Sosnowski Stanislaw, Woźniak Piotr, Lewandowska-Szumieł Małgorzata
Center of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland.
Macromol Biosci. 2006 Jun 16;6(6):425-34. doi: 10.1002/mabi.200600003.
This paper presents a method for the preparation of porous poly(L-lactide)/poly[(L-lactide)-co-glycolide] scaffolds for tissue engineering. Scaffolds were prepared by a mold pressing-salt leaching technique from structured microparticles. The total porosity was in the range 70-85%. The pore size distribution was bimodal. Large pores, susceptible for osteoblasts growth and proliferation had the dimensions 50-400 microm. Small pores, dedicated to the diffusion of nutrients or/and metabolites of bone forming cells, as well as the products of hydrolysis of polyesters from the walls of the scaffold, had sizes in the range 2 nm-5 microm. The scaffolds had good mechanical strength (compressive modulus equal to 41 MPa and a strength of 1.64 MPa for 74% porosity). Scaffolds were tested in vitro with human osteoblast-like cells (MG-63). It was found that the viability of cells seeded within the scaffolds obtained using the mold pressing-salt leaching technique from structured microparticles was better when compared to cells cultured in scaffolds obtained by traditional methods. After 34 d of culture, cells within the tested scaffolds were organized in a tissue-like structure. Photos of section of macro- and mesoporous PLLA/PLGA scaffold containing 50 wt.-% of PLGA microspheres after 34 d of culture. Dark spots mark MG-63 cells, white areas belong to the scaffold. The specimen was stained with haematoxylin/eosin. Bar = 100 microm.
本文介绍了一种用于组织工程的多孔聚(L-丙交酯)/聚(L-丙交酯-共-乙交酯)支架的制备方法。支架通过模压-盐沥滤技术由结构化微粒制备而成。总孔隙率在70%-85%范围内。孔径分布呈双峰态。有利于成骨细胞生长和增殖的大孔尺寸为50-400微米。小孔隙用于营养物质或/和成骨细胞代谢产物的扩散,以及支架壁上聚酯水解产物的扩散,其尺寸范围为2纳米-5微米。支架具有良好的机械强度(对于孔隙率为74%的支架,压缩模量等于41兆帕,强度为1.64兆帕)。使用模压-盐沥滤技术从结构化微粒获得的支架在体外用人成骨样细胞(MG-63)进行了测试。结果发现,与在传统方法制备的支架中培养的细胞相比,在使用模压-盐沥滤技术从结构化微粒获得的支架中接种的细胞活力更好。培养34天后,测试支架内的细胞组织成类似组织的结构。培养34天后含50重量%-PLGA微球的大孔和中孔PLLA/PLGA支架切片的照片。黑点标记MG-63细胞,白色区域属于支架。标本用苏木精/伊红染色。标尺=100微米。