The viability of animal cell cultures in bioreactors: Can it be estimated online by using in situ microscopy?
This work aims at checking the possibility of estimating mammalian cell viability from images provided by an in situ microscope (ISM). It was found that images of cells in bioreactors obtained by a high-resolution ISM contain a certain part of cells which exhibits strong morphological similarity wit...
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Veröffentlicht in: | Process biochemistry (1991) 2010-02, Vol.45 (2), p.288-291 |
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creator | Guez, J.S. Cassar, J.Ph Wartelle, F. Dhulster, P. Suhr, H. |
description | This work aims at checking the possibility of estimating mammalian cell viability from images provided by an in situ microscope (ISM). It was found that images of cells in bioreactors obtained by a high-resolution ISM contain a certain part of cells which exhibits strong morphological similarity with images of dying cells or dead cells obtained by epifluorescence. Cell images of this fraction have less homogeneous texture and less smooth borders as compared to regular cells. Modifications of intracellular organelles and irregularities of the plasma membrane can explain such visual features. Therefore, by only using the texture effect, a criterion is proposed in order to distinguish living cells from the other ones. It is based on the variability of the inside part of the image of the cell. A quantitative
estimate of viability (
e
v) is then calculated from a set of images obtained for each sample. The viabilities obtained from the conventional flow cytometry method are inside the 5% confidence interval of these estimations. |
doi_str_mv | 10.1016/j.procbio.2009.09.021 |
format | Article |
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estimate of viability (
e
v) is then calculated from a set of images obtained for each sample. The viabilities obtained from the conventional flow cytometry method are inside the 5% confidence interval of these estimations.</description><identifier>ISSN: 1359-5113</identifier><identifier>EISSN: 1873-3298</identifier><identifier>DOI: 10.1016/j.procbio.2009.09.021</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Animal cell ; Automatic ; Bioreactor ; Biotechnology ; Computer Science ; Culture monitoring ; Engineering Sciences ; Image analysis ; In situ microscopy ; Life Sciences ; Viability</subject><ispartof>Process biochemistry (1991), 2010-02, Vol.45 (2), p.288-291</ispartof><rights>2009 Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-50d2016d7c69f92a29ab7725e4e6fde223add2e48d430f0fcf674a3d8f1ec8583</citedby><cites>FETCH-LOGICAL-c405t-50d2016d7c69f92a29ab7725e4e6fde223add2e48d430f0fcf674a3d8f1ec8583</cites><orcidid>0000-0001-6331-9690 ; 0000-0002-8736-7758</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1359511309003109$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://hal.science/hal-00747794$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Guez, J.S.</creatorcontrib><creatorcontrib>Cassar, J.Ph</creatorcontrib><creatorcontrib>Wartelle, F.</creatorcontrib><creatorcontrib>Dhulster, P.</creatorcontrib><creatorcontrib>Suhr, H.</creatorcontrib><title>The viability of animal cell cultures in bioreactors: Can it be estimated online by using in situ microscopy?</title><title>Process biochemistry (1991)</title><description>This work aims at checking the possibility of estimating mammalian cell viability from images provided by an in situ microscope (ISM). It was found that images of cells in bioreactors obtained by a high-resolution ISM contain a certain part of cells which exhibits strong morphological similarity with images of dying cells or dead cells obtained by epifluorescence. Cell images of this fraction have less homogeneous texture and less smooth borders as compared to regular cells. Modifications of intracellular organelles and irregularities of the plasma membrane can explain such visual features. Therefore, by only using the texture effect, a criterion is proposed in order to distinguish living cells from the other ones. It is based on the variability of the inside part of the image of the cell. A quantitative
estimate of viability (
e
