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钕钇铝石榴石激光氮化处理的氮化钛表面对Ti6Al4V基底上MC3T3-E1细胞活性的影响。

Effect of Nd:YAG laser-nitriding-treated titanium nitride surface over Ti6Al4V substrate on the activity of MC3T3-E1 cells.

作者信息

Wang Min, Ning Yingyuan, Zou Haixiao, Chen Si, Bai Yi, Wang Aihua, Xia Haibin

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, Wuhan University, Wuhan, China Department of Oral Implantology, School & Hospital of Stomatology, Wuhan University, Wuhan, China.

出版信息

Biomed Mater Eng. 2014;24(1):643-9. doi: 10.3233/BME-130852.

Abstract

Ti6Al4V discs with a thickness of 2.5 mm and dimensions of 15 × 15 mm2 were fabricated. The titanium nitride (TiN) surface was formed via Nd:YAG laser-nitriding. A sandblast acid-etched (SA) surface was used as a control. Scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), and surface roughness tests were conducted to study the surface and cross-section morphologies as well as the properties of TiN and SA surfaces. MC3T3-E1 osteoblast-like cells were cultured on the TiN and SA surfaces to evaluate the effect of TiN surface on cellular behaviors, including attachment, proliferation and differentiation. Morphological testing results revealed that the cross-section of TiN exhibited dendritic crystallization without cracking. The proliferation and differentiation of MC3T3-E1 cells on the laser-nitriding TiN surface were significantly increased compared to those cultured on SA surface. These findings suggested that the TiN surface generated from Nd:YAG laser-nitriding were favorable for the proliferation and differentiation of MC3T3-E1 cells, which is significant for implant surface modification.

摘要

制备了厚度为2.5 mm、尺寸为15×15 mm2的Ti6Al4V圆盘。通过Nd:YAG激光氮化形成氮化钛(TiN)表面。使用喷砂酸蚀(SA)表面作为对照。进行扫描电子显微镜(SEM)、X射线衍射分析(XRD)和表面粗糙度测试,以研究TiN和SA表面的表面及横截面形态以及性能。将MC3T3-E1成骨样细胞培养在TiN和SA表面上,以评估TiN表面对细胞行为的影响,包括附着、增殖和分化。形态学测试结果显示,TiN的横截面呈现树枝状结晶且无裂纹。与在SA表面培养的细胞相比,MC3T3-E1细胞在激光氮化TiN表面上的增殖和分化显著增加。这些发现表明,Nd:YAG激光氮化产生的TiN表面有利于MC3T3-E1细胞的增殖和分化,这对于植入物表面改性具有重要意义。

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