## Abstract The addition of chondroitin sulphate (CS) to bone cements with calcium phosphate has lead to an enhancement of bone remodeling and an increase in new bone formation in small animals. The goal of this study was to verify the effect of CS in bone cements in a large animal model simulating
Effect of chondroitin sulphate on material properties and bone remodelling around hydroxyapatite/collagen composites
✍ Scribed by Wolfgang Schneiders; Antje Reinstorf; Michael Ruhnow; Sebastian Rehberg; Jan Heineck; Irene Hinterseher; Achim Biewener; Hans Zwipp; Stefan Rammelt
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 725 KB
- Volume
- 85A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
Chondroitin sulphate (CS) has an anti‐inflammatory effect and increases the regeneration ability of injured bone. The goal of this study was to characterize the material properties and osteoconductive potency of calcium phosphate bone cements modified with CS. The early interface reaction of cancellous bone to a nanokristalline hydroxyapatite cement containing type I collagen (HA/Coll) without and with CS (HA/Coll/CS) in a rat tibia model was evaluated. Cylindrical implants were inserted press‐fit into defect of the tibial head. Six specimens per group were analyzed at 2, 4, 7, 14, and 28 days. HA/Coll/CS composite cylinders showed a 15% increase in compressive strength and by investigations with powder X‐ray diffraction more nontransformed cement precursor was found. The microstructures of both types of implants were similar. A significantly higher average number of TRAP positive osteoclasts and ED1 positive mononuclear cells were observed in the interface around HA/Coll/CS implants on day 4 and 7 (p < 0.05). At 28 days the direct bone contact and the percentage of newly formed bone were significantly higher around HA/Coll/CS implants (p < 0.05). The addition of CS appears to enhance bone remodelling and new bone formation around HA/Coll composites in the early stages of bone healing. Possible mechanisms are discussed. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008
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