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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >In vitro degradability, bioactivity and cell responses to mesoporous magnesium silicate for the induction of bone regeneration
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In vitro degradability, bioactivity and cell responses to mesoporous magnesium silicate for the induction of bone regeneration

机译:对介孔硅酸镁的体外降解性,生物活性和细胞反应,以诱导骨再生

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摘要

Mesoporous magnesium silicate (m-MS) was synthesized, and the in vitro degradability, bioactivity and primary cell responses to m-MS were investigated. The results suggested that the m-MS with mesoporous channels of approximately 5 nm possessed the high specific surface area of 451.0 m(2)/g and a large specific pore volume of 0.41 cm(3)/g compared with magnesium silicate (MS) without mesopores of 75 m2/g and 0.21 cm(3)/g, respectively. The m-MS was able to absorb a large number of water, with water absorption of 74% compared with 26% for MS. The m-MS was also degradable in a Tris-HCI solution, with a weight loss ratio of 40 wt% after a 70-day immersion period. The m-MS exhibited good in vitro bioactivity, inducing apatite formation on its surfaces after soaking in simulated body fluid (SBF) at a faster rate than observed for MS. The m-MS surface clearly promoted the proliferation and differentiation of MC3T3-E1 cells, and their normal cell morphology indicated excellent cytocompatibility. This study suggested that mesoporous magnesium silicate with a high specific surface area and pore volume had suitable degradability and good bioactivity and biocompatibility, making it an excellent candidate biomaterial for the induction of bone regeneration. (C) 2014 Elsevier B.V. All rights reserved.
机译:合成了介孔硅酸镁(m-MS),并研究了其对m-MS的体外降解性,生物活性和原代细胞反应。结果表明,与硅酸镁(MS)相比,具有约5 nm介孔通道的m-MS具有451.0 m(2)/ g的高比表面积和0.41 cm(3)/ g的大比孔体积没有中孔分别为75 m2 / g和0.21 cm(3)/ g。 m-MS能够吸收大量水,吸水率为74%,而MS为26%。 m-MS在Tris-HCl溶液中也可降解,浸入70天后的重量损失率为40 wt%。 m-MS表现出良好的体外生物活性,以比MS观察到的更快的速度浸入模拟体液(SBF)后诱导其表面形成磷灰石。 m-MS表面明显促进了MC3T3-E1细胞的增殖和分化,并且它们的正常细胞形态显示出极好的细胞相容性。这项研究表明,具有高比表面积和孔体积的中孔硅酸镁具有合适的降解性,良好的生物活性和生物相容性,使其成为诱导骨再生的极佳候选生物材料。 (C)2014 Elsevier B.V.保留所有权利。

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