Itälä A, Nordström E G, Ylänen H, Aro H T, Hupa M
Department of Surgery, University of Turku, FIN-20520 Turku, Finland.
J Biomed Mater Res. 2001 Aug;56(2):282-8. doi: 10.1002/1097-4636(200108)56:2<282::aid-jbm1096>3.0.co;2-5.
Bioactive glasses are surface-active, generally silica-based, synthetic materials that form a firm chemical bond to bone. The aim of this study was to further enhance the bioactivity of glasses by creating a microroughness on their surface. Microroughness increases potential surface area for cell attachment and biomaterial-cell interactions. Three bioactive glasses of different composition were studied. Each material was flame-sprayed into microspheres, and a selected fraction of the spheres (250-300 microm) was sintered to form porous bioactive glass specimens. To create microrough surfaces, different acid etching techniques were tested. Atomic force microscopy (AFM) and back-scattered electron imaging of scanning electron microscopy (BEI-SEM) were used to characterize surface roughness. The degree of roughness was measured by AFM. A novel chemical-etching method, developed through intensive screening of different options, was found consistently to create the desired microroughness, with an average roughness value (R(a)) of 0.35-0.52 microm and a root mean-square roughness value (R(rms)) of 0.42-0.64 microm. Microroughening of the glass surface was obtained even in the internal parts of the porous glass matrices. Measured by BEI-SEM, the etching of a bioactive glass surface did not interfere with the formation of the characteristic surface reactions of bioactive glasses. This was confirmed by immersing the etched and control glass bodies in a simulated body fluid and tris(hydroxymethyl) aminomethane/HCl. The etching process did not significantly affect the mechanical strength of the sintered bioactive glass structures. Based on these experiments, it seems possible to create a reproducible microroughness of appropriate size on the surface of porous bioactive glass. The biologic benefits of such a surface treatment need to be validated with in vivo experiments.
生物活性玻璃是具有表面活性的、通常以二氧化硅为基础的合成材料,它能与骨骼形成牢固的化学键。本研究的目的是通过在玻璃表面制造微粗糙度来进一步提高其生物活性。微粗糙度增加了细胞附着和生物材料 - 细胞相互作用的潜在表面积。研究了三种不同成分的生物活性玻璃。每种材料都通过火焰喷涂制成微球,并将选定部分的微球(250 - 300微米)烧结形成多孔生物活性玻璃标本。为了制造微粗糙表面,测试了不同的酸蚀刻技术。原子力显微镜(AFM)和扫描电子显微镜的背散射电子成像(BEI - SEM)用于表征表面粗糙度。粗糙度程度通过AFM测量。通过对不同选项的深入筛选开发出的一种新型化学蚀刻方法,始终能产生所需的微粗糙度,平均粗糙度值(R(a))为0.35 - 0.52微米,均方根粗糙度值(R(rms))为0.42 - 0.64微米。即使在多孔玻璃基体的内部也能实现玻璃表面的微粗糙化。通过BEI - SEM测量,生物活性玻璃表面的蚀刻并不干扰生物活性玻璃特征性表面反应的形成。将蚀刻后的和对照玻璃体浸入模拟体液和三(羟甲基)氨基甲烷/盐酸中证实了这一点。蚀刻过程并未显著影响烧结生物活性玻璃结构的机械强度。基于这些实验,似乎有可能在多孔生物活性玻璃表面制造出尺寸合适且可重复的微粗糙度。这种表面处理的生物学益处需要通过体内实验来验证。