Ylänen H O, Helminen T, Helminen A, Rantakokko J, Karlsson K H, Aro H T
Department of Chemical Engineering, Abo Akademi University, Turku, Finland.
Ann Chir Gynaecol. 1999;88(3):237-45.
This study was carried out to investigate the use of porous bioactive glass implants in promotion of articular cartilage and subchondral bone repair in large osteochondral joint defects.
Two conical osteochondral defects (top diameter 3.0-3.2 mm) were drilled into the patellar grooves of the distal femurs in the rabbit. The defects, extending (approximately 6-7 mm) from the surface of the articular cartilage to the subchondral marrow space, were reconstructed with size-matched porous conical implants made of sintered bioactive glass microspheres (microsphere diameter 250-300 microm, structural implant compression strength 20-25 MPa) using press-fit technique. The implant surface was smoothened to the level of the surrounding articular cartilage. One of the two defects in each femur was left empty to heal naturally and to serve as the control. At 8 weeks, the defect healing was analyzed with use of a semiquantitative histological grading system, histomorphometry of subchondral bone repair, back-scattered electron imaging of scanning electron microscopy (BEI-SEM), and a microindentation test for characterization for the stiffness properties of the cartilage repair tissue.
The porous structure of the bioactive glass implants, extending from the articular defect of the patellar groove into the posterior cortex of the femur, was extensively filled by new bone. Cartilage repair varied from near-complete healing by hyaline cartilage to incomplete healing predominantly by fibrocartilage or fibrous tissue. There were, however, no statistical differences in the histological scores of repair between the glass-filled and control defects, although the sum of the averages of each category was lowest for the bioactive glass filled defects. The indentation stiffness values of all the defects were also significantly lower than that of normal cartilage on the patellar groove.
Porous textures made by sintering bioactive glass microspheres may expand the opportunities in reconstruction of deep osteochondral defects of weight-bearing joints. The implants act mechanically as a supporting scaffold and facilitate the penetration of stromal bone marrow cells and their chondrogenic and osteogenic differentiation. Ionic properties of the bioactive glasses make the substances highly potential even as delivery systems for adjunct growth factor therapy.
本研究旨在探讨多孔生物活性玻璃植入物在促进大型骨软骨关节缺损处关节软骨和软骨下骨修复中的应用。
在兔股骨远端的髌沟处钻两个圆锥形骨软骨缺损(顶部直径3.0 - 3.2毫米)。缺损从关节软骨表面延伸至软骨下骨髓腔(约6 - 7毫米),使用压配技术,用尺寸匹配的由烧结生物活性玻璃微球制成的多孔圆锥形植入物(微球直径250 - 300微米,结构植入物抗压强度20 - 25兆帕)进行重建。将植入物表面打磨至与周围关节软骨齐平。每只股骨的两个缺损中,一个留空自然愈合作为对照。8周时,使用半定量组织学分级系统、软骨下骨修复的组织形态计量学、扫描电子显微镜背散射电子成像(BEI - SEM)以及用于表征软骨修复组织硬度特性的微压痕试验分析缺损愈合情况。
生物活性玻璃植入物的多孔结构从髌沟的关节缺损延伸至股骨后皮质,被新骨广泛填充。软骨修复情况各异,从透明软骨近乎完全愈合到主要由纤维软骨或纤维组织不完全愈合。然而,尽管生物活性玻璃填充缺损的各分类平均值总和最低,但玻璃填充缺损与对照缺损在修复的组织学评分上无统计学差异。所有缺损的压痕硬度值也显著低于髌沟处正常软骨的硬度值。
烧结生物活性玻璃微球制成的多孔结构可为负重关节深部骨软骨缺损的重建提供更多机会。植入物在机械上起支撑支架作用,促进基质骨髓细胞的穿透及其软骨生成和成骨分化。生物活性玻璃的离子特性使其即使作为辅助生长因子治疗的递送系统也具有很大潜力。