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Immunohistochemical Analysis of Osteogenesis Post Magnesium ECAP Miniplate and Screw Implantation using Collagen-1 and Osteocalcin Expression

机译:胶原镁镁型镁镁型Ecap Miniplate的免疫组化分析及胶原蛋白-1和骨质甲酰表达的螺杆植入

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Magnesium is a type of metal with potential as degradable biomaterial. Since it has a high rate of corrosion, ECAP process is done to reduce the rate of degradation and improve its mechanical properties. Nevertheless, biocompatibility is a golden standard of biomaterials and for metals like magnesium relies heavily on corrosion rate. Another necessity for bone implant material is the ability to promote bone formation and accelerate bone healing or fill in bone defects. Due to these reasons, profound understanding on peri-implant osteogenesis and its changes in various period of time becomes very important to be looked into. The purpose of this study is to evaluate osteogenesis after magnesium ECAP miniplate and screw on microscopic preparations of rabbit's femur using immunohistochemical staining on collagen-1 and osteocalcin in 1, 3, and 5 months interval. The results are calculated using semiquantitative method and the decrease of collagen-1 and osteocalcin marker expression indicates bone-implant surface stabilization and neo-osteogenesis improvements. These outcomes lead to the conclusion that measured from biocompatibility indicators, magnesium ECAP can be considered as conventional implant material alternative.
机译:镁是一种金属类型,具有可降解的生物材料。由于它具有很高的腐蚀速率,因此进行了ECAP工艺以降低降解速率并改善其机械性能。然而,生物相容性是生物材料的黄金标准,并且如镁的金属依赖于腐蚀速率。骨植入物质的另一个必要性是促进骨形成和加速骨愈合或填充骨缺损的能力。由于这些原因,对围植入物骨发生的深刻理解及其各种时间段的变化变得非常重要。本研究的目的是评估镁Ecap小型后的骨质发生,并在1,3和5个月间隔内使用免疫组织化学染色兔股骨的微观制剂。使用半定量方法计算结果,并且胶原-1和骨屈曲标记表达的降低表明骨植入表面稳定和新骨质发生改善。这些结果导致了从生物相容性指标中测量的结论,镁ECAP可以被认为是常规植入物质的替代方案。

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