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A scale down process for the development of large volume cryopreservation()
The process of ice formation and propagation during cryopreservation impacts on the post-thaw outcome for a sample. Two processes, either network solidification or progressive solidification, can dominate the water–ice phase transition with network solidification typically present in small sample cr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271741/ https://www.ncbi.nlm.nih.gov/pubmed/25219980 http://dx.doi.org/10.1016/j.cryobiol.2014.09.003 |
_version_ | 1782349664997081088 |
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author | Kilbride, Peter Morris, G. John Milne, Stuart Fuller, Barry Skepper, Jeremy Selden, Clare |
author_facet | Kilbride, Peter Morris, G. John Milne, Stuart Fuller, Barry Skepper, Jeremy Selden, Clare |
author_sort | Kilbride, Peter |
collection | PubMed |
description | The process of ice formation and propagation during cryopreservation impacts on the post-thaw outcome for a sample. Two processes, either network solidification or progressive solidification, can dominate the water–ice phase transition with network solidification typically present in small sample cryo-straws or cryo-vials. Progressive solidification is more often observed in larger volumes or environmental freezing. These different ice phase progressions could have a significant impact on cryopreservation in scale-up and larger volume cryo-banking protocols necessitating their study when considering cell therapy applications. This study determines the impact of these different processes on alginate encapsulated liver spheroids (ELS) as a model system during cryopreservation, and develops a method to replicate these differences in an economical manner. It was found in the current studies that progressive solidification resulted in fewer, but proportionally more viable cells 24 h post-thaw compared with network solidification. The differences between the groups diminished at later time points post-thaw as cells recovered the ability to undertake cell division, with no statistically significant differences seen by either 48 h or 72 h in recovery cultures. Thus progressive solidification itself should not prove a significant hurdle in the search for successful cryopreservation in large volumes. However, some small but significant differences were noted in total viable cell recoveries and functional assessments between samples cooled with either progressive or network solidification, and these require further investigation. |
format | Online Article Text |
id | pubmed-4271741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42717412014-12-22 A scale down process for the development of large volume cryopreservation() Kilbride, Peter Morris, G. John Milne, Stuart Fuller, Barry Skepper, Jeremy Selden, Clare Cryobiology Article The process of ice formation and propagation during cryopreservation impacts on the post-thaw outcome for a sample. Two processes, either network solidification or progressive solidification, can dominate the water–ice phase transition with network solidification typically present in small sample cryo-straws or cryo-vials. Progressive solidification is more often observed in larger volumes or environmental freezing. These different ice phase progressions could have a significant impact on cryopreservation in scale-up and larger volume cryo-banking protocols necessitating their study when considering cell therapy applications. This study determines the impact of these different processes on alginate encapsulated liver spheroids (ELS) as a model system during cryopreservation, and develops a method to replicate these differences in an economical manner. It was found in the current studies that progressive solidification resulted in fewer, but proportionally more viable cells 24 h post-thaw compared with network solidification. The differences between the groups diminished at later time points post-thaw as cells recovered the ability to undertake cell division, with no statistically significant differences seen by either 48 h or 72 h in recovery cultures. Thus progressive solidification itself should not prove a significant hurdle in the search for successful cryopreservation in large volumes. However, some small but significant differences were noted in total viable cell recoveries and functional assessments between samples cooled with either progressive or network solidification, and these require further investigation. Elsevier 2014-12 /pmc/articles/PMC4271741/ /pubmed/25219980 http://dx.doi.org/10.1016/j.cryobiol.2014.09.003 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Article Kilbride, Peter Morris, G. John Milne, Stuart Fuller, Barry Skepper, Jeremy Selden, Clare A scale down process for the development of large volume cryopreservation() |
title | A scale down process for the development of large volume cryopreservation() |
title_full | A scale down process for the development of large volume cryopreservation() |
title_fullStr | A scale down process for the development of large volume cryopreservation() |
title_full_unstemmed | A scale down process for the development of large volume cryopreservation() |
title_short | A scale down process for the development of large volume cryopreservation() |
title_sort | scale down process for the development of large volume cryopreservation() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271741/ https://www.ncbi.nlm.nih.gov/pubmed/25219980 http://dx.doi.org/10.1016/j.cryobiol.2014.09.003 |
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