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ECTOPIC OSTEOINDUCTION BY VARIOUSLY DEMINERALIZED ALLOGENIC CORTICAL BONE MATRIX

机译:不同半异质同质骨基质的异位骨诱导

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摘要

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 ℃ 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 ℃ 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 ℃ is a rapid and effective method for sterile demineralized graft preparation.
机译:为了提高去矿质骨基质的成骨愈合效率,我们评估了大鼠皮下和肌肉部位各种去矿质异体皮质骨基质诱导的异位骨形成。将大鼠肾小管皮质骨基质在60℃加热的0.6N HCl中分别用控温超声清洁剂脱盐5分钟和20分钟,然后在大鼠背侧皮下袋和大腿肌肉中植入1-3周。还通过MTT测定和ALP染色在体外评估了骨基质的脱矿质条件对细胞增殖和成骨分化的影响。通过超声处理和加热稀释的0.6 N HCl,在20分钟内将皮质基质完全脱盐。在60℃的酸性溶液中超声处理的骨基质在体内均无不良的免疫原性和炎症反应,无论脱盐条件如何。更充分的脱矿质有助于细胞增殖和成骨细胞分化。异位骨形成仅由去矿质骨基质诱导,在完全去矿质基质中更有利。皮下囊比肌组织更有利于异位骨诱导。这些发现表明,完全脱矿质的皮质骨基质可以通过暴露更多的生物活性分子来最大化成骨修复,这些分子又可以诱导植入基质周围间充质细胞的软骨分化和成骨分化,并且在60℃加热的0.6 N HCl稀释液的超声处理是一种快速有效的无菌脱矿质移植物制备方法。

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