Scaled‐up production of mammalian neural precursor cell aggregates in computer‐controlled suspension bioreactors

Jane Anne Gilbertson, Arindom Sen, Leo A. Behie, Michael S. Kallos

Biotechnology and Bioengineering · 2006 · 72 citations · 25 references

TL;DR

Neural precursor cells (NPCs) are needed for treating neurological diseases, but their scarcity requires controlled expansion. This study aimed to develop a large‑scale, computer‑controlled bioprocess to expand mammalian NPCs in suspension culture by scaling up existing reactor protocols. The process maintained a volumetric mass transfer coefficient above 1.10 h⁻¹ and limited impeller tip shear stress to 0.30–0.75 Pa while scaling from 125 mL to 500 mL bioreactors. The scaled‑up bioprocess achieved a maximum viable density of 1.2 × 10⁶ cells mL⁻¹, a batch multiplication ratio of 9.1, and preserved NPC characteristics seen at small scale. © 2006 Wiley Periodicals, Inc.

Abstract

Abstract The clinical use of neural precursor cells (NPCs) for the treatment of neurological diseases, such as Parkinson's disease and Huntington's disease, requires overcoming the scarcity of these cells through controlled expansion. The main objective of the present study was to develop a large‐scale computer‐controlled bioprocess for the expansion of mammalian NPCs in suspension culture by scaling up existing reactor protocols. In order to support the oxygen demands of the maximum cell densities achieved, the volumetric mass transfer coefficient was kept above 1.10/h while scaling‐up from small‐scale 125 mL vessels to large‐scale 500 mL bioreactors. In addition, the maximum shear stress at the impeller tip was maintained between 0.30 and 0.75 Pa to reduce damage to the cells. The resulting large‐scale bioprocess achieved maximum viable cell densities of 1.2 × 10 6 cells/mL and a batch multiplication ratio of 9.1. Moreover, the process successfully maintained the NPC characteristics observed in small‐scale studies. © 2006 Wiley Periodicals, Inc.

References

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