Influence of ionic strength and carbonate on the Ca-P coating formation from SBF×5 solution

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Barrere, F. and Blitterswijk van, C.A. and Groot de, K. and Layrolle, P. (2002) Influence of ionic strength and carbonate on the Ca-P coating formation from SBF×5 solution. Biomaterials, 23 (9). pp. 1921-1930. ISSN 0142-9612

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Abstract:Biomimetic calcium-phosphate (Ca-P) coatings were applied on Ti6Al4V by using simulated body fluids concentrated by a factor 5 (SBF×5). The production of SBF×5 solution was possible by decreasing the pH of the solution to approximately 6 using CO2 gas. The subsequent release of this mildly acidic gas led to a pH rise and thus, increasing supersaturation. After immersion for 5 1/2 h a Ca-P coating on Ti6Al4V plates and a precipitate simultaneously formed at pH=6.8. Sodium chloride (NaCl) and hydrogencarbonate (HCO3−) contents were studied in relation to CO2 release and coating formation by changing their individual concentration in SBF×5 solution. On one hand, NaCl-free or low NaCl-content SBF×5 solution led to the earlier aspecific precipitation in the solution than for SBF×5 solution. In contrast, Ca-P coating was formed later and was thinner than the coating obtained in regular SBF×5 solution. High ionic strength delayed precipitation and favored Ca-P heterogeneous nucleation on Ti6Al4V. On the other hand, HCO3− content increased the pH of the solution due to its buffering capacity and influenced the release rate of dissolved CO2. Thus, HCO3− content strongly affected the supersaturation and Ca-P structure. Furthermore, HCO3− favored the attachment of Ca-P mineral on Ti6Al4V by decreasing Ca-P crystal size resulting in a better physical attachment of Ca-P coating on Ti6Al4V substrate.
Item Type:Article
Copyright:© 2002 Elsevier
Faculty:
Science and Technology (TNW)
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Link to this item:http://purl.utwente.nl/publications/74792
Official URL:http://dx.doi.org/10.1016/S0142-9612(01)00318-0
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