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Regulating Bone Formation via Controlled Scaffold Degradation
E. Alsberg1,
H.J. Kong2,
Y. Hirano3,
M.K. Smith2,
A. Albeiruti3 and
D.J. Mooney1,2,3,*
1 Departments of Biomedical Engineering,
2 Chemical Engineering, and
3 Biologic and Materials Sciences, Room 5213 Dental School, 1011 North University, University of Michigan, Ann Arbor, MI 48109-1078, USA;

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Figure 2. Transplantation of osteoblasts in alginate with increased degradation rate resulted in qualitatively improved bone formation. Photomicrographs of (A-D) H/E and (E-F) Goldners Trichrome-stained histological sections of tissues formed from primary rat calvarial osteoblasts transplanted in (A,C,E) 0 Mrad 2% alginate-G4RGDSP and (B,D,F) 8 Mrad 2% alginate-G4RGDSP after 6, 13, and 21 wks subcutaneous implantation. [Size bar in photomicrographs represents 200 µm. A = residual alginate, B = bone tissue.]
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Figure 3. Transplantation of osteoblasts in alginate with increased degradation rate resulted in quantitatively improved bone formation. Change in tissue-engineered (A) bone mass, (B) BMC, and (C) BMD over time. (D) Histomorphometric quantification of implant bone fraction over time. [Experimental values are reported as mean (N = 4-5) ± SD. (*) indicates a statistically significant (P < 0.05) difference between irradiated alginate and non-irradiated alginate control at a specific time point.]
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Figure 4. Increased polymer degradation rate results in improved bone microarchitecture as demonstrated by µCT images. µCT image slices of (A) 0 Mrad 2% alginate-G4RGDSP + PRCO and (B) 8 Mrad 2% alginate-G4RGDSP + PRCO after 21 wks. [Image reconstructions are at a resolution of 18 µm; size bars represent 3 mm.]
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Journal of Dental Research, Vol. 82, No. 11,
903-908 (2003)
DOI: 10.1177/154405910308201111

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