用CE-MS综合分析仪分析氨胁迫平行微生物反应器平台上生长的中国仓鼠卵巢细胞的废培养基

Kathryn Elliott, Glenn A Harris, S. Harcum, Kenion H. Blakeman, Colin Gavin, Ji Young Anderson
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引用次数: 8

摘要

当致力于生物治疗工艺开发时,在优化生物反应器条件和培养基组成的过程中,对废细胞培养基的分析通常是日常实践。平行微生物反应器系统的引入通过允许同时研究多个生物反应器和培养基变量,降低了工艺开发的复杂性和成本。然而,生物反应器的小体积(通常小于250 mL)限制了可以提取用于每日采样的培养基的体积。我们描述了一种使用集成微芯片毛细管电泳质谱仪(CE-MS)分析仪分析废介质的方法,该分析仪具有最小的样品体积要求和快速的分析时间。该平台使用平行微生物反应器系统(ambr®250)进行评估,该系统培养了受到不同氨(NH3)水平胁迫的中国仓鼠卵巢(CHO)细胞系。废培养基分析确定了所有生物反应器中氨基酸(AA)Ala、Arg、Asp、Glu、Gly、His、Ile、Leu、Lys、Phe、Thr、Trp、Tyr和Val水平的净增加,其中Gly水平在所有生物反应中显示出超过初始水平8倍的增加。其他培养基成分的浓度要么稳定下降,要么在培养结束时完全耗尽。例如,在所有未应激和10mM NH3应激的生物反应器中,Asn都被耗尽,但在培养期结束时,Asn大约是30mM NH3胁迫生物反应器初始水平的两倍。此外,30mM NH3应激条件可能导致胆碱的完全降解或快速消耗,因为从t=36小时采样开始,胆碱不再存在。总体而言,根据细胞的喂养和消耗,并根据应激条件,观察到受监测的培养基成分具有独立的轨迹。更频繁地进行废介质分析的能力将允许实时观察这些过程变化和相关的控制策略。用CE-MS综合分析仪分析氨胁迫平行微生物反应器平台上生长的中国仓鼠卵巢细胞的废培养基
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spent Media Analysis with an Integrated CE-MS Analyzer of Chinese Hamster Ovary Cells Grown in an Ammonia-Stressed Parallel Microbioreactor Platform
W hen working on biotherapeutic process development, the analysis of spent cell culture media is often a daily practice during the optimization of bioreactor conditions and media composition. The introduction of parallel microbioreactor systems has decreased the complexity and costs of process development by allowing for concurrent studies of multiple bioreactor and media variables. However, the bioreactors’ small volumes (typically less than 250 mL) limit the volume of media one can extract for daily sampling. We describe a means to analyze spent media with an integrated microchip capillary electrophoresis mass spectrometer (CE-MS) analyzer with minimal sample volume requirements and rapid analysis time. The platform was evaluated with a parallel microbioreactor system (ambr® 250) culturing a Chinese hamster ovary (CHO) cell line stressed by varying levels of ammonia (NH3). The spent media analysis identified net increases in the levels of the amino acids (AA) Ala, Arg, Asp, Glu, Gly, His, Ile, Leu, Lys, Phe, Thr, Trp, Tyr, and Val in all bioreactors, with Gly levels showing increases in excess of 8-fold initial levels in all bioreactors. Other media components either steadily decreased in concentration or were completely depleted by the end of culture. For example, Asn was depleted in all of the unstressed and 10 mM NH3-stressed bioreactors, but was approximately twice as high as the initial levels in the 30 mM NH3-stressed bioreactors at the end of the culture periods. Also, the 30 mM NH3-stressed condition may have caused either complete degradation or rapid consumption of choline, since it was no longer present starting at the t = 36 h sampling. Overall, the monitored media components were observed to have independent trajectories based on feeding and consumption by the cells, and depending on the stressed condition. The capability to have more frequent spent media analyses would allow for real-time observation of these process changes and associated control strategies. Spent Media Analysis with an Integrated CE-MS Analyzer of Chinese Hamster Ovary Cells Grown in an Ammonia-Stressed Parallel Microbioreactor Platform
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