v) is then calculated from a set of images obtained for each sample. The viabilities obtained from the conventional flow cytometry method are inside the 5% confidence interval of these estimations.</description><subject>Animal cell</subject><subject>Automatic</subject><subject>Bioreactor</subject><subject>Biotechnology</subject><subject>Computer Science</subject><subject>Culture monitoring</subject><subject>Engineering Sciences</subject><subject>Image analysis</subject><subject>In situ microscopy</subject><subject>Life Sciences</subject><subject>Viability</subject><issn>1359-5113</issn><issn>1873-3298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkU9rGzEQxZeQQpO0H6GgU6CHdUfS_lMvIZgkLhh6Sc9CK40SmfXKkbQGf_tKOOQaGCQhfvN4b6aqflBYUaDdr93qELwenV8xALEqxehFdUWHntecieEyv3kr6pZS_rW6jnEHwCmlcFXtn1-RHJ0a3eTSiXhL1Oz2aiIap3wsU1oCRuJmkvUDKp18iL_JWs3EJTIiwZgyn9AQP09uRjKeyBLd_FJ6oksL2TsdfNT-cLr7Vn2xaor4_f2-qf49PjyvN_X279Of9f221g20qW7BsBzM9LoTVjDFhBr7nrXYYGcNMsaVMQybwTQcLFhtu75R3AyWoh7agd9UP8-6r2qSh5ANhpP0ysnN_VaWP4C-6XvRHGlmb89sHuLbkuPIvYslvZrRL1HyjjdCdPxTkFEOHVDIYHsGS-4Y0H5YoCDLxuROvm9Mlo3JUqw4uTv3YR7N0WGQUTucNRoXUCdpvPtE4T9BX6JC</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Guez, J.S.</creator><creator>Cassar, J.Ph</creator><creator>Wartelle, F.</creator><creator>Dhulster, P.</creator><creator>Suhr, H.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7U5</scope><scope>F28</scope><scope>L7M</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-6331-9690</orcidid><orcidid>https://orcid.org/0000-0002-8736-7758</orcidid></search><sort><creationdate>20100201</creationdate><title>The viability of animal cell cultures in bioreactors: Can it be estimated online by using in situ microscopy?</title><author>Guez, J.S. ; Cassar, J.Ph ; Wartelle, F. ; Dhulster, P. ; Suhr, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-50d2016d7c69f92a29ab7725e4e6fde223add2e48d430f0fcf674a3d8f1ec8583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animal cell</topic><topic>Automatic</topic><topic>Bioreactor</topic><topic>Biotechnology</topic><topic>Computer Science</topic><topic>Culture monitoring</topic><topic>Engineering Sciences</topic><topic>Image analysis</topic><topic>In situ microscopy</topic><topic>Life Sciences</topic><topic>Viability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guez, J.S.</creatorcontrib><creatorcontrib>Cassar, J.Ph</creatorcontrib><creatorcontrib>Wartelle, F.</creatorcontrib><creatorcontrib>Dhulster, P.</creatorcontrib><creatorcontrib>Suhr, H.</creatorcontrib><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Process biochemistry (1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guez, J.S.</au><au>Cassar, J.Ph</au><au>Wartelle, F.</au><au>Dhulster, P.</au><au>Suhr, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The viability of animal cell cultures in bioreactors: Can it be estimated online by using in situ microscopy?</atitle><jtitle>Process biochemistry (1991)</jtitle><date>2010-02-01</date><risdate>2010</risdate><volume>45</volume><issue>2</issue><spage>288</spage><epage>291</epage><pages>288-291</pages><issn>1359-5113</issn><eissn>1873-3298</eissn><abstract>This work aims at checking the possibility of estimating mammalian cell viability from images provided by an in situ microscope (ISM). It was found that images of cells in bioreactors obtained by a high-resolution ISM contain a certain part of cells which exhibits strong morphological similarity with images of dying cells or dead cells obtained by epifluorescence. Cell images of this fraction have less homogeneous texture and less smooth borders as compared to regular cells. Modifications of intracellular organelles and irregularities of the plasma membrane can explain such visual features. Therefore, by only using the texture effect, a criterion is proposed in order to distinguish living cells from the other ones. It is based on the variability of the inside part of the image of the cell. A quantitative
estimate of viability (
e
v) is then calculated from a set of images obtained for each sample. The viabilities obtained from the conventional flow cytometry method are inside the 5% confidence interval of these estimations.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.procbio.2009.09.021</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0001-6331-9690</orcidid><orcidid>https://orcid.org/0000-0002-8736-7758</orcidid></addata></record> |
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subjects | Animal cell Automatic Bioreactor Biotechnology Computer Science Culture monitoring Engineering Sciences Image analysis In situ microscopy Life Sciences Viability |
title | The viability of animal cell cultures in bioreactors: Can it be estimated online by using in situ microscopy? |
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