首页> 外文会议>Asian Symposium on biomedical materials >ECT0P1C OSTEOINDUCTION BY VARIOUSLY DEMINERALIZED ALLOGENIC CORTICAL BONE MATRIX
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ECT0P1C OSTEOINDUCTION BY VARIOUSLY DEMINERALIZED ALLOGENIC CORTICAL BONE MATRIX

机译:Ect0p1c骨液通过各种脱矿化的同种异体皮质骨基质

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To improve ostegenic healing efficiency by demineralized bone matrix, we evaluated the ectopic bone formation induced by variously demineralized allogenic cortical bone matrices at subcutaneous and muscular sites in rats. The rat tubular cortical bone matrices were demineralized in heated 0.6N HCl at 60 deg C for 5 and 20 mins, respectively, using a controlled-heat ultrasonic cleaner and implanted in rat dorsal subcutaneous pouches and thigh muscles for 1-3 weeks. The influence of the demineralized condition of bone matrix on cellular proliferation and osteogenic differentiation was also evaluated in vitro by MTT assay and ALP staining. The cortical matrices were completely demineralized within 20 mins by sonication and heating of diluted 0.6 N HCl. The sonicated bone matrices in heated acidic solution at 60 deg C revealed no adverse immunogenic and inflammatory response in vivo regardless of demineralized condition. Cellular proliferation and osteoblastic differentiation was facilitated by more fully demineralized. Ectopic bone formation was induced only by demineralized bone matrices and were more favorable in fully demineralized matrices. The ectopic bone induction was more favorably in subcutaneous pouches than in muscular tissue. These findings suggest that a fully demineralized cortical bone matrix maximizes osteogenic repair by exposing more bioactive molecules which in turn induce chondro- and osteognic differentiation of mesenchymal cells around the implanted matrices, and that the sonication of diluted 0.6 N HCl heated at 60 deg C is a rapid and effective method for sterile demineralized graft preparation.
机译:为了通过脱矿质骨基质提高骨质愈合效率,我们评估了在大鼠皮下和肌肉点的各种脱矿的同种异体皮质骨基质诱导的异位骨形成。使用受控热超声波清洁剂分别在60℃下,在60℃下,在60℃下,在60℃下,在60℃下,在60℃和20分钟,并植入大鼠背部皮下袋和大腿肌肉1-3周,将大鼠管状皮质骨质基质脱落。通过MTT测定和ALP染色,还评估了骨基质骨基质的脱落条件对细胞增殖和骨质发生分化的影响。通过超声处理和加热稀释0.6nHcl,皮质基质在20分钟内完全脱矿质。在60℃下加热酸性溶液中的超声骨基质显示出在vivo中没有不良免疫原性和炎症反应,而不管脱矿质状况。通过更全面的脱矿质促进细胞增殖和骨细胞分化。仅通过脱矿质骨基质诱导异位骨形成,并且在完全脱矿质基质中更有利。在皮下袋中的异位骨诱导比在肌肉组织中更有利。这些发现表明,全矿化的皮质骨基质通过暴露更多的生物活性分子,最大化成骨修复,这反过来归因于植入基质周围的间充质细胞的软骨和骨骨细胞分化,并且在60℃下加热的稀释0.6nHCl的超声处理是一种快速有效的无菌脱蛋白接枝制剂方法。

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