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作 者:王德春[1,2] 陈峥嵘[1,2] 宋后燕[1,2] 彭鲁英[1,2] 费琴明[1,2] 姜南春[1,2]
机构地区:[1]上海医科大学附属中山医院骨科 [2]上海医科大学分子遗传研究室
出 处:《中华创伤杂志》1997年第4期228-231,共4页Chinese Journal of Trauma
摘 要:目的:应用聚乙醇酸(PGA)负载的兔软骨细胞培养移植修复同种异体关节软骨缺损.方法:应用在生物体内可降解吸收、纤维状多孔态的PGA作为支架行兔软骨细胞培养.培养14天后,软骨细胞在PGA提供的三维空间中大量分裂、增殖并合成大量软骨基质,形成PGA-软骨细胞复合体,然后利用该复合体移植修复同种异体兔膝关节全层软骨缺损,对侧膝关节作对照.术后行大体、组织学、电镜动态观察及修复组织厚度测定.结果:PGA在术后8周完全降解吸收,实验侧与对照侧修复组织的厚度有显著性差异(P<0.01);术后16周在实验侧可见典型的软骨组织,电镜下为成熟的软骨细胞,而对照侧为纤维组织修复.结论:应用PGA-软骨细胞复合体移植,可修复同种异体的兔关节软骨缺损,为临床治疗关节软骨缺损奠定了基础.Aim: In an attempt to repair the defects of rabbit articular cartilage with the method of polyglycolic acid (PGA) engineered, cultured chondrocytes homotransplantaion. Methods: The biodegradable, fibrous, multiple microhole PGA was used as a vehicle for rabbit chondrocyte culture. After fourteen days of cell culture, the chondrocyte proliferated greatly and synthesized a large quantity of cartilage matrix in three dimension PGA frame. The PGA chondrocyte complex was prepared and transplanted into a large, full thickness defect in weight bearing surface of the medical femoral condyle. The contralateral knee served as a control. The macroscopic, histologic, electron microscopic evaluations and the thickness of repair tissue measurement were performed postoperatively. Results: There was no immune reaction around the grafts. The ploymer degraded completely in 8 weeks after operation. There was significant difference in the thickness of repair tissue between the grafted ones and the controls ( P <0.01). The typical cartilage tissue was formed and mature chondrocyte was observed under electron microscope 16 weeks after operation. The fibrous tissue was formed in the controls. Conclusion: The full thickness cartilage defects of rabbit has been repaired successfully with method of PGA engineered chondrocytes homotransplantation. It is highly promising for the treatment of articular cartilage defects.
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