Graf H, Schügerl K
BASF, Ludwigshafen, Federal Republic of Germany.
Appl Microbiol Biotechnol. 1991 May;35(2):165-75. doi: 10.1007/BF00184681.
Two hybridoma cell lines were cultivated in an indirectly aerated 10-1 reactor in batch, fed-batch and continuous (perfusion) operations and in spinner flasks. The medium in the reactor was sampled either by an aseptic cross-flow filtration module integrated into a loop or by an in-situ tubular filter. The glucose concentration was monitored by an on-line flow injection analyser and the ammonia concentration by an ion-selective electrode. Since the membrane transmission of the high-molecular components decreased during cultivation, the product, a monoclonal antibody, was enriched in the reactor. During cultivation, the concentrations of cells, viable cells, glucose, lactase, acetate, citrate, ammonia, urea, amino acids, proteins, and monoclonal antibodies were determined off-line. The specific growth rate, specific production, and consumption rates of the medium components were influenced considerably by the medium composition, especially by the type and amount of serum used.
两种杂交瘤细胞系在间接通气的10升反应器中进行分批、补料分批和连续(灌注)操作培养,同时也在转瓶中培养。反应器中的培养基通过集成在回路中的无菌错流过滤模块或原位管式过滤器进行采样。葡萄糖浓度通过在线流动注射分析仪监测,氨浓度通过离子选择性电极监测。由于培养过程中高分子成分的膜传输减少,产物单克隆抗体在反应器中得到富集。培养过程中,细胞、活细胞、葡萄糖、乳糖、乙酸盐、柠檬酸盐、氨、尿素、氨基酸、蛋白质和单克隆抗体的浓度通过离线测定。培养基成分的比生长速率、比生产速率和消耗速率受培养基组成的显著影响,尤其是所用血清的类型和量。