Cargando…

Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor

Microbioreactors play a critical role in process development as they reduce reagent requirements and can facilitate high‐throughput screening of process parameters and culture conditions. Here, we have demonstrated and explained in detail, for the first time, the amenability of the automated ambr15...

Descripción completa

Detalles Bibliográficos
Autores principales: Rafiq, Qasim A., Hanga, Mariana P., Heathman, Thomas R. J., Coopman, Karen, Nienow, Alvin W., Williams, David J., Hewitt, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615370/
https://www.ncbi.nlm.nih.gov/pubmed/28627713
http://dx.doi.org/10.1002/bit.26359
_version_ 1783266577770086400
author Rafiq, Qasim A.
Hanga, Mariana P.
Heathman, Thomas R. J.
Coopman, Karen
Nienow, Alvin W.
Williams, David J.
Hewitt, Christopher J.
author_facet Rafiq, Qasim A.
Hanga, Mariana P.
Heathman, Thomas R. J.
Coopman, Karen
Nienow, Alvin W.
Williams, David J.
Hewitt, Christopher J.
author_sort Rafiq, Qasim A.
collection PubMed
description Microbioreactors play a critical role in process development as they reduce reagent requirements and can facilitate high‐throughput screening of process parameters and culture conditions. Here, we have demonstrated and explained in detail, for the first time, the amenability of the automated ambr15 cell culture microbioreactor system for the development of scalable adherent human mesenchymal multipotent stromal/stem cell (hMSC) microcarrier culture processes. This was achieved by first improving suspension and mixing of the microcarriers and then improving cell attachment thereby reducing the initial growth lag phase. The latter was achieved by using only 50% of the final working volume of medium for the first 24 h and using an intermittent agitation strategy. These changes resulted in >150% increase in viable cell density after 24 h compared to the original process (no agitation for 24 h and 100% working volume). Using the same methodology as in the ambr15, similar improvements were obtained with larger scale spinner flask studies. Finally, this improved bioprocess methodology based on a serum‐based medium was applied to a serum‐free process in the ambr15, resulting in >250% increase in yield compared to the serum‐based process. At both scales, the agitation used during culture was the minimum required for microcarrier suspension, N(JS). The use of the ambr15, with its improved control compared to the spinner flask, reduced the coefficient of variation on viable cell density in the serum containing medium from 7.65% to 4.08%, and the switch to serum free further reduced these to 1.06–0.54%, respectively. The combination of both serum‐free and automated processing improved the reproducibility more than 10‐fold compared to the serum‐based, manual spinner flask process. The findings of this study demonstrate that the ambr15 microbioreactor is an effective tool for bioprocess development of hMSC microcarrier cultures and that a combination of serum‐free medium, control, and automation improves both process yield and consistency. Biotechnol. Bioeng. 2017;114: 2253–2266. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc.
format Online
Article
Text
id pubmed-5615370
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-56153702017-10-11 Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor Rafiq, Qasim A. Hanga, Mariana P. Heathman, Thomas R. J. Coopman, Karen Nienow, Alvin W. Williams, David J. Hewitt, Christopher J. Biotechnol Bioeng Articles Microbioreactors play a critical role in process development as they reduce reagent requirements and can facilitate high‐throughput screening of process parameters and culture conditions. Here, we have demonstrated and explained in detail, for the first time, the amenability of the automated ambr15 cell culture microbioreactor system for the development of scalable adherent human mesenchymal multipotent stromal/stem cell (hMSC) microcarrier culture processes. This was achieved by first improving suspension and mixing of the microcarriers and then improving cell attachment thereby reducing the initial growth lag phase. The latter was achieved by using only 50% of the final working volume of medium for the first 24 h and using an intermittent agitation strategy. These changes resulted in >150% increase in viable cell density after 24 h compared to the original process (no agitation for 24 h and 100% working volume). Using the same methodology as in the ambr15, similar improvements were obtained with larger scale spinner flask studies. Finally, this improved bioprocess methodology based on a serum‐based medium was applied to a serum‐free process in the ambr15, resulting in >250% increase in yield compared to the serum‐based process. At both scales, the agitation used during culture was the minimum required for microcarrier suspension, N(JS). The use of the ambr15, with its improved control compared to the spinner flask, reduced the coefficient of variation on viable cell density in the serum containing medium from 7.65% to 4.08%, and the switch to serum free further reduced these to 1.06–0.54%, respectively. The combination of both serum‐free and automated processing improved the reproducibility more than 10‐fold compared to the serum‐based, manual spinner flask process. The findings of this study demonstrate that the ambr15 microbioreactor is an effective tool for bioprocess development of hMSC microcarrier cultures and that a combination of serum‐free medium, control, and automation improves both process yield and consistency. Biotechnol. Bioeng. 2017;114: 2253–2266. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2017-07-27 2017-10 /pmc/articles/PMC5615370/ /pubmed/28627713 http://dx.doi.org/10.1002/bit.26359 Text en © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Rafiq, Qasim A.
Hanga, Mariana P.
Heathman, Thomas R. J.
Coopman, Karen
Nienow, Alvin W.
Williams, David J.
Hewitt, Christopher J.
Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title_full Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title_fullStr Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title_full_unstemmed Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title_short Process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
title_sort process development of human multipotent stromal cell microcarrier culture using an automated high‐throughput microbioreactor
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615370/
https://www.ncbi.nlm.nih.gov/pubmed/28627713
http://dx.doi.org/10.1002/bit.26359
work_keys_str_mv AT rafiqqasima processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT hangamarianap processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT heathmanthomasrj processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT coopmankaren processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT nienowalvinw processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT williamsdavidj processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor
AT hewittchristopherj processdevelopmentofhumanmultipotentstromalcellmicrocarriercultureusinganautomatedhighthroughputmicrobioreactor