Biotechnology Unit, Bayer Corporation, Berkeley, CA, USA.
Cytotechnology. 2002 Jan;38(1-3):99-108. doi: 10.1023/A:1021114300958.
A new approach has been developed and used to minimize the timeand more carefully monitor and control the seed-train expansionprocess of recombinant mammalian cell lines. The process uses 50or 100 ml cryo-bags that contain frozen cells at high cell densities of 20 x 10(6) ml(-1) (100 ml bags) or 40 x 10(6) cells ml(-1) (50 ml bags). The frozen bag cell suspension is thawed and transferred directly into a bioreactorthat has been modified such that pH, DO and temperature can becontrolled at the initial volume of two liters (the working volume eventually increases to 12 l). The successful use of thesecryo-bags and the modified ;inoculation' bioreactor to initiate anew seed train expansion of rBHK or rCHO cells is described herein. The interval between cell thawing and the accumulation ofsufficient cell mass to inoculate a production reactor is reducedby at least 25 to 30 days compared to the conventional method that begins with the thaw of 1-2 ml cryo-vials. This ;one-step'technology leads to a much more consistent scale-up by reducingmanual operations and avoiding subjective decisions during the scale-up phase. The cell metabolic rates and product integritywere similar to the control experiments. Furthermore, it was found that it is not necessary to include a wash step to removeDMSO prior to the inoculation.
已经开发并使用了一种新方法,以最小化时间,并更仔细地监测和控制重组哺乳动物细胞系的种子培养扩大过程。该过程使用 50 或 100ml 的冷冻袋,其中包含高细胞密度为 20x10(6)ml(-1)(100ml 袋)或 40x10(6)细胞 ml(-1)(50ml 袋)的冷冻细胞悬浮液。将冷冻袋细胞悬浮液解冻,并直接转移到经过改良的生物反应器中,该生物反应器可以控制 pH、DO 和温度,初始体积为两升(工作体积最终增加到 12 升)。本文描述了这些冷冻袋和改良的“接种”生物反应器在启动新的 rBHK 或 rCHO 细胞种子培养扩大中的成功应用。与传统方法相比,从解冻 1-2ml 冷冻小瓶开始,细胞解冻和积累足够细胞质量以接种生产反应器的时间间隔减少了至少 25-30 天。这种“一步”技术通过减少手动操作并避免在放大阶段做出主观决策,从而实现更一致的放大。细胞代谢率和产物完整性与对照实验相似。此外,还发现接种前不需要进行洗涤步骤以去除 DMSO。