不同粗化处理对超细晶纯钛表面性能的影响

目的:研究不同粗化处理对超细晶纯钛表面性能及成骨细胞黏附和增殖的影响.方法:将超细晶纯钛棒切割为直径7 mm、厚度2mm的试件,按不同喷砂压力(0.2～0.8 MPa)分组,对其表面进行喷砂酸蚀处理,对照组为普通纯钛.通过表面形貌、粗糙度、亲水性研究材料的表面性能,然后将大鼠胚胎成骨细胞(MC3T3-E1)接种到各组钛片表面,观察细胞初期黏附形态,测定其增殖密度.结果:超细晶纯钛粗化处理后,表面呈现出由喷砂和酸蚀所形成的大小不同的弹坑状双层结构.随着喷砂压力增大,超细晶纯钛表面坑孔直径和粗糙度逐渐增大,但二者均小于普通纯钛对照组(P＜0.05).超细晶纯钛亲水性也随喷砂压力变化而改变,当喷砂压力为0.6 MPa时表现出最佳表面亲水性能.接种细胞后,实验组细胞初期黏附形态优于对照组,当喷砂压力为0.6 MPa时细胞增殖密度最大.结论:对超细晶纯钛喷砂酸蚀处理,喷砂压力为0.6 MPa时,材料表面形貌优于普通纯钛,粗糙度适宜,亲水性良好,更有利于细胞黏附和增殖.

The surface characterization of ultrafine grained titanium after roughness treatment of different types

Objective:To investigate the surface characterization,cell adhension and proliferation of ultrafine grained titanium (UFG Ti) after different sand blasting and acid-etching(SLA).Methods:The billets of UFG Ti and commercially pure titanium Ti(CP Ti) were incised into cylindrical specimens with 7 mm in diameter and 2 mm in height.The specimens were sand blasted at the air pressure of 0.2,0.4,0.6 and 0.8 MPa respectively(n =10) and then acid-etched.The surface morphology,roughness and surface wettability of the specimens were examined.Rat embryo osteoblasts MC3T3-E1 were cultured on the speciments for 1 d,3 d and 5 d respectively,the cell morphology and cell density were observed.Results:The different hierarchical porous topographies were formed on the surface of UFG and CP Ti after modified by SLA.The sizes of blasted holes on the surface and the surface roughness of both materials increased with the increase of blast pressure,but the values of UFG Ti were lower than those of CP Ti correspondingly(P ＜ 0.05).The surface wettability of them was also changed with the blast pressure,but the values of UFG Ti was significantly smaller than those of CP Ti(P ＜ 0.05).When the blast pressure was 0.6 Mpa,the UFG Ti exhibited excellent wettability,the cell density was the highest,the morphology of MC3T3-E1 cells on UFG Ti was superior to that on CP Ti.Conclusion:UFG Ti exhibits proper surface morphology,roughness and excellent wettability,which is more appropriate for adhension and proliferation of MC3T3-E1 cells after modification by SLA at blast pressure of 0.6 Mpa.