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Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses

The effects of testing solutions and conditions on hydroxyapatite (HAp) formation as a means of in vitro bioactivity evaluation of B(2)O(3) containing 45S5 bioactive glasses were systematically investigated. Four glass samples prepared by the traditional melt and quench process, where SiO(2) in 45S5...

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Detalles Bibliográficos
Autores principales: Lu, Xiaonan, Kolzow, Jessica, Chen, Roberto R., Du, Jincheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555879/
https://www.ncbi.nlm.nih.gov/pubmed/31198889
http://dx.doi.org/10.1016/j.bioactmat.2019.05.002
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author Lu, Xiaonan
Kolzow, Jessica
Chen, Roberto R.
Du, Jincheng
author_facet Lu, Xiaonan
Kolzow, Jessica
Chen, Roberto R.
Du, Jincheng
author_sort Lu, Xiaonan
collection PubMed
description The effects of testing solutions and conditions on hydroxyapatite (HAp) formation as a means of in vitro bioactivity evaluation of B(2)O(3) containing 45S5 bioactive glasses were systematically investigated. Four glass samples prepared by the traditional melt and quench process, where SiO(2) in 45S5 was gradually replaced by B(2)O(3) (up to 30%), were studied. Two solutions: the simulated body fluid (SBF) and K(2)HPO(4) solutions were used as the medium for evaluating in vitro bioactivity through the formation of HAp on glass surface as a function of time. It was found that addition of boron oxide delayed the HAp formation in both SBF and K(2)HPO(4) solutions, while the reaction between glass and the K(2)HPO(4) solution is much faster as compared to SBF. In addition to the composition and medium effects, we also studied whether the solution treatments (e.g., adjusting to maintain a pH of 7.4, refreshing solution at certain time interval, and no disturbance during immersion) affect HAp formation. Fourier transform infrared spectrometer (FTIR) equipped with an attenuated total reflection (ATR) sampling technique and scanning electron microscopy (SEM) were conducted to identify HAp formation on glass powder surfaces and to observe HAp morphologies, respectively. The results show that refreshing solution every 24 h produced the fastest HAp formation for low boron-containing samples when SBF was used as testing solution, while no significant differences were observed when K(2)HPO(4) solution was used. This study thus suggests the testing solutions and conditions play an important role on the in vitro bioactivity testing results and should be carefully considered when study materials with varying bioactivities.
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spelling pubmed-65558792019-06-13 Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses Lu, Xiaonan Kolzow, Jessica Chen, Roberto R. Du, Jincheng Bioact Mater Article The effects of testing solutions and conditions on hydroxyapatite (HAp) formation as a means of in vitro bioactivity evaluation of B(2)O(3) containing 45S5 bioactive glasses were systematically investigated. Four glass samples prepared by the traditional melt and quench process, where SiO(2) in 45S5 was gradually replaced by B(2)O(3) (up to 30%), were studied. Two solutions: the simulated body fluid (SBF) and K(2)HPO(4) solutions were used as the medium for evaluating in vitro bioactivity through the formation of HAp on glass surface as a function of time. It was found that addition of boron oxide delayed the HAp formation in both SBF and K(2)HPO(4) solutions, while the reaction between glass and the K(2)HPO(4) solution is much faster as compared to SBF. In addition to the composition and medium effects, we also studied whether the solution treatments (e.g., adjusting to maintain a pH of 7.4, refreshing solution at certain time interval, and no disturbance during immersion) affect HAp formation. Fourier transform infrared spectrometer (FTIR) equipped with an attenuated total reflection (ATR) sampling technique and scanning electron microscopy (SEM) were conducted to identify HAp formation on glass powder surfaces and to observe HAp morphologies, respectively. The results show that refreshing solution every 24 h produced the fastest HAp formation for low boron-containing samples when SBF was used as testing solution, while no significant differences were observed when K(2)HPO(4) solution was used. This study thus suggests the testing solutions and conditions play an important role on the in vitro bioactivity testing results and should be carefully considered when study materials with varying bioactivities. KeAi Publishing 2019-06-05 /pmc/articles/PMC6555879/ /pubmed/31198889 http://dx.doi.org/10.1016/j.bioactmat.2019.05.002 Text en . http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lu, Xiaonan
Kolzow, Jessica
Chen, Roberto R.
Du, Jincheng
Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title_full Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title_fullStr Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title_full_unstemmed Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title_short Effect of solution condition on hydroxyapatite formation in evaluating bioactivity of B(2)O(3) containing 45S5 bioactive glasses
title_sort effect of solution condition on hydroxyapatite formation in evaluating bioactivity of b(2)o(3) containing 45s5 bioactive glasses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555879/
https://www.ncbi.nlm.nih.gov/pubmed/31198889
http://dx.doi.org/10.1016/j.bioactmat.2019.05.002
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