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Development of Bisphosphonate-Calcium Phosphate Composites and Drug Release Characteristic

Published online by Cambridge University Press:  12 April 2012

Hidekuni Kameda ,
Tomohiko Yoshioka ,
Toshiyuki Ikoma  and
Junzo Tanaka
Hidekuni Kameda
Affiliation:
Department of Metallurgy and Ceramics Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8550 Japan
Tomohiko Yoshioka
Affiliation:
Department of Metallurgy and Ceramics Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8550 Japan
Toshiyuki Ikoma
Affiliation:
Department of Metallurgy and Ceramics Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8550 Japan
Junzo Tanaka
Affiliation:
Department of Metallurgy and Ceramics Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8550 Japan
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Abstract

Bisphosphonate (Bp) was adsorbed on the surface of crystalline calcium phosphates (CP); hydroxyapatite (HAp), octacalcium phosphate (OCP) and Dicalcium phosphate dehydrate (DCPD). The amount of Bp adsorbed was the largest for DCPD per unit surface area, while the amount was the largest for HAp per unit weight. The composites of Bp and amorphous calcium phosphate (ACP) were synthesized by titrating calcium acetate solution into phosphate buffer solution containing Bp. The amount of Bp doped in the composites was 366 μg / mg and was approximately 7 times larger than those of Bp adsorbed on the crystalline Calcium phosphates. TG-DTA measurements of a Bp-calcium and the composite indicated exothermic peaks due to Bp combustion, of which temperature were shifted to higher temperature for the composite. Bp in the composites was gradually released into phosphate buffered saline, while Bp was rapidly released into acetate buffer solution accompanied with the dissolution of ACP. This result suggests that the composite of Bp and ACP has potential for a drug-carrier releasing Bp in response to the condition of osteoclastic bone resorption.

Keywords

Cacompositex-ray diffraction (XRD)
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 1418: Symposium LL/MM – Gels and Biomedical Materials , 2012 , mrsf11-1418-mm10-09
Copyright
Copyright © Materials Research Society 2012

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References

REFERENCES

1. Sakaki, A., Boyce, BF., Cancer research. 55. 3551–3557 (1995).Google Scholar
2. Fleisch, H., Osteoporosis international. 3. 15–22 (1993).Google Scholar
3. Henry Browning, F., Fogler, HS., Lamgmuir. 12. 5231–5238 (1996).CrossRefGoogle Scholar
4. Tarassoff. New england journal of medicine. 353. 2728–2728 (2005).CrossRefGoogle Scholar
5. Ikoma, T. et al. . J. Nanosci. Nanotech, 7, 822–827 (2007).CrossRefGoogle Scholar
6. Koba, M.. Acta poloniae pharmaceutica. 65. 289–294 (2008).Google Scholar
7. Ito, A., Senda, K., Biomed. Mater. 1, 134–139 (2006).CrossRefGoogle Scholar
8. Ohta, K., Monma, H.. Takahashi, S., Journal of the ceramic society of Japan. 107. 577–581 (1999).CrossRefGoogle Scholar
9. Nancolla, GH., Mohan, MS., Archives of oral biology. 15. 731 (1970).CrossRefGoogle Scholar