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首页> 外文期刊>Journal of orthopaedic research >Transplantation of cryopreserved osteochondral Dowel allografts for repair of focal articular defects in an ovine model.
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Transplantation of cryopreserved osteochondral Dowel allografts for repair of focal articular defects in an ovine model.

机译:冷冻保存的骨软骨钉钉同种异体移植修复绵羊模型中的局灶性关节缺损。

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The purpose of this study was to test whether successful cryopreservation of osteochondral tissue is possible and whether, with the appropriate surgical procedure, it can be used for the successful repair of focal articular defects within joints. Fresh (nonfrozen) and snap-frozen (plunged in liquid nitrogen and thawed in a water bath at 37 degrees C, repeated three times) autografts were used as positive and negative controls, respectively. Snap-frozen, frozen (fresh tissue placed in a freezer at -80 degrees C), and cryopreserved (immersed in 10% dimethyl sulfoxide for 30 minutes and then frozen at 1 degrees C/min to -80 degrees C) allografts were transplanted into the knees of adult sheep. Outcomes were evaluated 3, 6, and 12 months after transplantation. The morphological, histological, biochemical, and biomechanical behaviors and characteristics of the graft cartilage, the host cartilage adjacent to the grafts, and the opposing tibial cartilage were assessed. Freezing protocols that yielded poor chondrocyte recovery after thawing (frozen and snap-frozen) resulted in poor overall graft outcome. The cryopreservation protocol, however, resulted in intermediate recovery (50%) of chondrocytes and in intermediate overall graft outcome compared with fresh autografts. The membrane integrity of the allograft chondrocytes immediately following cryopreservation was identified as the most reliable predictor of long-term outcome of the graft. Further improvements in cryopreservation technique may lead to an effective method of banking osteochondral tissue for successful transplantation for the repair of focal defects and larger joint reconstructions.
机译:这项研究的目的是测试是否可以成功冷冻保存骨软骨组织,以及是否可以通过适当的手术程序将其成功用于修复关节内局灶性关节缺损。新鲜的(未冷冻的)和速冻的(浸入液氮中,并在37摄氏度的水浴中融化,重复3次)分别用作阳性和阴性对照。将速冻,冷冻(将新鲜组织放入-80摄氏度的冰箱中)和冷冻保存(浸入10%二甲基亚砜中30分钟,然后以1摄氏度/分钟的速度冷冻至-80摄氏度)的同种异体移植物成年绵羊的膝盖。在移植后3、6和12个月评估结果。评估了移植软骨,与移植物相邻的宿主软骨以及相对的胫骨软骨的形态,组织学,生化和生物力学行为和特征。解冻(冷冻和速冻)后导致软骨细胞恢复不良的冷冻方案导致整体移植物效果不佳。然而,与新鲜的自体移植相比,冷冻保存方案可导致软骨细胞的中期恢复(50%)和整体移植的中期结果。冷冻保存后,同种异体移植软骨细胞的膜完整性被认为是移植物长期结果的最可靠预测指标。冷冻保存技术的进一步改进可能会导致一种有效的方法使骨软骨组织堆积以成功移植,以修复局灶性缺损和更大的关节重建。

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