Impedance spectroscopy flow cytometry: On‐chip label‐free cell differentiation
Background The microfabricated impedance spectroscopy flow cytometer used in this study permits rapid dielectric characterization of a cell population with a simple microfluidic channel. Impedance measurements over a wide frequency range provide information on cell size, membrane capacitance, and cy...
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Veröffentlicht in: | Cytometry. Part A 2005-06, Vol.65A (2), p.124-132 |
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container_title | Cytometry. Part A |
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creator | Cheung, Karen Gawad, Shady Renaud, Philippe |
description | Background
The microfabricated impedance spectroscopy flow cytometer used in this study permits rapid dielectric characterization of a cell population with a simple microfluidic channel. Impedance measurements over a wide frequency range provide information on cell size, membrane capacitance, and cytoplasm conductivity as a function of frequency. The amplitude, opacity, and phase information can be used for discrimination between different cell populations without the use of cell markers.
Methods
Polystyrene beads, red blood cells (RBCs), ghosts, and RBCs fixed in glutaraldehyde were passed through a microfabricated flow cytometer and measured individually by using two simultaneously applied discrete frequencies. The cells were characterized at 1,000 per minute in the frequency range of 350 kHz to 20 MHz.
Results
Cell size was easily measured with submicron accuracy. Polystyrene beads and RBCs were differentiated using opacity. RBCs and ghosts were differentiated using phase information, whereas RBCs and fixed RBCs were differentiated using opacity. RBCs fixed using increasing concentrations of glutaraldehyde showed increasing opacity. This increased opacity was linked to decreased cytoplasm conductivity and decreased membrane capacitance, both resulting from protein cross‐linking.
Conclusions
This work presents label‐free differentiation of cells in an on‐chip flow cytometer based on impedance spectroscopy, which will be a powerful tool for cell characterization. © 2005 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cyto.a.20141 |
format | Article |
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The microfabricated impedance spectroscopy flow cytometer used in this study permits rapid dielectric characterization of a cell population with a simple microfluidic channel. Impedance measurements over a wide frequency range provide information on cell size, membrane capacitance, and cytoplasm conductivity as a function of frequency. The amplitude, opacity, and phase information can be used for discrimination between different cell populations without the use of cell markers.
Methods
Polystyrene beads, red blood cells (RBCs), ghosts, and RBCs fixed in glutaraldehyde were passed through a microfabricated flow cytometer and measured individually by using two simultaneously applied discrete frequencies. The cells were characterized at 1,000 per minute in the frequency range of 350 kHz to 20 MHz.
Results
Cell size was easily measured with submicron accuracy. Polystyrene beads and RBCs were differentiated using opacity. RBCs and ghosts were differentiated using phase information, whereas RBCs and fixed RBCs were differentiated using opacity. RBCs fixed using increasing concentrations of glutaraldehyde showed increasing opacity. This increased opacity was linked to decreased cytoplasm conductivity and decreased membrane capacitance, both resulting from protein cross‐linking.
Conclusions
This work presents label‐free differentiation of cells in an on‐chip flow cytometer based on impedance spectroscopy, which will be a powerful tool for cell characterization. © 2005 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4922</identifier><identifier>EISSN: 1552-4930</identifier><identifier>DOI: 10.1002/cyto.a.20141</identifier><identifier>PMID: 15825181</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Cell Differentiation ; dielectric spectroscopy ; Electric Conductivity ; Electric Impedance ; Electrodes ; Erythrocyte Membrane - metabolism ; Erythrocyte Membrane - physiology ; Erythrocytes - cytology ; Flow Cytometry - methods ; Humans ; impedance characterization ; label free ; microfabricated flow cytometer ; Platinum ; Polystyrenes - chemistry ; Polystyrenes - metabolism ; Spectrophotometry - methods ; Titanium</subject><ispartof>Cytometry. Part A, 2005-06, Vol.65A (2), p.124-132</ispartof><rights>Copyright © 2005 Wiley‐Liss, Inc.</rights><rights>Copyright (c) 2005 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4371-cf97ef11309be8e15a9474e1cecdcb465e7d3dfdd9bd7c78fa8bfbc91f67a1fa3</citedby><cites>FETCH-LOGICAL-c4371-cf97ef11309be8e15a9474e1cecdcb465e7d3dfdd9bd7c78fa8bfbc91f67a1fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcyto.a.20141$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcyto.a.20141$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15825181$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheung, Karen</creatorcontrib><creatorcontrib>Gawad, Shady</creatorcontrib><creatorcontrib>Renaud, Philippe</creatorcontrib><title>Impedance spectroscopy flow cytometry: On‐chip label‐free cell differentiation</title><title>Cytometry. Part A</title><addtitle>Cytometry A</addtitle><description>Background
The microfabricated impedance spectroscopy flow cytometer used in this study permits rapid dielectric characterization of a cell population with a simple microfluidic channel. Impedance measurements over a wide frequency range provide information on cell size, membrane capacitance, and cytoplasm conductivity as a function of frequency. The amplitude, opacity, and phase information can be used for discrimination between different cell populations without the use of cell markers.
Methods
Polystyrene beads, red blood cells (RBCs), ghosts, and RBCs fixed in glutaraldehyde were passed through a microfabricated flow cytometer and measured individually by using two simultaneously applied discrete frequencies. The cells were characterized at 1,000 per minute in the frequency range of 350 kHz to 20 MHz.
Results
Cell size was easily measured with submicron accuracy. Polystyrene beads and RBCs were differentiated using opacity. RBCs and ghosts were differentiated using phase information, whereas RBCs and fixed RBCs were differentiated using opacity. RBCs fixed using increasing concentrations of glutaraldehyde showed increasing opacity. This increased opacity was linked to decreased cytoplasm conductivity and decreased membrane capacitance, both resulting from protein cross‐linking.
