Non-invasive real-time monitoring of cell concentration and viability using Doppler ultrasound

被引:4
作者
Akbari, Samin [1 ]
Anderson, Phillip [2 ]
Zang, Han [3 ]
Ganjian, Amin [4 ]
Balke, Robert [5 ]
Kwon, Taehong [1 ]
Pollard, David [1 ]
机构
[1] Sartorius Stedim North Amer Inc, Bohemia, NY 11716 USA
[2] Andersonics LLC, Belmont, MA USA
[3] Boston Univ, Boston, MA USA
[4] Sartorius Canada Inc, Oakville, ON, Canada
[5] EE Partners LLC, Winchester, MA USA
来源
SLAS TECHNOLOGY | 2022年 / 27卷 / 06期
关键词
Process analytics tools (PAT); Doppler ultrasound; Bioprocessing; Cell viability; Cell concentration; Multivariate data analysis (MVDA); RAMAN-SPECTROSCOPY; CULTURE; DENSITY;
D O I
10.1016/j.slast.2022.09.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bioprocess optimization towards higher productivity and better quality control relies on real-time process mon-itoring tools to measure process and culture parameters. Cell concentration and viability are among the most important parameters to be monitored during bioreactor operations that are typically determined using optical methods on an extracted sample. In this paper, we have developed an online non-invasive sensor to measure cell concentration and viability based on Doppler ultrasound. An ultrasound transducer is mounted outside the biore-actor vessel and emits a high frequency tone burst (15 MHz) through the vessel wall. Acoustic backscatter from cells in the bioreactor depends on cell concentration and viability. The backscattered signal is collected through the same transducer and analyzed using multivariate data analysis (MVDA) to characterize and predict the cell culture properties. We have developed accurate MVDA models to predict the Chinese hamster ovary (CHO) cell concentration in a broad range from 0.1 x 10 6 cells/mL to 100 x 10 6 cells/mL, and cell viability from 3% to 99%. The non-invasive monitoring is ideal for single use bioreactor and the in-situ measurements removes the burden for offline sampling and dilution steps. This method can be similarly applied to other suspension cell culture modalities.
引用
收藏
页码:368 / 375
页数:8
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