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作 者:陈长青[1] 程高建[2] 练克俭[1] 黄立羡[1] 丁真奇[1] 康两奇[1]
机构地区:[1]厦门大学附属东南医院骨科医院解放军第175医院全军创伤骨科中心,漳州363000 [2]西安医学院西安红十字会医院骨科
出 处:《中华实验外科杂志》2012年第4期732-734,共3页Chinese Journal of Experimental Surgery
基 金:南京军区“十一五”重点计划课题(06229);福建省青年科技人才创新项目(2004F3146)
摘 要:目的观察异种脱蛋白骨(DPB)复合皮质骨来源成骨细胞修复兔桡骨临界骨缺损的效果。方法36只新西兰大白兔的桡骨建立1.5cm临界骨缺损模型,随机分为A、B、C3组,分别植入:A组,异种脱蛋白骨与成骨细胞复合物;B组,自体髂骨;C组,异种脱蛋白骨。术后12周检测如下:X线观察、骨密度测量、标本大体观察、生物力学测试、组织学观察。结果x线显示:A、B两组均可见植入体与桡骨融合,骨折线消失,C组成骨量少,骨折线仍存在。骨密度测量:A、B两组差异无统计学意义(F=2.388,P〉0.05);A、C两组的差异有统计学意义(F=10.869,P〈0.05)。标本大体观察:A、B两组骨折线消失;C组骨折线存在。生物力学测试:A、B组差异无统计学意义(F=1.353,P〉0.05);A、C两组差异有统计学意义(F=4.395,P〈0.05)。组织学观察:A组大量新生骨,B组被周围骨爬行替代,C组少量骨形成。结论异种脱蛋白骨复合成骨细胞可以高效修复兔桡骨临界骨缺损。Objective To evaluate the efficiency of xenogenic deproteinized bone (DPB) based on cortical bone-derived osteoblasts as an alternative in repair of critical bone defect. Methods A total of 36 Newzealand rabbits were randomly divided into groups A, B and C. Critical bone defect with a length of 1.5 cm was created in one side of the radius. The defect was filled with a DPB scaffold seeded with osteo- blasts (group A), autograft (group B) and DPB scaffold (group C ). All specimens were selected for X-ray examination, bone mineral density (BMD) measurements, gross samples observation, biomechanical test and histological observation at 12th week postoperation. Results X-ray examination displayed that the radial defect which was still obvious in group C disappeared in groups A and B. BMD measurements showed that there was no significant differenee in BMD between groups A and B, but that was higher in group C (P 〈0. 05 ). Gross samples observation revealed that the radial defect which was still obvious in group C disappeared in groups A and B. Biomechanical testing demonstrated that the maximum bend load in groups A and B was significantly higher than in group C ( P 〈 0. 05 ). Histologically, there was abundant of newly bone formation in group A, the medullary cavity recanalized in group B, and a small amount of newly bone formation in group C. Conclusion Radial eritieal bone defect could be repaired efficiently by xenogenic DPB based on cortical bone-derived osteoblasts.
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