Conclusions
This work presents label‐free differentiation of cells in an on‐chip flow cytometer based on impedance spectroscopy, which will be a powerful tool for cell characterization. © 2005 Wiley‐Liss, Inc.</description><subject>Cell Differentiation</subject><subject>dielectric spectroscopy</subject><subject>Electric Conductivity</subject><subject>Electric Impedance</subject><subject>Electrodes</subject><subject>Erythrocyte Membrane - metabolism</subject><subject>Erythrocyte Membrane - physiology</subject><subject>Erythrocytes - cytology</subject><subject>Flow Cytometry - methods</subject><subject>Humans</subject><subject>impedance characterization</subject><subject>label free</subject><subject>microfabricated flow cytometer</subject><subject>Platinum</subject><subject>Polystyrenes - chemistry</subject><subject>Polystyrenes - metabolism</subject><subject>Spectrophotometry - methods</subject><subject>Titanium</subject><issn>1552-4922</issn><issn>1552-4930</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1Lw0AQhhdRbK3ePEtOnkzd2U26iTcpfhQKBakHT8tmdxYj-XI3peTmT_A3-ktMbNGbp5mBh4d5X0LOgU6BUnatu7aeqimjEMEBGUMcszBKOT383RkbkRPv3yjlMeXsmIwgTlgMCYzJ06Js0KhKY-Ab1K2rva6bLrBFvQ0GdYmt626CVfX18alf8yYoVIZFf1iHGGgsisDk1qLDqs1Vm9fVKTmyqvB4tp8T8nx_t54_hsvVw2J-uwx1xAWE2qYCLQCnaYYJQqzSSEQIGrXRWTSLURhurDFpZoQWiVVJZjOdgp0JBVbxCbnceRtXv2_Qt7LM_fCQqrDeeDkTScog4j14tQN1n847tLJxealcJ4HKoUM5BJVK_nTY4xd77yYr0fzB-9J6gO-AbV5g969Mzl_Wq532G3ZFgms</recordid><startdate>200506</startdate><enddate>200506</enddate><creator>Cheung, Karen</creator><creator>Gawad, Shady</creator><creator>Renaud, Philippe</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>7X8</scope></search><sort><creationdate>200506</creationdate><title>Impedance spectroscopy flow cytometry: On‐chip label‐free cell differentiation</title><author>Cheung, Karen ; Gawad, Shady ; Renaud, Philippe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4371-cf97ef11309be8e15a9474e1cecdcb465e7d3dfdd9bd7c78fa8bfbc91f67a1fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Cell Differentiation</topic><topic>dielectric spectroscopy</topic><topic>Electric Conductivity</topic><topic>Electric Impedance</topic><topic>Electrodes</topic><topic>Erythrocyte Membrane - metabolism</topic><topic>Erythrocyte Membrane - physiology</topic><topic>Erythrocytes - cytology</topic><topic>Flow Cytometry - methods</topic><topic>Humans</topic><topic>impedance characterization</topic><topic>label free</topic><topic>microfabricated flow cytometer</topic><topic>Platinum</topic><topic>Polystyrenes - chemistry</topic><topic>Polystyrenes - metabolism</topic><topic>Spectrophotometry - methods</topic><topic>Titanium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheung, Karen</creatorcontrib><creatorcontrib>Gawad, Shady</creatorcontrib><creatorcontrib>Renaud, Philippe</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytometry. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheung, Karen</au><au>Gawad, Shady</au><au>Renaud, Philippe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impedance spectroscopy flow cytometry: On‐chip label‐free cell differentiation</atitle><jtitle>Cytometry. Part A</jtitle><addtitle>Cytometry A</addtitle><date>2005-06</date><risdate>2005</risdate><volume>65A</volume><issue>2</issue><spage>124</spage><epage>132</epage><pages>124-132</pages><issn>1552-4922</issn><eissn>1552-4930</eissn><abstract>Background
The microfabricated impedance spectroscopy flow cytometer used in this study permits rapid dielectric characterization of a cell population with a simple microfluidic channel. Impedance measurements over a wide frequency range provide information on cell size, membrane capacitance, and cytoplasm conductivity as a function of frequency. The amplitude, opacity, and phase information can be used for discrimination between different cell populations without the use of cell markers.
Methods
Polystyrene beads, red blood cells (RBCs), ghosts, and RBCs fixed in glutaraldehyde were passed through a microfabricated flow cytometer and measured individually by using two simultaneously applied discrete frequencies. The cells were characterized at 1,000 per minute in the frequency range of 350 kHz to 20 MHz.
Results
Cell size was easily measured with submicron accuracy. Polystyrene beads and RBCs were differentiated using opacity. RBCs and ghosts were differentiated using phase information, whereas RBCs and fixed RBCs were differentiated using opacity. RBCs fixed using increasing concentrations of glutaraldehyde showed increasing opacity. This increased opacity was linked to decreased cytoplasm conductivity and decreased membrane capacitance, both resulting from protein cross‐linking.
Conclusions
This work presents label‐free differentiation of cells in an on‐chip flow cytometer based on impedance spectroscopy, which will be a powerful tool for cell characterization. © 2005 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15825181</pmid><doi>10.1002/cyto.a.20141</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Differentiation dielectric spectroscopy Electric Conductivity Electric Impedance Electrodes Erythrocyte Membrane - metabolism Erythrocyte Membrane - physiology Erythrocytes - cytology Flow Cytometry - methods Humans impedance characterization label free microfabricated flow cytometer Platinum Polystyrenes - chemistry Polystyrenes - metabolism Spectrophotometry - methods Titanium |
title | Impedance spectroscopy flow cytometry: On‐chip label‐free cell differentiation |
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