Bone Regeneration Using a Bone Morphogenetic Protein-2 Saturated Slow-Release Gelatin Hydrogel Sheet
Gelatin
DOI:
10.1097/sap.0b013e31819b6c52
Publication Date:
2010-03-18T09:37:42Z
AUTHORS (5)
ABSTRACT
Bone regeneration methods using bone inductive cytokines show promise, however, due to early diffusion and absorption of single applications these cytokines, the effects are limited. In this study, such a system was applied, gelatin hydrogel as carrier slowly release (bone morphogenetic proteins) BMP-2 over relatively long period in vivo. By coupling slow-release with biodegradable copolymer, composite evaluated by grafting into defect sites canine orbital floor fracture model. Radio-iodinated incorporated subcutaneously implanted nude mice showed similar slow (approximately, 60% at 3 days 80% 14 days) radiolabeled alone. contrast, greater than 90% fluid-injected lost injection site within first 8 hours. Using dog model fracture, complex BMP-2-saturated polylactide-based copolymer defect. structural analysis, radiography, histologic examination, microfocus CT, greatly enhanced new formation healing 5 weeks comparison directly saturated same amount (no carrier). A trabecular structure resembling that normal tissue restored generated constructs. Thus study demonstrates potential for difficult defects.
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