Dissolution behavior and in vitro evaluation of sputtered hydroxyapatite films subject to a low temperature hydrothermal treatment
Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as‐sputtered films were hydrothermally recrystallized at 110°C. In immersion tests, the as‐sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermal...
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| Published in | Journal of Biomedical Materials Research Part A Vol. 76A; no. 3; pp. 605 - 613 |
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| Main Authors | , , |
| Format | Journal Article |
| Language | English |
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Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.03.2006
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| ISSN | 1549-3296 1552-4965 |
| DOI | 10.1002/jbm.a.30574 |
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| Abstract | Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as‐sputtered films were hydrothermally recrystallized at 110°C. In immersion tests, the as‐sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3‐E1 osteoblast‐like cells on the as‐sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3‐E1 cells on the as‐sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as‐sputtered film. After a 96‐h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as‐sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3‐E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3‐E1 cells on the as‐sputtered films after a period of 24 h. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006 |
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| AbstractList | Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as‐sputtered films were hydrothermally recrystallized at 110°C. In immersion tests, the as‐sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3‐E1 osteoblast‐like cells on the as‐sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3‐E1 cells on the as‐sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as‐sputtered film. After a 96‐h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as‐sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3‐E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3‐E1 cells on the as‐sputtered films after a period of 24 h. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006 Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the assputtered films were hydrothermally recrystallized at 110DGC. In immersion tests, the as-sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 osteoblast-like cells on the as-sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3-E1 cells on the assputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as-sputtered film. After a 96-h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titaniumsubstrate, and as-sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3-E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3-E1 cells on the as-sputtered films after a period of 24 h. Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as-sputtered films were hydrothermally recrystallized at 110 degrees C. In immersion tests, the as-sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 osteoblast-like cells on the as-sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3-E1 cells on the as-sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as-sputtered film. After a 96-h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as-sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3-E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3-E1 cells on the as-sputtered films after a period of 24 h. Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as-sputtered films were hydrothermally recrystallized at 110 degrees C. In immersion tests, the as-sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 osteoblast-like cells on the as-sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3-E1 cells on the as-sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as-sputtered film. After a 96-h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as-sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3-E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3-E1 cells on the as-sputtered films after a period of 24 h.Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as-sputtered films were hydrothermally recrystallized at 110 degrees C. In immersion tests, the as-sputtered film completely dissolved after 2 days in a culture medium, whereas the thickness of hydrothermally treated films increased with an increase in immersion period, reaching a thickness of 127% after a period of 4 weeks. The proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 osteoblast-like cells on the as-sputtered and hydrothermally treated films were investigated, and the cell morphology was also observed using scanning electron microscopy. The proliferation of MC3T3-E1 cells on the as-sputtered films was suppressed, whereas proliferation on the hydrothermally treated films was comparable to that on control and titanium substrate. The suppression of cell proliferation is associated with an increase in pH of the culture medium caused by dissolution of the as-sputtered film. After a 96-h culture time, the ALP activity of the cells on the hydrothermally treated film was higher than that on the control, titanium substrate, and as-sputtered film samples. From scanning electron microscopic observations, it was found that the MC3T3-E1 cells on the hydrothermally treated films were elongated and had established more intricate filopodia networks with each other, which were also observed for MC3T3-E1 cells on the as-sputtered films after a period of 24 h. |
| Author | Aoki, H. Fukui, Y. Ozeki, K. |
| Author_xml | – sequence: 1 givenname: K. surname: Ozeki fullname: Ozeki, K. email: ozeki@frontier.dendai.ac.jp organization: Frontier Research and Development Center, Tokyo Denki University, Ishizaka, Hatoyama, Hiki, Saitama, 350-0394, Japan – sequence: 2 givenname: H. surname: Aoki fullname: Aoki, H. organization: Frontier Research and Development Center, Tokyo Denki University, Ishizaka, Hatoyama, Hiki, Saitama, 350-0394, Japan – sequence: 3 givenname: Y. surname: Fukui fullname: Fukui, Y. organization: Frontier Research and Development Center, Tokyo Denki University, Ishizaka, Hatoyama, Hiki, Saitama, 350-0394, Japan |
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| CitedBy_id | crossref_primary_10_1007_s10856_007_3288_y crossref_primary_10_3233_BME_151560 crossref_primary_10_3233_BME_230131 crossref_primary_10_1016_j_tsf_2011_04_090 crossref_primary_10_1007_s10856_011_4329_0 crossref_primary_10_1016_j_vacuum_2008_05_019 crossref_primary_10_1016_j_apsusc_2008_08_029 crossref_primary_10_1016_j_tsf_2014_07_058 crossref_primary_10_1002_jbm_b_33347 crossref_primary_10_1007_s12034_008_0140_z crossref_primary_10_3390_jfb13030099 crossref_primary_10_1111_ijac_12145 crossref_primary_10_1177_0885328209340334 |
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| Snippet | Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as‐sputtered films were hydrothermally recrystallized at... Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the as-sputtered films were hydrothermally recrystallized at... Hydroxyapatite (HA) was coated onto titanium substrates using radio frequency sputtering. Some of the assputtered films were hydrothermally recrystallized at... |
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| SubjectTerms | Animals cell culture Cell Proliferation Coated Materials, Biocompatible Crystallization Crystallization - methods Durapatite Hot Temperature hydroxyapatite Materials Testing Materials Testing - methods Mice Microscopy, Electron, Scanning Microscopy, Electron, Scanning - methods Osteoblasts Osteoblasts - physiology Osteoblasts - ultrastructure Prostheses and Implants solubility sputtering Surface Properties Titanium |
| Title | Dissolution behavior and in vitro evaluation of sputtered hydroxyapatite films subject to a low temperature hydrothermal treatment |
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