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Local Delivery of Autologous Platelet in Collagen Matrix Simulated In Situ Articular Cartilage Repair

机译:胶原基质中自体血小板的局部递送模拟原位关节软骨修复

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Bone marrow released by microfracture or full-thickness cartilage defect can initiate the in situ cartilage repair. However, it can only repair small cartilage defects (<2 cm2). This study aimed to investigate whether autologous platelet-rich plasma (PRP) transplantation in collagen matrix can improve the in situ bone marrow-initiated cartilage repair. Full-thickness cartilage defects (diameter 4 mm, thickness 3 mm) in the patellar grooves of male New Zealand White rabbits were chosen as a model of in situ cartilage repair. They were treated with bilayer collagen scaffold (group II), PRP and bilayer collagen scaffold (group III), and untreated (group I), respectively (n = 11). The rabbits were sacrificed at 6 and 12 weeks after operation. The repaired tissues were processed for histology and for mechanical test. The results showed that at both 6 and 12 weeks, group III had the largest amounts of cartilage tissue, which restored a larger surface area of the cartilage defects. Moreover, group III had higher histological scores and more glycosaminoglycans (GAGs) content than those in the other two groups (p < 0.05). The Young's modulus of the repaired tissue in group II and group III was higher than that of group I (p < 0.05). Autologous PRP and bilayer collagen matrix stimulated the formation of cartilage tissues. The findings implicated that the combination of PRP with collagen matrix may repair larger cartilage defects that currently require complex autologous chondrocyte implantation (ACI) or osteochondral grafting.
机译:微骨折或全层软骨缺损所释放的骨髓可启动原位软骨修复。但是,它只能修复小的软骨缺损(<2 cm2)。本研究旨在探讨胶原基质中自体富血小板血浆(PRP)移植能否改善原位骨髓启动的软骨修复。选择雄性新西兰白兔the骨沟中的全层软骨缺损(直径4 mm,厚度3 mm)作为原位软骨修复的模型。他们分别用双层胶原蛋白支架(第II组),PRP和双层胶原蛋白支架(第III组)治疗,以及未经治疗(第I组)(n = 11)。手术后6和12周处死兔子。修复的组织经过处理以进行组织学检查和力学测试。结果显示,在第6周和第12周,第三组的软骨组织数量最多,从而恢复了较大的软骨缺损表面积。此外,与其他两组相比,第三组具有更高的组织学评分和更多的糖胺聚糖(GAG)含量(p <0.05)。 II组和III组的修复组织的杨氏模量高于I组(p <0.05)。自体PRP和双层胶原基质刺激软骨组织的形成。研究结果表明,PRP与胶原蛋白基质的结合可以修复较大的软骨缺损,而目前这些软骨缺损需要复杂的自体软骨细胞植入(ACI)或骨软骨移植。

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