期刊文献+

重组胶原矿化骨负载骨形态发生蛋白2活性多肽复合材料的制备及其异位成骨研究

Preparation of composite of bone based mineralized recombinant collagen loading with BMP2-derived peptide and study on its ectopic osteogenesis
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摘要 目的构建重组胶原矿化骨/BMP2活性多肽新型仿生骨修复材料,并评价其异位成骨能力。方法将48只成年SD大鼠随机分为4组,在A、B、C组的大鼠背部肌肉内分别植入含3、2、1mg BMP2活性多肽的重组胶原矿化骨;在D组的大鼠背部肌肉内植入单纯重组胶原矿化骨,于4、8和12周时间点将大鼠处死,经CT三维重建、组织学观察及钙含量测定检测植入材料的成骨情况。结果A、B、C组,在各时间点的CT三维重建、组织学观察及钙含量检测结果均表明其异位成骨能力优于D组,差异有统计学意义(P〈0.01),其中A、B两组的异位成骨能力优于C组,差异有统计学意义(P〈0.01)。结论BMP2活性多肽可以显著增强重组胶原矿化骨的骨诱导活性,这种骨诱导性存在一定的剂量效应关系。 Objective To prepare a new biomimetic bone matrix material with BMP2-derived peptide combined with bone based mineralized recombinant collagen and investigate its eetopie osteogenetic capacity. Methods Forty-eight adult Sprague-Dawley rats were divided into four groups randomly. Muscle of the rats' back in group A, group B and group C was implanted with bone based mineralized recombinant collagen combined with 3,2,1 mg BMP2-derived peptide, separately. On the week 4,8 and 12 after implantation, the rats were killed and the samples were harvested. Their osteogenic capability was detected by three-dimensional reconstruction of computed tomography, histological observation and content determination of calcium. Results Results Results of three-dimensional reconstruction of computed tomography, histological observation and content determination of calcium indicated that the osteogenie capability of group A, group B and group C was superior to group D with the difference being statistically significant ( P 〈 0.01 ). The osteogenie capability of group A and group B was superior to group C with the difference being statistically significant (P 〈 0.01 ). Conclusion BMP2-derived peptide can increase the osteoinduction of bone based mineralized recombinant collagen and the osteoinduetion has dose-effect relation to some extent.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2008年第12期1655-1656,共2页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金资助项目(30470483) 国家高科技研究发展计划“863”重大项目(2006AA02A124)
关键词 骨形态发生蛋白 胶原 组织工程 BMP2 Collagen Bone Tissue engineering
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参考文献5

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