首页> 美国卫生研究院文献>Journal of Cellular and Molecular Medicine >Asprin‐loaded strontium‐containing α‐calcium sulphate hemihydrateano‐hydroxyapatite composite promotes regeneration of critical bone defects
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Asprin‐loaded strontium‐containing α‐calcium sulphate hemihydrateano‐hydroxyapatite composite promotes regeneration of critical bone defects

机译:含叶蛋白含锶的α-硫酸钙半水合物/纳米 - 羟基磷灰石复合材料促进了临界骨缺损的再生

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摘要

Our laboratory originally synthesized strontium(Sr)‐containing α‐calcium sulphate hemihydrateano‐hydroxyapatite composite (Sr‐α‐CSH‐HA) and demonstrated its ability to repair critical bone defects. This study attempted to incorporate aspirin into it to produce a better bone graft material for critical bone defects. After 5% Sr‐α‐CSH was prepared by coprecipitation and hydrothermal methods, it was mixed with aspirin solution of different concentrations (50 μg/ml, 200 μg/ml, 800 μg/ml and 3200 μg/ml) at a fixed liquid‐solid ratio (0.54 v/w) to obtain aspirin‐loaded Sr‐α‐CSH‐HA composite. In vitro experiments were performed on the composite extracts. The tibial defects (3 mm*5 mm) in SD rat model were filled with the composite for 4 weeks and 12 weeks to evaluate its osteogenic capacity in vivo. Our results showed its capability of proliferation, migration and osteogenesis of BMSCs in vitro got improved. In vivo treatment with 800 μg/ml aspirin–loaded Sr‐α‐CSH‐HA composite led to significantly more new bone formation in the defects compared with Sr‐α‐CSH‐HA composite and significantly promoted the expression of osteogenic‐related genes and inhibited osteoclast activity. In general, our research suggests that aspirin‐loaded Sr‐α‐CSH‐HA composite may have a greater capacity of repairing tibial defects in SD rats than simple Sr‐α‐CSH‐HA composite.
机译:我们的实验室最初合成锶(SR) - α-硫酸钙半水合物/纳米羟基磷灰石复合物(SR-α-CSH / N-HA),并证明了其修复临界骨缺陷的能力。该研究试图将阿司匹林掺入其中以生产用于临界骨缺陷的更好的骨移植材料。在通过共沉淀和水热方法制备5%SR-α-CSH后,将其在固定液体下与不同浓度(50μg/ ml,200μg/ ml,800μg/ ml和3200μg/ ml的阿司匹林溶液混合 - 溶血率(0.54V / W),得到阿司匹林负载的SR-α-CSH / N-HA复合材料。在复合提取物上进行体外实验。 SD大鼠模型中的胫骨缺陷(3mm * 5mm)填充了复合材料4周和12周,以评估其体内的骨质发生能力。我们的结果表明,体外BMSCs的增殖,迁移和骨质发生能力得到改善。在体内处理用800μg/ ml加载的SR-α-CSH / N-HA复合材料导致缺陷的骨形成明显更新,与SR-α-CSH / N-HA复合有显着促进了成骨的表达 - 相关的基因和抑制骨质糖活性。一般来说,我们的研究表明阿司匹林负载的SR-α-CSH / N-HA复合物在SD大鼠中可以具有比简单的SR-α-CSH / N-HA复合材料在SD大鼠中修复胫骨缺陷的能力更大。

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