Sol–gel-based zirconia biocoatings on metal structurally enhanced by polyethylene glycol

For medical components, 316L stainless steel (SS) is widely used. After a period of time, its surface naturally generates a passive oxide layer. Although this layer prevents oxidation or corrosion in an air environment, corrosion still occurs with environmental variation. Thin-film ZrO 2 coatings on...

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Veröffentlicht in:Journal of sol-gel science and technology 2016-03, Vol.77 (3), p.574-584
Hauptverfasser: Lee, Han, Liao, Jiunn-Der, Shao, Pei-Lin, Yao, Chih-Kai, Lin, Yu-Hui, Juang, Yung-Der
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Sprache:eng
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Zusammenfassung:For medical components, 316L stainless steel (SS) is widely used. After a period of time, its surface naturally generates a passive oxide layer. Although this layer prevents oxidation or corrosion in an air environment, corrosion still occurs with environmental variation. Thin-film ZrO 2 coatings on 316L SS deposited using a sol–gel process are a promising solution. In this work, a modified sol–gel process that uses polyethylene glycol as the binding agent was applied to improve the adhesion and reduce the thickness of ZrO 2 coatings on 316L SS. The physical, chemical, and topographical properties of ZrO 2 coatings were evaluated. Human umbilical vein endothelial cells were cultured on ZrO 2 /316L SS and stained with fluorescent dyes to observe their morphology. Then, the 3-(4, 5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS assay) was used to evaluate their proliferation activity on ZrO 2 /316L SS. The pro-inflammatory responses from the cells on ZrO 2 /316L SS were further assessed using the enzyme-linked immunosorbent assay. The results show that an appropriate annealing process is required to remove solvents and additives and to improve the mechanical properties of ZrO 2 coatings. The addition of polyethylene glycol reduces the annealing temperature, enhances the mechanical properties of ZrO 2 coatings, and maintains surface biocompatibility. This paper contributes to the understanding of the cells viability, ZrO 2 sol–gel film cytotoxicity, and 316L SS stainless steel biocompatibility. Graphical Abstract Figure shows that the up-regulation of MCP-1 in HUVECs was time- and dose-dependent. With increasing treatment time, the released concentration of MCP-1 increased. A significant difference among doses became obvious after 4 h of treatment. Hence, the examination of pro-inflammatory responses was performed at 4 h after HUVEC incubation on the samples. The concentration of MCP-1 released by HUVECs cultured on the surface of 316L SS (the control) was higher than those on ZrO 2 /316L SS.
ISSN:0928-0707
1573-4846
DOI:10.1007/s10971-015-3885-z