 625 degrees C. Hydroxyapatite formation on calcined 13-93 fibers was investigated in simulated body fluid (SBF) using two different fiber concentrations (0.5 and 1 mg/ml) at 37 degrees C. When immesed in SBF, conversion to a calcium phosphate material showed a strong dependence on the fiber concentration. At 1 mg/ml, the surface of the fibers converted to the hydroxyapatite-like material in SBF only after 30 days. At lower solid concentrations (0.5 mg/ml), an amorphous calcium phosphate layer formation was observed followed by the conversion to hydroxyapatite phase after 7 days of immersion. The XIT (2,3-Bis-(2-Methoxy-4-Nitro-5-Sulfopheny1)-2H-Tetrazolium-5-Carboxanilide) assay was conducted to evaluate the osteoblast cell response to the bioactive glass fibers. (C) 2015 Elsevier B.V. All rights reserved.
dc.titlePreparation, in vitro mineralization and osteoblast cell response of electrospun 13-93 bioactive glass nanofibers
dc.title.alternativeMATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
dc.identifier.DOI-ID10.1016/j.msec.2015.04.037
dc.identifier.volume53
dc.identifier.startpage262
dc.identifier.endpage271
dc.identifier.issn/e-issn0928-4931
dc.identifier.issn/e-issn1873-0191


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