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Critical Role of Silicon in Directing the Bio-inspired Mineralization of Gelatin in the Presence of Hydroxyapatite
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作者 Ruijuan Yao Yao Wang +7 位作者 Bo zhang Juan Liu nihui zhang Jing He Guolong Meng Bo Jiang Shanling Wang Fang Wu 《Journal of Bionic Engineering》 SCIE EI CSCD 2021年第6期1413-1429,共17页
Significant progress has been made on understanding the critical role of organic components in directing the collagen mineralization.We hypothesize that the inorganic trace elements might also play important role in t... Significant progress has been made on understanding the critical role of organic components in directing the collagen mineralization.We hypothesize that the inorganic trace elements might also play important role in the mineralization of collagenous matrix.To this aim,we systematically compared the in-vitro biomineralization behaviors of gelatin,gelatin-HA and gelatin-SiHA electrospun membranes.The results indicated that the presence of Si ions played a striking influence on the nucleation behaviors and mineralized structures.The gelatin-SiHA samples demonstrated more homogeneous nucleation within the gelatin fiber and growth along the fiber direction,in comparison with the heterogeneous nucleation and growth of spherulitic clusters on top of the nanofiber surface,i.e.extrafibrillar mineralization.The likely shift of the nucleation mode to the intrafibrillar mineralization in the presence of Si ions led to good alignment of apatite c-axis with the long axis of the nanofiber,resulting in a mineralization process and microstructure that were closer to those in natural bone.Cellular response analysis indicated that Si incorporation improved the MSC attachment and cytoskeleton organization.Such findings might have important implication in both understanding the complex mechanisms involved in collagen mineralization and optimal designing of advanced bio-inspired materials with potential superior mechanical and biological properties. 展开更多
关键词 SILICON HYDROXYAPATITE BIOMINERALIZATION Electrospinning NANOFIBER GELATIN
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