OBJECTIVE: To evaluate the cytotoxicity of nickel-based alloy surfaces after nitride film coatings. METHODS: A total of 120 disc-shaped specimens (1.5 x 12.0mm) were prepared from nickel (Ni) alloy ingots and metallurgically ground with silicon carbide (SiC) sandpaper to 1200 grit and used as the ground group. Ninety specimens from the ground group were selected and further polished with 1.0 microm aluminum powder slurry and assigned as the polished group. Titanium nitride (TiN) and titanium-aluminum nitride (TiAlN) film coatings were deposited onto 30 polished specimens each by a reactive radio frequency magnetron sputter deposition system and used as coated groups, respectively. The morphological changes and cytoskeleton of tested human gingival fibroblasts were observed using fluorescence microscopy at 3h and 24h time periods, respectively. An MTT assay was used to assess cell viability at 24h. The results were statistically analyzed (n=5, ANOVA, Scheffe', p<0.05). RESULTS: After 3h of incubation, cells began to spread on the test surfaces. Spindle-shaped fibroblasts with well-developed cytoskeleton and distinct actin fibers were observed at the 24h incubation point on the polished and coated specimens. Results of the MTT assay revealed that the TiN and TiAlN film coated groups were significantly higher in cell proliferation and viability than the polished and control groups (p<0.05). SIGNIFICANCE: The biocompatibility of Ni-based alloy was increased significantly after nitride film coating.
OBJECTIVE: To evaluate the cytotoxicity of nickel-based alloy surfaces after nitride film coatings. METHODS: A total of 120 disc-shaped specimens (1.5 x 12.0mm) were prepared from nickel (Ni) alloy ingots and metallurgically ground with silicon carbide (SiC) sandpaper to 1200 grit and used as the ground group. Ninety specimens from the ground group were selected and further polished with 1.0 microm aluminum powder slurry and assigned as the polished group. Titanium nitride (TiN) and titanium-aluminum nitride (TiAlN) film coatings were deposited onto 30 polished specimens each by a reactive radio frequency magnetron sputter deposition system and used as coated groups, respectively. The morphological changes and cytoskeleton of tested human gingival fibroblasts were observed using fluorescence microscopy at 3h and 24h time periods, respectively. An MTT assay was used to assess cell viability at 24h. The results were statistically analyzed (n=5, ANOVA, Scheffe', p<0.05). RESULTS: After 3h of incubation, cells began to spread on the test surfaces. Spindle-shaped fibroblasts with well-developed cytoskeleton and distinct actin fibers were observed at the 24h incubation point on the polished and coated specimens. Results of the MTT assay revealed that the TiN and TiAlN film coated groups were significantly higher in cell proliferation and viability than the polished and control groups (p<0.05). SIGNIFICANCE: The biocompatibility of Ni-based alloy was increased significantly after nitride film coating.
Authors: U Ritz; T Nusselt; A Sewing; T Ziebart; K Kaufmann; A Baranowski; P M Rommens; Alexander Hofmann Journal: Clin Oral Investig Date: 2016-03-12 Impact factor: 3.573
Authors: D M Gordin; T Gloriant; V Chane-Pane; D Busardo; V Mitran; D Höche; C Vasilescu; S I Drob; A Cimpean Journal: J Mater Sci Mater Med Date: 2012-08-24 Impact factor: 3.896
Authors: Jan K Pietruski; Anna Skurska; Anna Bernaczyk; Robert Milewski; Maria Julia Pietruska; Peter Gehrke; Małgorzata D Pietruska Journal: BMC Oral Health Date: 2018-05-02 Impact factor: 2.757