Davies John E
Institute of Biomaterials and Biomedical Engineering, University of Toronto, 164 College Street, Toronto, Ontario, Canada M5S 3G9.
Biomaterials. 2007 Dec;28(34):5058-67. doi: 10.1016/j.biomaterials.2007.07.049. Epub 2007 Aug 13.
Bone bonding is occurring in each of us and all other terrestrial vertebrates throughout life at bony remodeling sites. The surface created by the bone-resorbing osteoclast provides a three-dimensionally complex surface with which the cement line, the first matrix elaborated during de novo bone formation, interdigitates and is interlocked. The structure and composition of this interfacial bony matrix has been conserved during evolution across species; and we have known for over a decade that this interfacial matrix can be recapitulated at a biomaterial surface implanted in bone, given appropriate healing conditions. No evidence has emerged to suggest that bone bonding to artificial materials is any different from this natural biological process. Given this understanding it is now possible to explain why bone-bonding biomaterials are not restricted to the calcium-phosphate-based bioactive materials as was once thought. Indeed, in the absence of surface porosity, calcium phosphate biomaterials are not bone bonding. On the contrary, non-bonding materials can be rendered bone bonding by modifying their surface topography. This paper argues that the driving force for bone bonding is bone formation by contact osteogenesis, but that this has to occur on a sufficiently stable recipient surface which has micron-scale surface topography with undercuts in the sub-micron scale-range.
在我们每个人以及所有其他陆生脊椎动物的一生中,骨结合在骨重塑部位都会发生。破骨细胞吸收骨组织所形成的表面是一个三维复杂表面,新生骨形成过程中首先形成的基质——黏合线与之相互交错并锁合。这种界面骨基质的结构和组成在物种进化过程中一直得以保留;而且十多年来我们就知道,在适当的愈合条件下,植入骨内的生物材料表面能够重现这种界面基质。目前尚无证据表明骨与人工材料的结合与这种自然生物学过程有任何不同。基于这种认识,现在就可以解释为什么骨结合生物材料并不局限于曾经认为的基于磷酸钙的生物活性材料。事实上,在没有表面孔隙的情况下,磷酸钙生物材料并不具备骨结合能力。相反,通过改变非结合材料的表面形貌,可以使其具备骨结合能力。本文认为,骨结合的驱动力是接触性骨生成导致的骨形成,但这必须发生在足够稳定的受体表面,该表面具有微米级的表面形貌且在亚微米尺度范围内有底切。