Tabata Y, Miyao M, Yamamoto M, Ikada Y
Institute for Frontier Medical Sciences, Kyoto University, Japan.
J Biomater Sci Polym Ed. 1999;10(9):957-68. doi: 10.1163/156856299x00559.
Vascularization into a poly(vinyl alcohol) (PVA) sponge was investigated using basic fibroblast growth factor (bFGF). This growth factor was impregnated into biodegradable gelatin microspheres for its sustained release and then the bFGF-containing microspheres or free bFGF were incorporated into PVA sponges. Following subcutaneous implantation into the back of mice, the bFGF-containing gelatin microspheres induced vascularization in and around the sponge to a significantly greater extent than that of free bFGF from 3 days after implantation. Significant ingrowth of fibrous tissue into the sponge was also observed when bFGF-containing microspheres were added to the sponge in contrast to free bFGF. Tissue ingrowth occurred into the deeper portion of the sponge over time while it accompanied formation of new capillaries. Empty gelatin microspheres had no effect on vascularization and the level of fibrous tissue ingrowth into the sponge was similar to that of the control group. It was concluded that incorporation of gelatin microspheres containing bFGF into the PVA sponge was effective in prevascularization of the sponge pores.
利用碱性成纤维细胞生长因子(bFGF)研究了聚(乙烯醇)(PVA)海绵的血管化情况。将这种生长因子包埋于可生物降解的明胶微球中以实现其缓释,然后将含bFGF的微球或游离bFGF掺入PVA海绵中。将其皮下植入小鼠背部后,从植入后3天起,含bFGF的明胶微球诱导海绵内部及周围血管化的程度明显高于游离bFGF。与游离bFGF相比,当向海绵中添加含bFGF的微球时,还观察到有大量纤维组织长入海绵。随着时间的推移,组织长入海绵的更深部位,同时伴随着新毛细血管的形成。空明胶微球对血管化没有影响,并且长入海绵的纤维组织水平与对照组相似。得出的结论是,将含bFGF的明胶微球掺入PVA海绵对海绵孔隙的血管预形成有效。