Wells G D, Fisher M M, Sefton M V
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Ontario, Canada.
Biomaterials. 1993 Jul;14(8):615-20. doi: 10.1016/0142-9612(93)90181-z.
Viable rat hepatocytes were encapsulated in a HEMA-MMA copolymer (80% HEMA). Encapsulated hepatocytes continued to produce urea (a measure of viability) for approximately 2 wk although urea production rates fell steadily over the course of in vitro culture in a pattern similar to those of control hepatocytes in conventional culture. Urea production was slightly higher in 0.01 M Tris buffered glycerol precipitated capsules, relative to phosphate buffered saline precipitated capsules. Hepatocytes were not viable in 0.001 M Tris buffered glycerol precipitated capsules which had a dense wall without the macroporosity seen in the walls of the other capsules. More work is needed to show that HEMA-MMA encapsulated hepatocytes retain some of the differentiated functions of hepatocytes.
将有活力的大鼠肝细胞包封在甲基丙烯酸羟乙酯-甲基丙烯酸甲酯共聚物(80%甲基丙烯酸羟乙酯)中。包封的肝细胞在大约2周内持续产生尿素(活力的一种衡量指标),尽管在体外培养过程中尿素产生速率稳步下降,其模式与传统培养中的对照肝细胞相似。相对于磷酸盐缓冲盐水沉淀的胶囊,在0.01 M Tris缓冲甘油沉淀的胶囊中尿素产生略高。在0.001 M Tris缓冲甘油沉淀的胶囊中肝细胞没有活力,该胶囊壁致密,没有其他胶囊壁中可见的大孔隙。需要更多的研究来表明甲基丙烯酸羟乙酯-甲基丙烯酸甲酯包封的肝细胞保留了肝细胞的一些分化功能。