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Laser Structured Dental Zirconium for Soft Tissue Cell Occupation—Importance of Wettability Modulation
Authors:Susanne Staehlke  Philip Oster  Susanne Seemann  Fabian Kruse  Jakob Brief  Barbara Nebe
Affiliation:1.Department of Cell Biology, Rostock University Medical Center, 18057 Rostock, Germany; (S.S.); (B.N.);2.Pulsar Photonics GmbH, 52134 Herzogenrath, Germany; (P.O.); (F.K.);3.VITA Zahnfabrik H. Rauter GmbH & Co. KG, 79713 Bad Säckingen, Germany;4.Department Science and Technology of Life, Light and Matter, University of Rostock, 18059 Rostock, Germany
Abstract:Various approaches are being pursued to physico-chemically modify the zirconia neck region of dental implants to improve the integration into the surrounding soft tissue. In this study, polished zirconia discs were laser microstructured with periodic cavities and convex waves. These zirconia samples were additionally activated by argon plasma using the kINPen®09. The surface topography was characterized by scanning electron microscopy and the surface wettability by water contact angle. The in vitro study with human gingival fibroblasts (HGF-1) was focused on cell spreading, morphology, and actin cytoskeleton organization within the first 24 h. The laser-induced microstructures were originally hydrophobic (e.g., 60 µm cavities 138.4°), but after argon plasma activation, the surfaces switched to the hydrophilic state (60 µm cavities 13.7°). HGF-1 cells adhered flatly on the polished zirconia. Spreading is hampered on cavity structures, and cells avoid the holes. However, cells on laser-induced waves spread well. Interestingly, argon plasma activation for only 1 min promoted adhesion and spreading of HGF-1 cells even after 2 h cultivation. The cells crawl and grow into the depth of the cavities. Thus, a combination of both laser microstructuring and argon plasma activation of zirconia seems to be optimal for a strong gingival cell attachment.
Keywords:zirconium   laser micro-structures   cold atmospheric pressure plasma   water contact angle   scanning electron microscopy   in vitro   human gingival cells   cell morphology   actin cytoskeleton   spreading
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