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Journal of Dental Research, Vol. 82, No. 6, 449-453 (2003)
DOI: 10.1177/154405910308200609

Osteoblast Precursor Cell Attachment on Heat-treated Calcium Phosphate Coatings

Y. Yang1, J.D. Bumgardner2, R. Cavin1, D.L. Carnes3 and J.L Ong1,4,*

1 University of Texas Health Science Center at San Antonio, Department of Restorative Dentistry, Division of Biomaterials, MSC 7890, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900;
2 Mississippi State University, Department of Agricultural and Biological Engineering, Box 9632, Mississippi State, MS 39762;
3 University of Texas Health Science Center at San Antonio, Department of Periodontics, MSC 7894, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900; and
4 University of Texas Health Science Center at San Antonio, Center for Clinical Bioengineering, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900;


Figure 1
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Figure 1. Structural and compositional analysis of CaP coatings of different treatments. (A) Representative x-ray diffraction analyses of as-sputtered Ca coatings, 400°C heat-treated CaP coatings, and 600°C heat-treated CaP coatings. (B) Representative high-resolution O 1s spectra of CaP-coated surfaces by x-ray photoelectron spectroscopy. The O 1s were curve-fitted showing two peaks at 532 eV and 531 eV.

 

Figure 2
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Figure 2. HEPM cell attachment on heat-treated CaP coatings. Data were expressed as the mean ± SD (n = 6). Asterisk (*) indicated significant difference (p < 0.001).

 

Figure 3
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Figure 3. Representative SEM micrographs of attached cell morphology on: (A) control Ti surfaces (X4000), (B) as-sputtered CaP coatings (X4000), (C) 400C heat-treated CaP coatings (X2500), and (D) 600°C heat-treated CaP coatings (X4000). Representative SEM micrographs displaying dividing cells on: (E) control Ti surfaces (X2500), (F) as-depostied CaP coatings (X900), (G) 400°C heat-treated CaP coatings (X2500), and (H) 600°C heat-treated CaP coatings (X2500). Damaged cells were observed on as-sputtered CaP coatings. Bar = 5 µm.

 

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