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An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations

Tools that allow cost‐effective screening of the susceptibility of cell lines to operating conditions which may apply during full scale processing are central to the rapid development of robust processes for cell‐based therapies. In this paper, an ultra scale‐down (USD) device has been developed for...

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Autores principales: Masri, Maria Fernanda, Lawrence, Kate, Wall, Ivan, Hoare, Michael
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/PMC5412937/
https://www.ncbi.nlm.nih.gov/pubmed/28112406
http://dx.doi.org/10.1002/bit.26257
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author Masri, Maria Fernanda
Lawrence, Kate
Wall, Ivan
Hoare, Michael
author_facet Masri, Maria Fernanda
Lawrence, Kate
Wall, Ivan
Hoare, Michael
author_sort Masri, Maria Fernanda
collection PubMed
description Tools that allow cost‐effective screening of the susceptibility of cell lines to operating conditions which may apply during full scale processing are central to the rapid development of robust processes for cell‐based therapies. In this paper, an ultra scale‐down (USD) device has been developed for the characterization of the response of a human cell line to membrane‐based processing, using just a small quantity of cells that is often all that is available at the early discovery stage. The cell line used to develop the measurements was a clinically relevant human fibroblast cell line. The impact was evaluated by cell damage on completion of membrane processing as assessed by trypan blue exclusion and release of intracellular lactate dehydrogenase (LDH). Similar insight was gained from both methods and this allowed the extension of the use of the LDH measurements to examine cell damage as it occurs during processing by a combination of LDH appearance in the permeate and mass balancing of the overall operation. Transmission of LDH was investigated with time of operation and for the two disc speeds investigated (6,000 and 10,000 rpm or ϵ (max) ≈ 1.9 and 13.5 W mL(−1), respectively). As expected, increased energy dissipation rate led to increased transmission as well as significant increases in rate and extent of cell damage. The method developed can be used to test the impact of varying operating conditions and cell lines on cell damage and morphological changes. Biotechnol. Bioeng. 2017;114: 1241–1251. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc.
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spelling pubmed-54129372017-05-19 An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations Masri, Maria Fernanda Lawrence, Kate Wall, Ivan Hoare, Michael Biotechnol Bioeng Articles Tools that allow cost‐effective screening of the susceptibility of cell lines to operating conditions which may apply during full scale processing are central to the rapid development of robust processes for cell‐based therapies. In this paper, an ultra scale‐down (USD) device has been developed for the characterization of the response of a human cell line to membrane‐based processing, using just a small quantity of cells that is often all that is available at the early discovery stage. The cell line used to develop the measurements was a clinically relevant human fibroblast cell line. The impact was evaluated by cell damage on completion of membrane processing as assessed by trypan blue exclusion and release of intracellular lactate dehydrogenase (LDH). Similar insight was gained from both methods and this allowed the extension of the use of the LDH measurements to examine cell damage as it occurs during processing by a combination of LDH appearance in the permeate and mass balancing of the overall operation. Transmission of LDH was investigated with time of operation and for the two disc speeds investigated (6,000 and 10,000 rpm or ϵ (max) ≈ 1.9 and 13.5 W mL(−1), respectively). As expected, increased energy dissipation rate led to increased transmission as well as significant increases in rate and extent of cell damage. The method developed can be used to test the impact of varying operating conditions and cell lines on cell damage and morphological changes. Biotechnol. Bioeng. 2017;114: 1241–1251. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2017-02-23 2017-06 /pmc/articles/PMC5412937/ /pubmed/28112406 http://dx.doi.org/10.1002/bit.26257 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
Masri, Maria Fernanda
Lawrence, Kate
Wall, Ivan
Hoare, Michael
An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title_full An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title_fullStr An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title_full_unstemmed An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title_short An ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
title_sort ultra scale‐down methodology to characterize aspects of the response of human cells to processing by membrane separation operations
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412937/
https://www.ncbi.nlm.nih.gov/pubmed/28112406
http://dx.doi.org/10.1002/bit.26257
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