Dynamics of single cell property distributions in Chinese hamster ovary cell cultures monitored and controlled with automated flow cytometry

被引:24
|
作者
Kacmar, J
Srienc, F
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Biotechnol Inst, Gortner Lab 240, St Paul, MN 55108 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
automated flow cytometry; bioreactor controls; bioreactor monitoring; cytostat; mammalian cell culture; single cell heterogeneity;
D O I
10.1016/j.jbiotec.2005.06.031
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Two important variables that are often not measured online in Chinese hamster ovary (CHO) cell cultures are cell number concentration and culture viability. We have developed an automated flow cytometry system that measured the cell number concentration, single cell viability based on propidium iodide (PI) exclusion, and single cell light scattering from bioreactor samples every 30 min. The bioreactor was monitored during batch growth, and then the cell number concentration was controlled at a set point during cytostat operation. NH4Cl was added during steady state operation in cytostat mode to monitor the transient cell population response to adverse growth conditions. The automated measurements correlated well to cell concentration and viability determined manually using a hemacytometer. The described system provides a method to study mammalian cell culture physiology and dynamics in great detail. It presents a new method for the monitoring and control of animal cell culture. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:410 / 420
页数:11
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