Ju Young Min, Park Kwideok, Son Jun Sik, Kim Jae-Jin, Rhie Jong-Won, Han Dong Keun
Biomaterials Research Center, Korea Institute of Science and Technology, P.O. Box 131, Cheongryang, Seoul 130-650, Korea.
J Biomed Mater Res B Appl Biomater. 2008 Apr;85(1):252-60. doi: 10.1002/jbm.b.30943.
Three dimensional (3D) porous poly(L-lactic acid) (PLLA) scaffolds were fabricated using a modified gas foaming method whose effervescent porogens were a mixture of sodium bicarbonate and citric acid. To improve chondrocyte adhesion, the scaffolds were then hydrophilized through oxygen plasma treatment and in situ graft polymerization of acrylic acid (AA). When the physical properties of AA-grafted scaffolds were examined, the porosity and pore size were 87 approximately 93% and 100 approximately 300 microm, respectively. The pore sizes were highly dependent on the varying ratios (w/w) between porogen and polymer solution. Influenced by their pore sizes, the compressive moduli of scaffolds significantly decreased with increasing pore size. The altered surface characteristics were clearly reflected in the reduced water contact angles that meant a significant hydrophilization with the modified polymer surface. Electron spectroscopy for chemical analysis (ESCA) and time-of-flight secondary ion mass spectrometer (ToF-SIMS) also confirmed the altered surface chemistry. When chondrocytes were seeded onto the AA-grafted PLLA scaffolds, cell adhesion and proliferation were substantially improved as compared to the unmodified scaffolds. The benefit of the modified scaffolds was clear in the gene expressions of collagen type II that was significantly upregulated after 4-week culture. Safranin-O staining also identified greater glycosaminoglycan (GAG) deposition in the modified scaffold. The AA-grafted porous polymer scaffolds were effective for cell adhesion and differentiation, making them a suitable platform for tissue-engineered cartilage.
采用改良气体发泡法制备了三维(3D)多孔聚(L-乳酸)(PLLA)支架,其泡腾致孔剂为碳酸氢钠和柠檬酸的混合物。为了提高软骨细胞的黏附性,随后通过氧等离子体处理和丙烯酸(AA)的原位接枝聚合对支架进行了亲水化处理。在检测AA接枝支架的物理性能时,孔隙率和孔径分别约为87%至93%和100至300微米。孔径高度依赖于致孔剂与聚合物溶液之间不同的比例(w/w)。受孔径影响,支架的压缩模量随孔径增加而显著降低。改变的表面特性明显反映在水接触角的减小上,这意味着改性聚合物表面具有显著的亲水化。化学分析电子能谱(ESCA)和飞行时间二次离子质谱仪(ToF-SIMS)也证实了表面化学的改变。当将软骨细胞接种到AA接枝的PLLA支架上时,与未改性的支架相比,细胞黏附和增殖得到了显著改善。在4周培养后,II型胶原蛋白的基因表达显著上调,这清楚地表明了改性支架的优势。番红O染色也显示改性支架中有更多的糖胺聚糖(GAG)沉积。AA接枝的多孔聚合物支架对细胞黏附和分化有效,使其成为组织工程软骨的合适平台。