Microfluidic Cell Retention Device for Perfusion of Mammalian Suspension Culture

被引:60
作者
Kwon, Taehong [1 ]
Prentice, Holly [2 ]
De Oliveira, Jonas [3 ]
Madziva, Nyasha [3 ]
Warkiani, Majid Ebrahimi [4 ]
Hamel, Jean-Francois P. [3 ]
Han, Jongyoon [1 ,5 ,6 ]
机构
[1] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
[2] H Prentice Consulting LLC, Carlisle, MA USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] Univ New South Wales, Sch Mech & Mfg Engn, Sydney, NSW, Australia
[5] Singapore MIT Alliance Res & Technol SMART Ctr, BioSyst & Micromech BioSyM IRG, Singapore, Singapore
[6] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
FACTOR-VIII YIELD; ANTIBODY-PRODUCTION; HIGH-DENSITY; ATF; SEPARATION; TFF; MICROFILTRATION; PRODUCTIVITY; FILTRATION; HYBRIDOMA;
D O I
10.1038/s41598-017-06949-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Continuous production of biologics, a growing trend in the biopharmaceutical industry, requires a reliable and efficient cell retention device that also maintains cell viability. Current filtration methods, such as tangential flow filtration using hollow-fiber membranes, suffer from membrane fouling, leading to significant reliability and productivity issues such as low cell viability, product retention, and an increased contamination risk associated with filter replacement. We introduce a novel cell retention device based on inertial sorting for perfusion culture of suspended mammalian cells. The device was characterized in terms of cell retention capacity, biocompatibility, scalability, and long-term reliability. This technology was demonstrated using a high concentration (> 20 million cells/mL) perfusion culture of an IgG(1)-producing Chinese hamster ovary (CHO) cell line for 18-25 days. The device demonstrated reliable and clog-free cell retention, high IgG(1) recovery (> 99%) and cell viability (> 97%). Lab-scale perfusion cultures (350 mL) were used to demonstrate the technology, which can be scaled-out with parallel devices to enable larger scale operation. The new cell retention device is thus ideal for rapid perfusion process development in a biomanufacturing workflow.
引用
收藏
页数:11
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