Title | Physical profile and impact of a calcium-incorporated implant surface on preosteoblastic cell morphologic and differentiation parameters: A comparative analysis |
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Publication Type | Articolo su Rivista peer-reviewed |
Year of Publication | 2016 |
Authors | Lollobrigida, M., Lamazza L., Capuano C., Formisano G., Serra Emanuele, Laurito D., Romanelli M., Molinari A., and de Biase A. |
Journal | International Journal of Oral and Maxillofacial Implants |
Volume | 31 |
Pagination | 223-231 |
ISSN | 08822786 |
Keywords | 3T3 cell line, 3T3 Cells, Acid Etching, alkaline phosphatase, animal, Animals, Calcium, cell culture technique, Cell Culture Techniques, cell differentiation, cell proliferation, cell shape, chemistry, comparative study, cytology, Dental, dental acid etching, dental etching, dental material, Dental Materials, electron, Interferometry, light, Materials testing, Mice, Microscopy, mouse, Nanomaterial, Nanostructures, osteoblast, Osteoblasts, osteocalcin, physiology, procedures, Scanning, Scanning electron microscopy, Surface properties, surface property, time factor, Time Factors, Titanium |
Abstract | Purpose: To assess and compare topographic features and preosteoblastic cell responses of a new hydrothermally treated, calcium-incorporated surface against other commercially available implant surfaces. Materials and Methods: Four different surfaces were the subject of comparison in this study: machined (MC), resorbable blast media (RBM), sandblasted/large-grit/acid-etched (SLA), and calciumincorporated SLA (Ca-SLA). Surface morphology and roughness were first characterized by scanning electron microscope (SEM) and white light interferometer, respectively. Preosteoblastic MC3T3-E1 cells were then cultured on the titanium surfaces. Cell morphology was observed at 24 hours, 48 hours, 7 days, and 15 days by SEM; differentiation was assessed at 7, 11, and 15 days by assaying alkaline phosphatase (ALP) activity and osteocalcin (OCN) levels. Results: Surface characterization revealed nanotopographic features on Ca-SLA. At topographic analysis, SLA and Ca-SLA showed similar roughness values. Significant differences in cell differentiation parameters were found only at 15 days between the SLA surfaces (both Ca-incorporated and nonincorporated) and MC. Conclusion: Collectively, this study demonstrated that hydrothermal treatment determines the formation of nanotopography without altering the SLA microtopography. Moreover, Ca-SLA and SLA induce MC3T3-E1 cell differentiation at comparable levels. © 2016 by Quintessence Publishing Co Inc. |
Notes | cited By 0 |
URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979093811&doi=10.11607%2fjomi.4247&partnerID=40&md5=d8dc96be128e0261736d07275be0cbf6 |
DOI | 10.11607/jomi.4247 |
Citation Key | Lollobrigida2016223 |