Oxygen supply for CHO cells immobilized on a packed-bed of Fibra-Cel® disks
Packed‐bed bioreactors (PBR) have proven to be efficient systems to culture mammalian cells at very high cell density in perfusion mode, thus leading to very high volumetric productivity. However, the immobilized cells must be continuously supplied with all nutrients in sufficient quantities to rema...
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Veröffentlicht in: | Biotechnology and bioengineering 2006-03, Vol.93 (4), p.791-800 |
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description | Packed‐bed bioreactors (PBR) have proven to be efficient systems to culture mammalian cells at very high cell density in perfusion mode, thus leading to very high volumetric productivity. However, the immobilized cells must be continuously supplied with all nutrients in sufficient quantities to remain viable and productive over the full duration of the perfusion culture. Among all nutrients, oxygen is the most critical since it is present at very low concentration due to its low solubility in cell culture medium. This work presents the development of a model for oxygenation in a packed‐bed bioreactor system. The experimental system used to develop the model was a packed‐bed of Fibra‐Cel® disk carriers used to cultivate Chinese Hamster Ovary cells at high density (∼6.1 × 107 cell/mL) in perfusion mode. With the help of this model, it was possible to identify if a PBR system is operated in optimal or sub‐optimal conditions. Using the model, two options were proposed, which could improve the performance of the basal system by about twofold, that is, by increasing the density of immobilized cells per carrier volume from 6.1 × 107 to 1.2 × 108 cell/mL, or by increasing the packed‐bed height from 0.2 to 0.4 m. Both strategies would be rather simple to test and implement in the packed‐bed bioreactor system used for this study. As a result, it would be possible to achieve a substantial improvement of about twofold higher productivity as compared with the basal conditions. © 2005 Wiley Periodicals, Inc. |
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However, the immobilized cells must be continuously supplied with all nutrients in sufficient quantities to remain viable and productive over the full duration of the perfusion culture. Among all nutrients, oxygen is the most critical since it is present at very low concentration due to its low solubility in cell culture medium. This work presents the development of a model for oxygenation in a packed‐bed bioreactor system. The experimental system used to develop the model was a packed‐bed of Fibra‐Cel® disk carriers used to cultivate Chinese Hamster Ovary cells at high density (∼6.1 × 107 cell/mL) in perfusion mode. With the help of this model, it was possible to identify if a PBR system is operated in optimal or sub‐optimal conditions. Using the model, two options were proposed, which could improve the performance of the basal system by about twofold, that is, by increasing the density of immobilized cells per carrier volume from 6.1 × 107 to 1.2 × 108 cell/mL, or by increasing the packed‐bed height from 0.2 to 0.4 m. Both strategies would be rather simple to test and implement in the packed‐bed bioreactor system used for this study. As a result, it would be possible to achieve a substantial improvement of about twofold higher productivity as compared with the basal conditions. © 2005 Wiley Periodicals, Inc.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.20766</identifier><identifier>PMID: 16358288</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Biological and medical sciences ; Bioreactors ; Biotechnology ; Cell culture ; Cells, Immobilized ; CHO ; CHO Cells - metabolism ; Cricetinae ; Cricetulus ; Fibra-Cel ; Fundamental and applied biological sciences. 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Bioeng</addtitle><description>Packed‐bed bioreactors (PBR) have proven to be efficient systems to culture mammalian cells at very high cell density in perfusion mode, thus leading to very high volumetric productivity. However, the immobilized cells must be continuously supplied with all nutrients in sufficient quantities to remain viable and productive over the full duration of the perfusion culture. Among all nutrients, oxygen is the most critical since it is present at very low concentration due to its low solubility in cell culture medium. This work presents the development of a model for oxygenation in a packed‐bed bioreactor system. The experimental system used to develop the model was a packed‐bed of Fibra‐Cel® disk carriers used to cultivate Chinese Hamster Ovary cells at high density (∼6.1 × 107 cell/mL) in perfusion mode. With the help of this model, it was possible to identify if a PBR system is operated in optimal or sub‐optimal conditions. Using the model, two options were