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Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation

Suspension culture is an essential large-scale cell culture technique for biopharmaceutical development and regenerative medicine. To transition from monolayer culture on the culture surface of a flask to suspension culture in a bioreactor, a pre-specified cell number must first be reached. During t...

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Autores principales: Fujii, Genichiro, Kurashina, Yuta, Terao, Yusuke, Azuma, Tetsushi, Morikawa, Akira, Kodeki, Kazuhide, Takahara, Osamu, Takemura, Kenjiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902488/
https://www.ncbi.nlm.nih.gov/pubmed/33607592
http://dx.doi.org/10.1016/j.ultsonch.2021.105488
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author Fujii, Genichiro
Kurashina, Yuta
Terao, Yusuke
Azuma, Tetsushi
Morikawa, Akira
Kodeki, Kazuhide
Takahara, Osamu
Takemura, Kenjiro
author_facet Fujii, Genichiro
Kurashina, Yuta
Terao, Yusuke
Azuma, Tetsushi
Morikawa, Akira
Kodeki, Kazuhide
Takahara, Osamu
Takemura, Kenjiro
author_sort Fujii, Genichiro
collection PubMed
description Suspension culture is an essential large-scale cell culture technique for biopharmaceutical development and regenerative medicine. To transition from monolayer culture on the culture surface of a flask to suspension culture in a bioreactor, a pre-specified cell number must first be reached. During this period of preparation for suspension culture, static suspension culture in a flask is generally performed because the medium volume is not large enough to use a paddle to circulate the medium. However, drawbacks to this static method include cell sedimentation, leading to high cell density near the bottom and resulting in oxygen and nutrient deficiencies. Here, we propose a suspension culture method with acoustic streaming induced by ultrasonic waves in a T-flask to create a more homogeneous distribution of oxygen, nutrients, and waste products during the preparation period preceding large-scale suspension culture in a bioreactor. To demonstrate the performance of the ultrasonic method, Chinese hamster ovary cells were cultured for 72 h. Results showed that, on average, the cell proliferation was improved by 40% compared with the static method. Thus, the culture time required to achieve a 1000-fold increase could be reduced by 32 h (a 14% reduction) compared with the static method. Furthermore, the ultrasonic irradiation did not compromise the metabolic activity of the cells cultured using the ultrasonic method. These results demonstrate the effectiveness of the ultrasonic method for accelerating the transition to large-scale suspension culture.
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spelling pubmed-79024882021-03-03 Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation Fujii, Genichiro Kurashina, Yuta Terao, Yusuke Azuma, Tetsushi Morikawa, Akira Kodeki, Kazuhide Takahara, Osamu Takemura, Kenjiro Ultrason Sonochem Original Research Article Suspension culture is an essential large-scale cell culture technique for biopharmaceutical development and regenerative medicine. To transition from monolayer culture on the culture surface of a flask to suspension culture in a bioreactor, a pre-specified cell number must first be reached. During this period of preparation for suspension culture, static suspension culture in a flask is generally performed because the medium volume is not large enough to use a paddle to circulate the medium. However, drawbacks to this static method include cell sedimentation, leading to high cell density near the bottom and resulting in oxygen and nutrient deficiencies. Here, we propose a suspension culture method with acoustic streaming induced by ultrasonic waves in a T-flask to create a more homogeneous distribution of oxygen, nutrients, and waste products during the preparation period preceding large-scale suspension culture in a bioreactor. To demonstrate the performance of the ultrasonic method, Chinese hamster ovary cells were cultured for 72 h. Results showed that, on average, the cell proliferation was improved by 40% compared with the static method. Thus, the culture time required to achieve a 1000-fold increase could be reduced by 32 h (a 14% reduction) compared with the static method. Furthermore, the ultrasonic irradiation did not compromise the metabolic activity of the cells cultured using the ultrasonic method. These results demonstrate the effectiveness of the ultrasonic method for accelerating the transition to large-scale suspension culture. Elsevier 2021-02-10 /pmc/articles/PMC7902488/ /pubmed/33607592 http://dx.doi.org/10.1016/j.ultsonch.2021.105488 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
Fujii, Genichiro
Kurashina, Yuta
Terao, Yusuke
Azuma, Tetsushi
Morikawa, Akira
Kodeki, Kazuhide
Takahara, Osamu
Takemura, Kenjiro
Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title_full Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title_fullStr Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title_full_unstemmed Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title_short Suspension culture in a T-flask with acoustic flow induced by ultrasonic irradiation
title_sort suspension culture in a t-flask with acoustic flow induced by ultrasonic irradiation
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902488/
https://www.ncbi.nlm.nih.gov/pubmed/33607592
http://dx.doi.org/10.1016/j.ultsonch.2021.105488
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