搅拌槽生物反应器中单克隆抗体CHO加料批量生产的扩大:流体动力条件和投料方案的影响。

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lucas Lemire, Sebastian-Juan Reyes, Yves Durocher, Robert Voyer, Olivier Henry, Phuong Lan Pham
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引用次数: 0

摘要

为了提高生物反应器的产率,必须仔细选择与水动力学相关的关键参数,如体积功率输入(P/V)、叶轮配置、曝气策略、最大气气量以及适当的进料策略。在本研究中,发现饲喂方式对一种酸盐诱导的CHO投喂批量细胞培养的细胞生长和产量有重要影响。小容量喂养方案避免了渗透压的快速增加,允许延长细胞活力,与大容量喂养方案相比,容量滴度增加33%。雾化空气和氧气都用于溶解氧(DO)控制,利用三个水平的气流速率。最佳气流率为0.0031 vvm,可提高细胞生长、寿命,从而提高最终滴度。更大的空气帽需要更高的气体流速,这导致了更早的细胞死亡。使用恒定的P/V和空气帽体积气体流速(vvm)将生物反应器从1-L放大到10-L,可以获得相当的细胞生长和生产力。通过在整个细胞培养过程中保持P/V和vvm恒定,进一步研究混合和曝气的影响,在诱导后11天进一步提高产品滴度。我们的研究还表明,通过在每次采样事件中去除与饲料添加量相等的培养量来保持恒定的体积,可以显著提高最终的体积滴度。这一发现显示了开发浓缩进料以减少体积增加的好处,这反过来又可以大大减轻扩大规模的任务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scale-up of a monoclonal antibody CHO fed-batch production in stirred tank bioreactors: Effect of hydrodynamic conditions and feeding regimen.

Key hydrodynamic-related parameters such as volumetric power input (P/V), impeller configuration, aeration strategy, and maximum gas sparge rate, as well as an appropriate feeding strategy, must be carefully selected to improve production yields in bioreactor. In this study, the feeding regimen was found to have an important impact on cell growth and productivity of a cumate-inducible CHO fed-batch cell culture. A low-volume feeding regimen avoided a rapid increase in osmolality, allowing for prolonged cell viability and a 33% increase in volumetric titer compared to the high-volume feeding regimen. Both sparged air and oxygen were used for dissolved oxygen (DO) control, utilizing three levels of airflow rates. An optimum airflow rate of 0.0031 vvm was found to improve cell growth, longevity, and thus final titer. A larger air cap required increased gas flow rates, which led to an earlier cell mortality. Scale-up from 1-L to 10-L bioreactor using constant P/V and air cap volumetric gas flow rate (vvm) allowed for comparable cell growth and productivity. Further investigation of the effect of mixing and aeration was done by maintaining P/V and vvm constant throughout the cell culture, which further improved product titers at 11 days after induction. Our study also demonstrates that keeping a constant volume by removing a culture amount equal to the feed volume added at each sampling event can significantly improve the final volumetric titer. This finding shows the benefit of developing a concentrated feed to reduce the volume increase, which in turn could greatly ease the scale-up task.

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来源期刊
Biotechnology Progress
Biotechnology Progress 工程技术-生物工程与应用微生物
CiteScore
6.50
自引率
3.40%
发文量
83
审稿时长
4 months
期刊介绍: Biotechnology Progress , an official, bimonthly publication of the American Institute of Chemical Engineers and its technological community, the Society for Biological Engineering, features peer-reviewed research articles, reviews, and descriptions of emerging techniques for the development and design of new processes, products, and devices for the biotechnology, biopharmaceutical and bioprocess industries. Widespread interest includes application of biological and engineering principles in fields such as applied cellular physiology and metabolic engineering, biocatalysis and bioreactor design, bioseparations and downstream processing, cell culture and tissue engineering, biosensors and process control, bioinformatics and systems biology, biomaterials and artificial organs, stem cell biology and genetics, and plant biology and food science. Manuscripts concerning the design of related processes, products, or devices are also encouraged. Four types of manuscripts are printed in the Journal: Research Papers, Topical or Review Papers, Letters to the Editor, and R & D Notes.
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