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Syntheses of Hydroxyapatite Nanospheres Through a Facile Sol-gel Method

Published online by Cambridge University Press:  31 January 2011

Kai Li  and
Sie Chin Tjong
Kai Li
Affiliation:
[email protected], City University of Hong Kong, Physics & Materials Science, Hong Kong, Hong Kong
Sie Chin Tjong
Affiliation:
[email protected], City University of Hong Kong, Physics & Materials Science, Hong Kong, Hong Kong
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Abstract

Hydroxyapatite (HA) nanospheres were synthesized via the sol-gel route in the presence of poly(vinyl alcohol) (PVA). The HA nanospheres were formed from the reaction between (NH4)2HPO4 and CaCl2 in ethanol/PVA sol-gel system, in which ammonia solution (NH3•H2O) was added to adjust the pH of solution. The as-synthesized products were characterized by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), field emission scanning electron microscopy (FE-SEM) and energy-dispersive X-ray spectroscopy (EDAX). XRD patterns and FTIR spectra showed that the HA nanospheres exhibit the crystalline structure and vibration bands of HA. The Ca/P molar ratio of HA nanospheres (50˜70nm) approached the stoichiometric value of 1.67, on the basis of EDAX results. Simulated Body Fluid (SBF) immersion test for three weeks demonstrated that the apatite layer can be formed on the HA nanospheres sintered at 550°C.

Keywords

sol-gelceramicbiomaterial
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 1239: Symposium VV – Micro- and Nanoscale Processing of Biomaterials , 2009 , 1239-VV07-33
Copyright
Copyright © Materials Research Society 2010

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References

[1] Downes, R. N. Vardy, S. and Tanner, K. E. Bioceramics 4, 239 (1991).Google Scholar
[2] Tanner, K. E. Downes, R. N. and Bonfield, W. Br. Ceram. Trans. 93, 104 (1994).Google Scholar
[3] Phillips, M. J. Darr, J. A. Luklinska, Z. B. and Rehman, I. J. Mater. Sci. Mater. Med. 14, 875 (2003).Google Scholar
[4] Lim, G. K. Wang, J. Ng, S. C. Chew, C. H. and Gan, L. M. Biomaterials 18, 1433 (1997).Google Scholar
[5] Chang, M. C. Ko, C. C. and Douglas, W. H. Biomaterials 24, 3087 (2003).Google Scholar
[6] Zhu, P. Y. Masuda and Koumoto, K. Biomaterials 25, 3915 (2004).Google Scholar
[7] Paradosssi, G. Cavalieri, F. Chiessi, E. Spagnoli, C. and Cowman, M. K. J. Mater. Sci. :Mater. Med. 14, 687 (2003).Google Scholar
[8] Sinha, A. Nayar, S. and Agrawak, A. C. J. Am. Ceram. Soc. 86, 357 (2003).Google Scholar
[9] Kokubo, T. and Takadama, H. Biomaterials 27, 2907 (2006).Google Scholar
[10] Zhang, C. M. Yang, J. Quan, Z. W. Yang, P. P. Li, C. X. Hou, Z. Y. and Lin, J. Cryst. Growth Des. 9, 2725 (2009).Google Scholar
[11] Miyaji, F. Kono, Y. and Suyama, Y. Mater. Res. Bull. 40, 209 (2005).Google Scholar
[12] Koutsopoulos, S. J. Biomed. Mater. Res. 62, 600 (2002).Google Scholar
[13] Mollazadeh, S. Javadpour, J. and Khavandi, A. Ceram Intern 33, 1579 (2007).Google Scholar
[14] Wang, F. Li, M. S. Lu, Y. P. and Qi, Y. X. Mater. Lett. 59, 916 (2005).Google Scholar