Kokubo Tadashi, Kim Hyun-Min, Kawashita Masakazu
Department of Material Chemistry, Faculty of Engineering, Graduate School of Engineering, Kyoto University, Yoshida, Sakyo-ku, 606-8501, Kyoto, Japan
Biomaterials. 2003 Jun;24(13):2161-75. doi: 10.1016/s0142-9612(03)00044-9.
Some ceramics, such as Bioglass, sintered hydroxyapatite, and glass-ceramic A-W, spontaneously bond to living bone. They are called bioactive materials and are already clinically used as important bone substitutes. However, compared with human cortical bone, they have lower fracture toughness and higher elastic moduli. Therefore, it is desirable to develop bioactive materials with improved mechanical properties. All the bioactive materials mentioned above form a bone-like apatite layer on their surfaces in the living body, and bond to bone through this apatite layer. The formation of bone-like apatite on artificial material is induced by functional groups, such as Si-OH, Ti-OH, Zr-OH, Nb-OH, Ta-OH, -COOH, and PO(4)H(2). These groups have specific structures revealing negatively charge, and induce apatite formation via formations of an amorphous calcium compound, e.g., calcium silicate, calcium titanate, and amorphous calcium phosphate. These fundamental findings provide methods for preparing new bioactive materials with different mechanical properties. Tough bioactive materials can be prepared by the chemical treatment of metals and ceramics that have high fracture toughness, e.g., by the NaOH and heat treatments of titanium metal, titanium alloys, and tantalum metal, and by H(3)PO(4) treatment of tetragonal zirconia. Soft bioactive materials can be synthesized by the sol-gel process, in which the bioactive silica or titania is polymerized with a flexible polymer, such as polydimethylsiloxane or polytetramethyloxide, at the molecular level to form an inorganic-organic nano-hybrid. The biomimetic process has been used to deposit nano-sized bone-like apatite on fine polymer fibers, which were textured into a three-dimensional knit framework. This strategy is expected to ultimately lead to bioactive composites that have a bone-like structure and, hence, bone-like mechanical properties.
一些陶瓷,如生物玻璃、烧结羟基磷灰石和A-W微晶玻璃,能自发地与活骨结合。它们被称为生物活性材料,并且已经在临床上作为重要的骨替代物使用。然而,与人类皮质骨相比,它们的断裂韧性较低,弹性模量较高。因此,开发具有改善机械性能的生物活性材料是很有必要的。上述所有生物活性材料在生物体内其表面都会形成一层类骨磷灰石层,并通过该磷灰石层与骨结合。人工材料上类骨磷灰石的形成是由诸如Si-OH、Ti-OH、Zr-OH、Nb-OH、Ta-OH、-COOH和PO(4)H(2)等官能团诱导的。这些基团具有显示负电荷的特定结构,并通过形成无定形钙化合物,如硅酸钙、钛酸钙和无定形磷酸钙来诱导磷灰石的形成。这些基础研究结果为制备具有不同机械性能的新型生物活性材料提供了方法。可以通过对具有高断裂韧性的金属和陶瓷进行化学处理来制备韧性生物活性材料,例如通过对钛金属、钛合金和钽金属进行NaOH处理和热处理,以及通过对四方氧化锆进行H(3)PO(4)处理。软质生物活性材料可以通过溶胶-凝胶法合成,在该方法中,生物活性二氧化硅或二氧化钛在分子水平上与柔性聚合物,如聚二甲基硅氧烷或聚四甲基氧化物聚合,形成无机-有机纳米杂化物。仿生工艺已被用于在精细的聚合物纤维上沉积纳米级类骨磷灰石,这些纤维被编织成三维针织框架。预计这一策略最终将导致具有类骨结构并因此具有类骨机械性能的生物活性复合材料。