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Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy
PURPOSE: The aim of the present study was to evaluate the biological response of alkali- and heat-treated titanium-8tantalum-3niobium surfaces by cell proliferation and alkaline phosphatase (ALP) activity analysis. METHODS: Commercial pure titanium (group cp-Ti) and alkali- and heat-treated titanium...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Periodontology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543942/ https://www.ncbi.nlm.nih.gov/pubmed/23346470 http://dx.doi.org/10.5051/jpis.2012.42.6.248 |
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author | Lee, Bo-Ah Kang, Choong-Hee Vang, Mong-Sook Jung, Young-Suk Piao, Xing Hui Kim, Ok-Su Chung, Hyun-Ju Kim, Young-Joon |
author_facet | Lee, Bo-Ah Kang, Choong-Hee Vang, Mong-Sook Jung, Young-Suk Piao, Xing Hui Kim, Ok-Su Chung, Hyun-Ju Kim, Young-Joon |
author_sort | Lee, Bo-Ah |
collection | PubMed |
description | PURPOSE: The aim of the present study was to evaluate the biological response of alkali- and heat-treated titanium-8tantalum-3niobium surfaces by cell proliferation and alkaline phosphatase (ALP) activity analysis. METHODS: Commercial pure titanium (group cp-Ti) and alkali- and heat-treated titanium-8tantalum-3niobium (group AHT) disks were prepared. The surface properties were evaluated using scanning electron microscopy, energy dispersed spectroscopy and X-ray photoelectron spectroscopy (XPS). The surface roughness was evaluated by atomic force microscopy and a profilometer. The contact angle and surface energy were also analyzed. The biological response of fetal rat calvarial cells on group AHT was assessed by cell proliferation and ALP activity. RESULTS: Group AHT showed a flake-like morphology microprofile and dense structure. XPS analysis of group AHT showed an increased amount of oxygen in the basic hydroxyl residue of titanium hydroxide groups compared with group cp-Ti. The surface roughness (Ra) measured by a profilometer showed no significant difference (P>0.05). Group AHT showed a lower contact angle and higher surface energy than group cp-Ti. Cell proliferation on group AHT surfaces was significantly higher than on group cp-Ti surfaces (P<0.05). In comparison to group cp-Ti, group AHT enhanced ALP activity (P<0.05). CONCLUSIONS: These results suggest that group AHT stimulates osteoblast differentiation. |
format | Online Article Text |
id | pubmed-3543942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Academy of Periodontology |
record_format | MEDLINE/PubMed |
spelling | pubmed-35439422013-01-23 Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy Lee, Bo-Ah Kang, Choong-Hee Vang, Mong-Sook Jung, Young-Suk Piao, Xing Hui Kim, Ok-Su Chung, Hyun-Ju Kim, Young-Joon J Periodontal Implant Sci Research Article PURPOSE: The aim of the present study was to evaluate the biological response of alkali- and heat-treated titanium-8tantalum-3niobium surfaces by cell proliferation and alkaline phosphatase (ALP) activity analysis. METHODS: Commercial pure titanium (group cp-Ti) and alkali- and heat-treated titanium-8tantalum-3niobium (group AHT) disks were prepared. The surface properties were evaluated using scanning electron microscopy, energy dispersed spectroscopy and X-ray photoelectron spectroscopy (XPS). The surface roughness was evaluated by atomic force microscopy and a profilometer. The contact angle and surface energy were also analyzed. The biological response of fetal rat calvarial cells on group AHT was assessed by cell proliferation and ALP activity. RESULTS: Group AHT showed a flake-like morphology microprofile and dense structure. XPS analysis of group AHT showed an increased amount of oxygen in the basic hydroxyl residue of titanium hydroxide groups compared with group cp-Ti. The surface roughness (Ra) measured by a profilometer showed no significant difference (P>0.05). Group AHT showed a lower contact angle and higher surface energy than group cp-Ti. Cell proliferation on group AHT surfaces was significantly higher than on group cp-Ti surfaces (P<0.05). In comparison to group cp-Ti, group AHT enhanced ALP activity (P<0.05). CONCLUSIONS: These results suggest that group AHT stimulates osteoblast differentiation. Korean Academy of Periodontology 2012-12 2012-12-31 /pmc/articles/PMC3543942/ /pubmed/23346470 http://dx.doi.org/10.5051/jpis.2012.42.6.248 Text en Copyright © 2012 Korean Academy of Periodontology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/). |
spellingShingle | Research Article Lee, Bo-Ah Kang, Choong-Hee Vang, Mong-Sook Jung, Young-Suk Piao, Xing Hui Kim, Ok-Su Chung, Hyun-Ju Kim, Young-Joon Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title | Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title_full | Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title_fullStr | Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title_full_unstemmed | Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title_short | Surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
title_sort | surface characteristics and osteoblastic cell response of alkali-and heat-treated titanium-8tantalum-3niobium alloy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543942/ https://www.ncbi.nlm.nih.gov/pubmed/23346470 http://dx.doi.org/10.5051/jpis.2012.42.6.248 |
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