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首页> 外文期刊>Key Engineering Materials >Biomimetic Coatings vs. Collagen Sponges as a Carrier for BMP-2: A Comparison of the Osteogenic Responses Triggered in vivo Using an Ectopic Rat Model
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Biomimetic Coatings vs. Collagen Sponges as a Carrier for BMP-2: A Comparison of the Osteogenic Responses Triggered in vivo Using an Ectopic Rat Model

机译:仿生涂料与胶原蛋白海绵作为BMP-2的载体:使用异位大鼠模型在体内触发的成骨反应的比较

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We have developed a new carrier system for bone morphogenetic protein 2 (BMP-2). This agent has been successfully incorporated into biomimetic calcium phosphate implant coatings without losing its osteoinductive potency. Numerous materials have been tested for their efficiency in carrying BMP-2 and in promoting its osteoinductive effects at both ectopic and orthotopic sites. In the present study, we compare the osteoinductive effects of BMP-2 delivered by biomimetic coatings and by classical collagen sponges in vivo using an ectopic rat model. Titanium-alloy discs, either bearing a co-precipitated layer of calcium phosphate and BMP-2 (1.7 μg/disc) or inserted into collagen sponges impregnated with the same drug (10μg/sponge), were implanted subcutaneously in the dorsal region of rats and the bone-formation process monitored after 2 and 5 weeks. After 2 weeks, the net volume of bone formed in the biomimetic coating group (5.8 mm~3/disc) was greater (p < 0.01) than in the collagen sponge one (2.3 mm~3/sponge). By the end of the fifth week, the net volume of bone deposited had increased significantly (p < 0.001) in the biomimetic coating group (11.6 mm~3/disc), whereas in the collagen sponge one it remained unchanged (3.0 mm~3/sponge; p = 0.82). As a carrier for BMP-2 and in facilitating its osteogenic effects, biomimetic calcium phosphate coatings offer a distinct advantage over the classical collagen sponge.
机译:我们已经开发了一种用于骨形态发生蛋白2(BMP-2)的新载体系统。该试剂已成功地掺入仿生磷酸钙植入物涂层中,而不会失去其骨诱导能力。已经测试了许多材料在异位和原位部位携带BMP-2并促进其骨诱导作用的效率。在本研究中,我们使用异位大鼠模型比较了仿生涂层和经典胶原海绵在体内传递的BMP-2的骨诱导作用。将带有磷酸钙和BMP-2共沉淀层(1.7μg/ disc)或插入用相同药物浸渍的胶原海绵(10μg/海绵)中的钛合金椎间盘植入大鼠背侧皮下在2周和5周后监测骨骼形成过程。 2周后,仿生涂层组(5.8 mm〜3 / disc)形成的骨净体积大于胶原海绵1组(2.3 mm〜3 / sponge)(p <0.01)。到第5周结束时,仿生涂层组(11.6 mm〜3 / disc)的骨沉积净体积显着增加(p <0.001),而胶原蛋白海绵组中的净沉积量保持不变(3.0 mm〜3)。 /海绵; p = 0.82)。作为BMP-2的载体并促进其成骨作用,仿生磷酸钙涂层比传统的胶原蛋白海绵具有明显的优势。

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