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Bioactive Surface Modification of Hydroxyapatite
The purpose of this study was to establish an acid-etching procedure for altering the Ca/P ratio of the nanostructured surface of hydroxyapatite (HAP) by using surface chemical and morphological analyses (XPS, XRD, SEM, surface roughness, and wettability) and to evaluate the in vitro response of ost...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687726/ https://www.ncbi.nlm.nih.gov/pubmed/23862150 http://dx.doi.org/10.1155/2013/626452 |
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author | Abe, Yasuhiko Okazaki, Yohei Hiasa, Kyou Yasuda, Keisuke Nogami, Keisuke Mizumachi, Wataru Hirata, Isao |
author_facet | Abe, Yasuhiko Okazaki, Yohei Hiasa, Kyou Yasuda, Keisuke Nogami, Keisuke Mizumachi, Wataru Hirata, Isao |
author_sort | Abe, Yasuhiko |
collection | PubMed |
description | The purpose of this study was to establish an acid-etching procedure for altering the Ca/P ratio of the nanostructured surface of hydroxyapatite (HAP) by using surface chemical and morphological analyses (XPS, XRD, SEM, surface roughness, and wettability) and to evaluate the in vitro response of osteoblast-like cells (MC3T3-E1 cells) to the modified surfaces. This study utilized HAP and HAP treated with 10%, 20%, 30%, 40%, 50%, or 60% phosphoric acid solution for 10 minutes at 25°C, followed by rinsing 3 times with ultrapure water. The 30% phosphoric acid etching process that provided a Ca/P ratio of 1.50, without destruction of the grain boundary of HAP, was selected as a surface-modification procedure. Additionally, HAP treated by the 30% phosphoric acid etching process was stored under dry conditions at 25°C for 12 hours, and the Ca/P ratio approximated to 1.00 accidentally. The initial adhesion, proliferation, and differentiation (alkaline phosphatase (ALP) activity and relative mRNA level for ALP) of MC3T3-E1 cells on the modified surfaces were significantly promoted (P < 0.05 and 0.01). These findings show that the 30% phosphoric acid etching process for the nanostructured HAP surface can alter the Ca/P ratio effectively and may accelerate the initial adhesion, proliferation, and differentiation of MC3T3-E1 cells. |
format | Online Article Text |
id | pubmed-3687726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36877262013-07-16 Bioactive Surface Modification of Hydroxyapatite Abe, Yasuhiko Okazaki, Yohei Hiasa, Kyou Yasuda, Keisuke Nogami, Keisuke Mizumachi, Wataru Hirata, Isao Biomed Res Int Research Article The purpose of this study was to establish an acid-etching procedure for altering the Ca/P ratio of the nanostructured surface of hydroxyapatite (HAP) by using surface chemical and morphological analyses (XPS, XRD, SEM, surface roughness, and wettability) and to evaluate the in vitro response of osteoblast-like cells (MC3T3-E1 cells) to the modified surfaces. This study utilized HAP and HAP treated with 10%, 20%, 30%, 40%, 50%, or 60% phosphoric acid solution for 10 minutes at 25°C, followed by rinsing 3 times with ultrapure water. The 30% phosphoric acid etching process that provided a Ca/P ratio of 1.50, without destruction of the grain boundary of HAP, was selected as a surface-modification procedure. Additionally, HAP treated by the 30% phosphoric acid etching process was stored under dry conditions at 25°C for 12 hours, and the Ca/P ratio approximated to 1.00 accidentally. The initial adhesion, proliferation, and differentiation (alkaline phosphatase (ALP) activity and relative mRNA level for ALP) of MC3T3-E1 cells on the modified surfaces were significantly promoted (P < 0.05 and 0.01). These findings show that the 30% phosphoric acid etching process for the nanostructured HAP surface can alter the Ca/P ratio effectively and may accelerate the initial adhesion, proliferation, and differentiation of MC3T3-E1 cells. Hindawi Publishing Corporation 2013 2013-06-05 /pmc/articles/PMC3687726/ /pubmed/23862150 http://dx.doi.org/10.1155/2013/626452 Text en Copyright © 2013 Yasuhiko Abe et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Abe, Yasuhiko Okazaki, Yohei Hiasa, Kyou Yasuda, Keisuke Nogami, Keisuke Mizumachi, Wataru Hirata, Isao Bioactive Surface Modification of Hydroxyapatite |
title | Bioactive Surface Modification of Hydroxyapatite |
title_full | Bioactive Surface Modification of Hydroxyapatite |
title_fullStr | Bioactive Surface Modification of Hydroxyapatite |
title_full_unstemmed | Bioactive Surface Modification of Hydroxyapatite |
title_short | Bioactive Surface Modification of Hydroxyapatite |
title_sort | bioactive surface modification of hydroxyapatite |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687726/ https://www.ncbi.nlm.nih.gov/pubmed/23862150 http://dx.doi.org/10.1155/2013/626452 |
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