proposed, which could improve the performance of the basal system by about twofold, that is, by increasing the density of immobilized cells per carrier volume from 6.1 × 107 to 1.2 × 108 cell/mL, or by increasing the packed‐bed height from 0.2 to 0.4 m. Both strategies would be rather simple to test and implement in the packed‐bed bioreactor system used for this study. As a result, it would be possible to achieve a substantial improvement of about twofold higher productivity as compared with the basal conditions. © 2005 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bioreactors</subject><subject>Biotechnology</subject><subject>Cell culture</subject><subject>Cells, Immobilized</subject><subject>CHO</subject><subject>CHO Cells - metabolism</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Fibra-Cel</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Mammals</subject><subject>Models, Theoretical</subject><subject>Nutrients</subject><subject>Oxygen</subject><subject>Oxygen - metabolism</subject><subject>Oxygenation</subject><subject>packed-bed</subject><subject>perfusion</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10NtKHDEYB_BQWuqqvegLlFBQ8GI0h_mSmcu6HmHp3qi9DEkmU-LOqckOun2oPoRPZra7KhRKLkLg9x3yR-gzJceUEHZi_PKYESnEOzShpJQZYSV5jyaEEJFxKNkO2o3xPj1lIcRHtEMFh4IVxQTN5o-rn67DcRyGZoXrPuDp1Rxb1zQR-7btjW_8b1fhvsMaD9ouXJWZ9bvGF94EnU1d8_QHVz4u4j76UOsmuk_bew_dXpzfTK-y2fzyevptltmcFiKrJdRCAAdwltGy1C4HpqWhQIBKk4POCa2oBWI0K4zUIElRy7JKRZaD43vocNN3CP2v0cWlan1cr6w7149RCZmOYJDg13_gfT-GLu2mGOVSUM7KhI42yIY-xuBqNQTf6rBSlKh1virlq_7mm-yXbcPRtK56k9tAEzjYAh2tbuqgO-vjm5OQU5A8uZONe_CNW_1_ojq9vnkZnW0qfFy6x9cKHRbpv1yC-vH9Up0VFO54eacEfwbSWZ2t</recordid><startdate>20060305</startdate><enddate>20060305</enddate><creator>Meuwly, F.</creator><creator>Loviat, F.</creator><creator>Ruffieux, P.-A.</creator><creator>Bernard, A.R.</creator><creator>Kadouri, A.</creator><creator>von Stockar, U.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20060305</creationdate><title>Oxygen supply for CHO cells immobilized on a packed-bed of Fibra-Cel® disks</title><author>Meuwly, F. ; Loviat, F. ; Ruffieux, P.-A. ; Bernard, A.R. ; Kadouri, A. ; von Stockar, U.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4186-f75f665355ec2199ae452a7b150517b45a401d1c50ba28b7a5708f79d665c35e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bioreactors</topic><topic>Biotechnology</topic><topic>Cell culture</topic><topic>Cells, Immobilized</topic><topic>CHO</topic><topic>CHO Cells - metabolism</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Fibra-Cel</topic><topic>Fundamental and applied biological sciences. 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Bioeng</addtitle><date>2006-03-05</date><risdate>2006</risdate><volume>93</volume><issue>4</issue><spage>791</spage><epage>800</epage><pages>791-800</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>Packed‐bed bioreactors (PBR) have proven to be efficient systems to culture mammalian cells at very high cell density in perfusion mode, thus leading to very high volumetric productivity. However, the immobilized cells must be continuously supplied with all nutrients in sufficient quantities to remain viable and productive over the full duration of the perfusion culture. Among all nutrients, oxygen is the most critical since it is present at very low concentration due to its low solubility in cell culture medium. This work presents the development of a model for oxygenation in a packed‐bed bioreactor system. The experimental system used to develop the model was a packed‐bed of Fibra‐Cel® disk carriers used to cultivate Chinese Hamster Ovary cells at high density (∼6.1 × 107 cell/mL) in perfusion mode. With the help of this model, it was possible to identify if a PBR system is operated in optimal or sub‐optimal conditions. Using the model, two options were proposed, which could improve the performance of the basal system by about twofold, that is, by increasing the density of immobilized cells per carrier volume from 6.1 × 107 to 1.2 × 108 cell/mL, or by increasing the packed‐bed height from 0.2 to 0.4 m. Both strategies would be rather simple to test and implement in the packed‐bed bioreactor system used for this study. As a result, it would be possible to achieve a substantial improvement of about twofold higher productivity as compared with the basal conditions. © 2005 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16358288</pmid><doi>10.1002/bit.20766</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Bioreactors Biotechnology Cell culture Cells, Immobilized CHO CHO Cells - metabolism Cricetinae Cricetulus Fibra-Cel Fundamental and applied biological sciences. Psychology Mammals Models, Theoretical Nutrients Oxygen Oxygen - metabolism Oxygenation packed-bed perfusion |
title | Oxygen supply for CHO cells immobilized on a packed-bed of Fibra-Cel® disks |
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