Issue 18, 2018

Continuous removal of small nonviable suspended mammalian cells and debris from bioreactors using inertial microfluidics

Abstract

Removing nonviable cells from a cell suspension is crucial in biotechnology and biomanufacturing. Label-free microfluidic cell separation devices based on dielectrophoresis, acoustophoresis, and deterministic lateral displacement are used to remove nonviable cells. However, their volumetric throughputs and test cell concentrations are generally too low to be useful in typical bioreactors in biomanufacturing. In this study, we demonstrate the efficient removal of small (<10 μm) nonviable cells from bioreactors while maintaining viable cells using inertial microfluidic cell sorting devices and characterize their performance. Despite the size overlap between viable and nonviable cell populations, the devices demonstrated 3.5–28.0% dead cell removal efficiency with 88.3–83.6% removal purity as well as 97.8–99.8% live cell retention efficiency at 4 million cells per mL with 80% viability. Cascaded and parallel configurations increased the cell concentration capacity (10 million cells per mL) and volumetric throughput (6–8 mL min−1). The system can be used for the removal of small nonviable cells from a cell suspension during continuous perfusion cell culture operations.

Graphical abstract: Continuous removal of small nonviable suspended mammalian cells and debris from bioreactors using inertial microfluidics

Supplementary files

Article information

Article type
Paper
Submitted
08 Бер 2018
Accepted
31 Лип 2018
First published
31 Лип 2018
This article is Open Access
Creative Commons BY-NC license

Lab Chip, 2018,18, 2826-2837

Continuous removal of small nonviable suspended mammalian cells and debris from bioreactors using inertial microfluidics

T. Kwon, R. Yao, J. P. Hamel and J. Han, Lab Chip, 2018, 18, 2826 DOI: 10.1039/C8LC00250A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements