Loughborough University
Browse
Inst Repos AmbSC FINAL 13_2_12 Revised Revised FINAL.pdf (436.54 kB)

A novel automated bioreactor for scalable process optimisation of haematopoietic stem cell culture

Download (436.54 kB)
journal contribution
posted on 2013-09-19, 13:22 authored by Elizabeth RatcliffeElizabeth Ratcliffe, Katie GlenKatie Glen, Victoria L. Workman, Adrian J. Stacey, Rob ThomasRob Thomas
Proliferation and differentiation of haematopoietic stem cells (HSCs) from umbilical cord blood at large scale will potentially underpin production of a number of therapeutic cellular products in development, including erythrocytes and platelets. However, to achieve production processes that are scalable and optimised for cost and quality, scaled down development platforms that can define process parameter tolerances and consequent manufacturing controls are essential. We have demonstrated the potential of a new, automated, 24 × 15 mL replicate suspension bioreactor system, with online monitoring and control, to develop an HSC proliferation and differentiation process for erythroid committed cells (CD71+, CD235a+). Cell proliferation was relatively robust to cell density and oxygen levels and reached up to 6 population doublings over 10 days. The maximum suspension culture density for a 48 h total media exchange protocol was established to be in the order of 107 cells/mL. This system will be valuable for the further HSC suspension culture cost reduction and optimisation necessary before the application of conventional stirred tank technology to scaled manufacture of HSC derived products.

History

School

  • Mechanical, Electrical and Manufacturing Engineering

Citation

RATCLIFFE, E. ... et al, 2012. A novel automated bioreactor for scalable process optimisation of haematopoietic stem cell culture. Journal of Biotechnology, 161 (3), pp. 387 - 390.

Publisher

© Elsevier B.V.

Version

  • AM (Accepted Manuscript)

Publication date

2012

Notes

This article was publised in the serial, Journal of Biotechnology [© Elsevier B.V.]. The definitive version is available at: http://dx.doi.org/10.1016/j.jbiotec.2012.06.025

ISSN

0168-1656

Language

  • en