Cui Xu, Zhao Dewei, Zhang Boxun, Gao Yongliang
Department of Orthopaedics, Dalian University Affiliated Zhongshan Hospital, Dalian, China.
J Craniofac Surg. 2009 Sep;20(5):1445-50. doi: 10.1097/SCS.0b013e3181af1529.
A radial segmental defect model of a rabbit was used to study the restoration effect on defects treated with chitosan-coated pressed calcium sulfate pellets combined with recombinant human bone morphogenetic protein-2 (rhBMP-2), coated pressed calcium sulfate pellets, and uncoated pressed calcium sulfate pellets. Nothing was implanted in the control group. After 4, 8, and 12 weeks, the results indicated that coated pressed calcium sulfate pellets combined with rhBMP-2 and coated pressed calcium sulfate pellets facilitated new bone formation on defected bones and that, particularly, the coated pressed calcium sulfate pellets combined with rhBMP-2 was more effective than the coated pressed calcium sulfate pellet. Histologic and tetracycline fluorimetric findings showed that the osteogenesis mechanism of chitosan-coated pressed calcium sulfate pellets is membrane bone formation, and the pellets showed slightly slower resorption that closely coincides with the growth rate of new bone.
采用兔桡骨节段性缺损模型,研究壳聚糖包被的压制硫酸钙颗粒联合重组人骨形态发生蛋白-2(rhBMP-2)、包被的压制硫酸钙颗粒以及未包被的压制硫酸钙颗粒对缺损的修复效果。对照组未植入任何物质。4周、8周和12周后,结果表明,包被的压制硫酸钙颗粒联合rhBMP-2以及包被的压制硫酸钙颗粒促进了缺损骨上新骨的形成,特别是包被的压制硫酸钙颗粒联合rhBMP-2比包被的压制硫酸钙颗粒更有效。组织学和四环素荧光检查结果显示,壳聚糖包被的压制硫酸钙颗粒的成骨机制是膜内成骨,且颗粒的吸收略慢,这与新骨的生长速率密切一致。