Department of Biotechnical Production, Dr. Karl Thomae GmbH (Boehringer Ingelheim), Birkendorfer Str. 65, 88397, Biberach/Riss.
Cytotechnology. 1997 Jul;24(2):121-34. doi: 10.1023/A:1007973924865.
Macroporous microcarriers are commonly applied to fixed and fluidized bed bioreactors for the cultivation of stringent adherent cells. Several investigations showed that these carriers are advantageous in respect to a large surface area (Griffiths, 1990; Looby, 1990a).When growing a rC-127 cell line on Cytoline 2 (Pharmacia Biotech), no satisfactory product yield could be achieved. A possible limitation in the supply of nutrient components was investigated to explain these poor results. No significant concentration gradients could be detected. Nevertheless, fluorescence staining revealed a decreasing viability, particularly inside the macroporous structure. Therefore, oxygen transfer to and into the carriers was examined by means of an oxygen microprobe during the entire process. Additional mathematical modeling supported these results.The maximum penetration depth of oxygen was determined to be 300 μm. A critical value influencing the oxygen uptake rate of the rC-127 cells occured at a dissolved oxygen concentration of 8% of air saturation. A significant mass transfer resistance within a laminar boundary film at the surface of the carrier could be detected. This boundary layer had a depth of 170 μm. The results showed that even a 40% air saturation in the bulk liquid could not provide an efficient oxygenation of the surface biofilm during the exponential growth phase. Fluorescent staining reveals a poor viability of cells growing inside the carrier volume. Thus, oxygen supply limits the growth of rC-127 cells on macroporous microcarriers. Poor process performance and low product yield could be explained this way.
大孔微载体常用于固定床和流化床生物反应器中培养严格贴壁的细胞。有几项研究表明,这些载体在大表面积方面具有优势(Griffiths,1990;Looby,1990a)。当在 Cytoline 2(Pharmacia Biotech)上培养 rC-127 细胞系时,无法获得令人满意的产物产量。为了解释这些较差的结果,研究了可能存在的营养成分供应限制。未检测到明显的浓度梯度。然而,荧光染色显示出活力的下降,特别是在大孔结构内部。因此,在整个过程中通过氧微探针检查了向载体中输送和输送氧气的情况。额外的数学模型支持了这些结果。确定了氧气的最大穿透深度为 300μm。在溶解氧浓度为空气饱和度的 8%时,影响 rC-127 细胞耗氧率的临界值发生。在载体表面的层流边界膜内可以检测到明显的传质阻力。该边界层的深度为 170μm。结果表明,即使在主体液体中达到 40%的空气饱和度,也不能在指数生长阶段有效地为表面生物膜供氧。荧光染色显示出细胞在载体内部生长的活力差。因此,氧气供应限制了 rC-127 细胞在大孔微载体上的生长。这种方式可以解释较差的工艺性能和低产物产量。