The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.

The transition from traditional culture methods towards bioreactor based bioprocessing to produce cells in commercially viable quantities for cell therapy applications requires the development of robust methods to ensure the quality of the cells produced. Standard methods for measuring cell quality...

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Main Authors: Marc-Olivier Baradez, Damian Marshall
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3197601?pdf=render
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spelling doaj-5a295562e58b4aa98de4422950b32e7f2020-11-25T00:52:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2610410.1371/journal.pone.0026104The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.Marc-Olivier BaradezDamian MarshallThe transition from traditional culture methods towards bioreactor based bioprocessing to produce cells in commercially viable quantities for cell therapy applications requires the development of robust methods to ensure the quality of the cells produced. Standard methods for measuring cell quality parameters such as viability provide only limited information making process monitoring and optimisation difficult. Here we describe a 3D image-based approach to develop cell distribution maps which can be used to simultaneously measure the number, confluency and morphology of cells attached to microcarriers in a stirred tank bioreactor. The accuracy of the cell distribution measurements is validated using in silico modelling of synthetic image datasets and is shown to have an accuracy >90%. Using the cell distribution mapping process and principal component analysis we show how cell growth can be quantitatively monitored over a 13 day bioreactor culture period and how changes to manufacture processes such as initial cell seeding density can significantly influence cell morphology and the rate at which cells are produced. Taken together, these results demonstrate how image-based analysis can be incorporated in cell quality control processes facilitating the transition towards bioreactor based manufacture for clinical grade cells.http://europepmc.org/articles/PMC3197601?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marc-Olivier Baradez
Damian Marshall
spellingShingle Marc-Olivier Baradez
Damian Marshall
The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
PLoS ONE
author_facet Marc-Olivier Baradez
Damian Marshall
author_sort Marc-Olivier Baradez
title The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
title_short The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
title_full The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
title_fullStr The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
title_full_unstemmed The use of multidimensional image-based analysis to accurately monitor cell growth in 3D bioreactor culture.
title_sort use of multidimensional image-based analysis to accurately monitor cell growth in 3d bioreactor culture.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description The transition from traditional culture methods towards bioreactor based bioprocessing to produce cells in commercially viable quantities for cell therapy applications requires the development of robust methods to ensure the quality of the cells produced. Standard methods for measuring cell quality parameters such as viability provide only limited information making process monitoring and optimisation difficult. Here we describe a 3D image-based approach to develop cell distribution maps which can be used to simultaneously measure the number, confluency and morphology of cells attached to microcarriers in a stirred tank bioreactor. The accuracy of the cell distribution measurements is validated using in silico modelling of synthetic image datasets and is shown to have an accuracy >90%. Using the cell distribution mapping process and principal component analysis we show how cell growth can be quantitatively monitored over a 13 day bioreactor culture period and how changes to manufacture processes such as initial cell seeding density can significantly influence cell morphology and the rate at which cells are produced. Taken together, these results demonstrate how image-based analysis can be incorporated in cell quality control processes facilitating the transition towards bioreactor based manufacture for clinical grade cells.
url http://europepmc.org/articles/PMC3197601?pdf=render
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