Brekke J H, Toth J M
THM Biomedical, Inc., Duluth, Minnesota 55802, USA.
J Biomed Mater Res. 1998 Winter;43(4):380-98. doi: 10.1002/(sici)1097-4636(199824)43:4<380::aid-jbm6>3.0.co;2-d.
This article presents a strategy for design, engineering, and fabrication of a bioresorbable, manufactured bone graft substitute (BGS) device. The approach is based on established precepts of osteogenesis, molecular biology of hyaluronic acid and osteoinductive proteins, and theoretical preformance criteria for such a device collated from the literature of 1991 to 1996. Application of this design and engineering strategy results in a composite device consisting of a D,D-L,L-polylactic acid macrostructure optimized to the architecture of cancellous bone, a microstructure composed of a filamentous velour of hyaluronan and a recombinant human bone morphogenetic protein 2 (rhBMP-2). The performance of this construct was tested in vivo in the dog, intertransverse process, spinal fusion model and in a critical sized defect of the rabbit radius. Data from these studies are used to illustrate principle points of the design and engineering concept.
本文介绍了一种用于设计、制造可生物吸收的人工骨移植替代物(BGS)装置的策略。该方法基于已确立的骨生成原则、透明质酸和骨诱导蛋白的分子生物学,以及从1991年至1996年的文献中整理出的此类装置的理论性能标准。应用这种设计和工程策略可得到一种复合装置,它由优化为松质骨结构的D,D-L,L-聚乳酸宏观结构、由丝状透明质酸绒和重组人骨形态发生蛋白2(rhBMP-2)组成的微观结构构成。在犬的横突间脊柱融合模型以及兔桡骨临界尺寸缺损模型中对该构建体进行了体内性能测试。这些研究的数据用于阐明设计和工程概念的要点。