Department of Chemical Engineering and Bioprocess Engineering Research Center, Korea Advanced Institute of Science and Technology, Daeduk Science Town, 305-701, Taejon, Korea.
Cytotechnology. 1995 Oct;17(3):173-83. doi: 10.1007/BF00749655.
A depth filter perfusion system (DFPS) with polypropylene fibers had been demonstrated to support high density cultures of anchorage-independent hybridoma cells. The DFPS provides advantages of high surface-to-volume ratio of 450-600 cm(2)/cm(3), low cost set-up, easy operation and scale-up. To test the feasibility of using DFPS for high density cultures of anchorage-dependent cells, Vero cells were cultivated in the DFPS. Gelatin coating on polypropylene fibers in the DFPS was necessary to promote cell attachment and growth. Dissolved oxygen (DO) concentrations could be controlled by sparging air into the reservoir vessel through a filter sparger. When DO concentration was controlled above 40% of air saturation in the DFPS with 40 μm pore size, the maximum cell concentration as estimated on specific lactate production rate, was 3.81×10(7) cells/ml of the total reactor volume. This viable cell concentration is approximately 18 times higher than that obtained in a T-flask batch culture. Taken together, the results obtained here showed the potential of DFPS for high-density cultures of anchorage-dependent cells.
一种采用聚丙烯纤维的深层过滤灌注系统(DFPS)已被证明可以支持非锚定依赖性杂交瘤细胞的高密度培养。DFPS 具有高比表面积(450-600cm²/cm³)、低成本设置、易于操作和放大等优点。为了测试 DFPS 用于高密度培养锚定依赖性细胞的可行性,将 Vero 细胞在 DFPS 中进行培养。DFPS 中的聚丙烯纤维表面的明胶涂层对于促进细胞附着和生长是必要的。通过在过滤器充气器中向储液瓶中鼓入空气可以控制溶解氧(DO)浓度。当 DO 浓度通过 40μm 孔径的 DFPS 控制在高于空气饱和度的 40%时,根据特定的乳酸盐产生速率估计的最大细胞浓度为 3.81×10(7)个细胞/ml 总反应器体积。这个活细胞浓度比在 T 瓶分批培养中获得的浓度高约 18 倍。综上所述,这些结果表明了 DFPS 用于高密度培养锚定依赖性细胞的潜力。