Design and development of a new ambr250® bioreactor vessel for improved cell and gene therapy applications

被引:31
作者
Rotondi, Marco [1 ]
Grace, Ned [2 ]
Betts, John [2 ]
Bargh, Neil [2 ]
Costariol, Elena [1 ]
Zoro, Barney [2 ]
Hewitt, Christopher J. [3 ]
Nienow, Alvin W. [3 ,4 ]
Rafiq, Qasim A. [1 ]
机构
[1] UCL, Adv Ctr Biochem Engn, Dept Biochem Engn, Gower St, London WC1E 6BT, England
[2] Sartorius Stedim Biotech, York Way, Royston SG8 5WY, England
[3] Aston Univ, Sch Life & Hlth Sci, Aston Med Res Inst, Birmingham B4 7ET, W Midlands, England
[4] Univ Birmingham, Sch Chem Engn, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会; “创新英国”项目;
关键词
Ambr250; Bioreactor; Vessel; Bioprocessing; Automation; hMSC; T-cell;
D O I
10.1007/s10529-021-03076-3
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
The emergence of cell and gene therapies has generated significant interest in their clinical and commercial potential. However, these therapies are prohibitively expensive to manufacture and can require extensive time for development due to our limited process knowledge and understanding. The automated ambr250 (R) stirred-tank bioreactor platform provides an effective platform for high-throughput process development. However, the original dual pitched-blade 20 mm impeller and baffles proved sub-optimal for cell therapy candidates that require suspension of microcarriers (e.g. for the culture of adherent human mesenchymal stem cells) or other particles such as activating Dynabeads (R) (e.g. for the culture of human T-cells). We demonstrate the development of a new ambr250 (R) stirred-tank bioreactor vessel which has been designed specifically to improve the suspension of microcarriers/beads and thereby improve the culture of such cellular systems. The new design is unbaffled and has a single, larger elephant ear impeller. We undertook a range of engineering and physical characterizations to determine which vessel and impeller configuration would be most suitable for suspension based on the minimum agitation speed (N-JS) and associated specific power input (P/V)(JS). A vessel (diameter, T, = 60 mm) without baffles and incorporating a single elephant ear impeller (diameter 30 mm and 45 degrees pitch-blade angle) was selected as it had the lowest (P/V)(JS) and therefore potentially, based on Kolmogorov concepts, was the most flexible system. These experimentally-based conclusions were further validated firstly with computational fluid dynamic (CFD) simulations and secondly experimental studies involving the culture of both T-cells with Dynabeads (R) and hMSCs on microcarriers. The new ambr250 (R) stirred-tank bioreactor successfully supported the culture of both cell types, with the T-cell culture demonstrating significant improvements compared to the original ambr250 (R) and the hMSC-microcarrier culture gave significantly higher yields compared with spinner flask cultures. The new ambr250 (R) bioreactor vessel design is an effective process development tool for cell and gene therapy candidates and potentially for autologous manufacture too.
引用
收藏
页码:1103 / 1116
页数:14
相关论文
共 32 条
[1]  
Bareither R., 2015, PHARM BIOPROCESS, V3, P185, DOI DOI 10.4155/PBP.14.64
[2]   Automated Disposable Small Scale Reactor for High Throughput Bioprocess Development: A Proof of Concept Study [J].
Bareither, Rachel ;
Bargh, Neil ;
Oakeshott, Robert ;
Watts, Kathryn ;
Pollard, David .
BIOTECHNOLOGY AND BIOENGINEERING, 2013, 110 (12) :3126-3138
[3]   Establishing the scalable manufacture of primary human T-cells in an automated stirred-tank bioreactor [J].
Costariol, Elena ;
Rotondi, Marco ;
Amini, Arman ;
Hewitt, Christopher J. ;
Nienow, Alvin W. ;
Heathman, Thomas R. J. ;
Micheletti, Martina ;
Rafiq, Qasim A. .
BIOTECHNOLOGY AND BIOENGINEERING, 2019, 116 (10) :2488-2502
[4]   Expansion of human mesenchymal stem/stromal cells (hMSCs) in bioreactors using microcarriers: lessons learnt and what the future holds [J].
Couto, P. Silva ;
Rotondi, M. C. ;
Bersenev, A. ;
Hewitt, C. J. ;
Nienow, A. W. ;
Verter, F. ;
Rafiq, Q. A. .
BIOTECHNOLOGY ADVANCES, 2020, 45
[5]   EFFECTS OF MICROCARRIER CONCENTRATION IN ANIMAL-CELL CULTURE [J].
CROUGHAN, MS ;
HAMEL, JFP ;
WANG, DIC .
BIOTECHNOLOGY AND BIOENGINEERING, 1988, 32 (08) :975-982
[6]   Toward a Clinical-Grade Expansion of Mesenchymal Stem Cells from Human Sources: A Microcarrier-Based Culture System Under Xeno-Free Conditions [J].
dos Santos, Francisco ;
Andrade, Pedro Z. ;
Abecasis, Manuel M. ;
Gimble, Jeffrey M. ;
Chase, Lucas G. ;
Campbell, Andrew M. ;
Boucher, Shayne ;
Vemuri, Mohan C. ;
da Silva, Claudia Lobato ;
Cabral, Joaquim M. S. .
TISSUE ENGINEERING PART C-METHODS, 2011, 17 (12) :1201-1210
[7]  
dos Santos F, 2011, METHODS MOL BIOL, V698, P189, DOI 10.1007/978-1-60761-999-4_15
[8]   Expansion of human mesenchymal stem cells on microcarriers [J].
Hewitt, Christopher J. ;
Lee, Ken ;
Nienow, Alvin W. ;
Thomas, Robert J. ;
Smith, Mark ;
Thomas, Colin R. .
BIOTECHNOLOGY LETTERS, 2011, 33 (11) :2325-2335
[9]   Suspension of microcarriers for cell culture with axial flow impellers [J].
Ibrahim, S ;
Nienow, AW .
CHEMICAL ENGINEERING RESEARCH & DESIGN, 2004, 82 (A9) :1082-1088
[10]  
Ibrahim S, 1996, CHEM ENG RES DES, V74, P679