Cytocompatibility assessment of Ti-Zr-Pd-Si-(Nb) alloys with low Young's modulus, increased hardness, and enhanced osteoblast differentiation for biomedical applications
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
28390183
DOI
10.1002/jbm.b.33892
Knihovny.cz E-resources
- Keywords
- Saos-2 cells, Ti-based alloy, cytocompatibility, osteogenic gene expression, protein adsorption,
- MeSH
- Cell Differentiation drug effects MeSH
- Cell Line MeSH
- Humans MeSH
- Elastic Modulus * MeSH
- Niobium chemistry pharmacology MeSH
- Osteoblasts cytology metabolism MeSH
- Osteogenesis drug effects MeSH
- Palladium chemistry pharmacology MeSH
- Silicones chemistry pharmacology MeSH
- Alloys * chemistry pharmacology MeSH
- Materials Testing * MeSH
- Titanium chemistry pharmacology MeSH
- Zirconium chemistry pharmacology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Niobium MeSH
- Palladium MeSH
- Silicones MeSH
- Alloys * MeSH
- Titanium MeSH
- Zirconium MeSH
Ti-based alloys have increased importance for biomedical applications due to their excellent properties. In particular, the two recently developed TiZrPdSi(Nb) alloys, with a predominant β-Ti phase microstructure, have good mechanical properties, such as a relatively low Young's modulus and high hardness. In the present work, the cytocompatibility of these alloys was assessed using human osteoblast-like Saos-2 cells. Cells grown on the alloys showed larger spreading areas (more than twice) and higher vinculin content (nearly 40% increment) when compared with cells grown on glass control surfaces, indicating a better cell adhesion. Moreover, cell proliferation was 18% higher for cells growing on both alloys than for cells growing on glass and polystyrene control surfaces. Osteogenic differentiation was evaluated by quantifying the expression of four osteogenic genes (osteonectin, osteocalcin, osteopontin, and bone sialoprotein), the presence of three osteogenic proteins (alkaline phosphatase, collagen I, and osteocalcin) and the activity of alkaline phosphatase at different time-points. The results demonstrated that TiZrPdSi and TiZrPdSiNb alloys enhance osteoblast differentiation, and that cells grown on TiZrPdSiNb alloy present higher levels of some late osteogenic markers during the first week in culture. These results suggest that the TiZrPdSi(Nb) alloys can be considered as excellent candidates for orthopaedical uses. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 834-842, 2018.
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