The kinetics of the formation of calcium-deficient and carbonated hydroxyapatite at 38°C were investigated by isothermal calorimetry. Hydroxyapatite (HAp) was formed by reaction of the particulate calcium phosphates CaHPO4 and Ca4 (PO4)2O. Compared with its rate of formation in DI water, the formation of calcium-deficient HAp is significantly inhibited in serum. When serum is diluted with DI water, the extent of inhibition varies with the extent of dilution. When collagen or HAp seeds are present the extent of inhibition in serum is reduced. The kinetics of HAp formation were also examined in various concentrations of albumin to establish the extent to which inhibition is associated with the presence of this plasma protein. While HAp formation is inhibited in albumin, the extent of inhibition is not as great as in serum. The formation of carbonated HAp is also inhibited in serum and albumin. However, the extent of inhibition is significantly reduced. The variations in sodium and carbonate in solution during HAp formation indicate that these species are incorporated at different rates, with carbonate incorporation being more rapid. Elevated sodium concentrations in solution result in solution pH values near 12. The reduction in the inhibition of HAp formation may be associated with the reaction to carbonated HAp occurring at elevated pH or with the influence of pH on protein adsorption.
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References
W. F. NEUMAN, Federation Proceedings 28 (1969) 1846.
R. Z. LEGEROS, in “Calcium Phosphates in Oral Biology and Medicine”, edited by H. M. Myers (Krager, Basel, 1991) p. 110.
D. G. A. NELSON, J. Dent. Res. 60(C) (1981) 1621.
D. G. A. NELSON, J. D. B. FEATHERSTONE, J. F. DUNCAN and T. W. CUTRESS, Caries Res. 17 (C) (1983) 200.
F. C. M. DRIESSENS, R. M. H. VERBEECK and H. J. M. HEIJLIGERS, Inorganica Chimica Acta 80 (1983) 19.
M. VIGNOLES, G. BONEL, D. W. HOLCOMB and R. A. YOUNG, Calcif. Tiss. Int. 43 (1988) 33.
B. BLOMBÄCK and L. Å. HANSON (Eds), “Plasma proteins” (Wiley, New York, 1979) p. 20.
G. A. BEKEY and D. D. RENEAU (Eds), “Biomedical engineering principles” (Marcel Dekker, New York, 1976) p. 25.
J. L. MEYER and H. FLEISCH, Mineral Electrolyte Metab. 10 (1984) 249.
A. L. BOSKEY and A. S. POSNER, Mater. Res. Bull. 9 (1974) 907.
N. C. BLUMENTHAL, F. BETTS and A. S. POSNER, Calcif. Tiss. Res. 18 (1975) 81.
P. QUINT, J. ALTHOFF and H. J. HOHLING, Experientia 36 (1980) 151.
G. WILLIAMS and J. D. SALLIS, Calcif. Tiss. Int. 34 (1982) 169.
J. CHRISTOFFERSEN and M. R. CHRISTOFFERSON, J. Cryst. Growth 53 (1981) 42.
K. TENHUISEN and P. W. BROWN, J. Mater. Sci., Materials in Medicine (in press).
M. J. MUHR, S. BEHR and J. C. VOEGEL, J. Biomed. Mater. Res. 23 (1989) 1411.
K. TENHUISEN and P. W. BROWN, Biomim. 1 (1992) 135.
L.-A. ANDERSSON, in “Plasma proteins”, edited by B. Blombäck and L. Å. Hanson (Wiley, New York, 1979) p. 50.
P. W. BROWN, N. HOCKER, and S. HOYLE, J. Amer. Ceram. Soc. 74 (1991) 1848.
M. T. FULMER and P. W. BROWN, J. Biomed. Mater. Res. 27 (1993) 1095.
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Martin, R.I., Brown, P.W. Formation of hydroxyapatite in serum. J Mater Sci: Mater Med 5, 96–102 (1994). https://doi.org/10.1007/BF00121697
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DOI: https://doi.org/10.1007/BF00121697