A portable microelectrode array recording system incorporating cultured neuronal networks for neurotoxin detection
Cultured neuronal networks, which have the capacity to respond to a wide range of neuroactive compounds, have been suggested to be useful for both screening known analytes and unknown compounds for acute neuropharmacologic effects. Extracellular recording from cultured neuronal networks provides a m...
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creator | Pancrazio, Joseph J. Gray, Samuel A. Shubin, Yura S. Kulagina, Nadezhda Cuttino, David S. Shaffer, Kara M. Eisemann, Kevin Curran, Anthony Zim, Bret Gross, Guenter W. O'Shaughnessy, Thomas J. |
description | Cultured neuronal networks, which have the capacity to respond to a wide range of neuroactive compounds, have been suggested to be useful for both screening known analytes and unknown compounds for acute neuropharmacologic effects. Extracellular recording from cultured neuronal networks provides a means for extracting physiologically relevant activity, i.e. action potential firing, in a noninvasive manner conducive for long-term measurements. Previous work from our laboratory described prototype portable systems capable of high signal-to-noise extracellular recordings from cardiac myocytes. The present work describes a portable system tailored to monitoring neuronal extracellular potentials that readily incorporates standardized microelectrode arrays developed by and in use at the University of North Texas. This system utilizes low noise amplifier and filter boards, a two-stage thermal control system with integrated fluidics and a graphical user interface for data acquisition and control implemented on a personal computer. Wherever possible, off-the-shelf components have been utilized for system design and fabrication. During use with cultured neuronal networks, the system typically exhibits input referred noise levels of only 4–6 μV
RMS, such that extracellular potentials exceeding 40 μV can be readily resolved. A flow rate of up to 1 ml/min was achieved while the cell recording chamber temperature was maintained within a range of 36–37
°C. To demonstrate the capability of this system to resolve small extracellular potentials, pharmacological experiments with cultured neuronal networks have been performed using ion channel blockers, tetrodotoxin and tityustoxin. The implications of the experiments for neurotoxin detection are discussed. |
doi_str_mv | 10.1016/S0956-5663(03)00092-7 |
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RMS, such that extracellular potentials exceeding 40 μV can be readily resolved. A flow rate of up to 1 ml/min was achieved while the cell recording chamber temperature was maintained within a range of 36–37
°C. To demonstrate the capability of this system to resolve small extracellular potentials, pharmacological experiments with cultured neuronal networks have been performed using ion channel blockers, tetrodotoxin and tityustoxin. The implications of the experiments for neurotoxin detection are discussed.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/S0956-5663(03)00092-7</identifier><identifier>PMID: 12896834</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Action Potentials - drug effects ; Action Potentials - physiology ; Amplifier ; Animals ; Array ; Biological and medical sciences ; Biosensing Techniques - instrumentation ; Biosensing Techniques - methods ; Biosensor ; Biosensors ; Biotechnology ; Cell Culture Techniques - instrumentation ; Cell Culture Techniques - methods ; Cells, Cultured ; Dose-Response Relationship, Drug ; Electrophysiology - instrumentation ; Electrophysiology - methods ; Environmental Exposure - analysis ; Equipment Design ; Equipment Failure Analysis ; Extracellular recording ; Feasibility Studies ; Fundamental and applied biological sciences. Psychology ; Information Storage and Retrieval - methods ; ion channel blockers ; Methods. Procedures. Technologies ; Mice ; Mice, Inbred ICR ; Microelectrode array ; Microelectrodes ; Miniaturization ; Nerve Net - drug effects ; Nerve Net - physiology ; Neurotoxins - analysis ; Neurotoxins - poisoning ; Portable ; Primary neuronal cultures ; Reproducibility of Results ; Scorpion Venoms - analysis ; Scorpion Venoms - poisoning ; Sensitivity and Specificity ; signal-to-noise ratio ; tetrodotoxin ; Tetrodotoxin - analysis ; Tetrodotoxin - poisoning ; tityustoxin ; User-Computer Interface ; Various methods and equipments</subject><ispartof>Biosensors & bioelectronics, 2003-10, Vol.18 (11), p.1339-1347</ispartof><rights>2003 Elsevier Science B.V.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-75985af0bfe6659635028079981413b03b82712f40e93f20df5860997dd479d3</citedby><cites>FETCH-LOGICAL-c490t-75985af0bfe6659635028079981413b03b82712f40e93f20df5860997dd479d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0956-5663(03)00092-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15062874$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12896834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pancrazio, Joseph J.</creatorcontrib><creatorcontrib>Gray, Samuel A.</creatorcontrib><creatorcontrib>Shubin, Yura S.</creatorcontrib><creatorcontrib>Kulagina, Nadezhda</creatorcontrib><creatorcontrib>Cuttino, David S.</creatorcontrib><creatorcontrib>Shaffer, Kara M.</creatorcontrib><creatorcontrib>Eisemann, Kevin</creatorcontrib><creatorcontrib>Curran, Anthony</creatorcontrib><creatorcontrib>Zim, Bret</creatorcontrib><creatorcontrib>Gross, Guenter W.</creatorcontrib><creatorcontrib>O'Shaughnessy, Thomas J.</creatorcontrib><title>A portable microelectrode array recording system incorporating cultured neuronal networks for neurotoxin detection</title><title>Biosensors & bioelectronics</title><addtitle>Biosens Bioelectron</addtitle><description>Cultured neuronal networks, which have the capacity to respond to a wide range of neuroactive compounds, have been suggested to be useful for both screening known analytes and unknown compounds for acute neuropharmacologic effects. Extracellular recording from cultured neuronal networks provides a means for extracting physiologically relevant activity, i.e. action potential firing, in a noninvasive manner conducive for long-term measurements. Previous work from our laboratory described prototype portable systems capable of high signal-to-noise extracellular recordings from cardiac myocytes. The present work describes a portable system tailored to monitoring neuronal extracellular potentials that readily incorporates standardized microelectrode arrays developed by and in use at the University of North Texas. This system utilizes low noise amplifier and filter boards, a two-stage thermal control system with integrated fluidics and a graphical user interface for data acquisition and control implemented on a personal computer. Wherever possible, off-the-shelf components have been utilized for system design and fabrication. During use with cultured neuronal networks, the system typically exhibits input referred noise levels of only 4–6 μV
RMS, such that extracellular potentials exceeding 40 μV can be readily resolved. A flow rate of up to 1 ml/min was achieved while the cell recording chamber temperature was maintained within a range of 36–37
°C. To demonstrate the capability of this system to resolve small extracellular potentials, pharmacological experiments with cultured neuronal networks have been performed using ion channel blockers, tetrodotoxin and tityustoxin. The implications of the experiments for neurotoxin detection are discussed.</description><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>Amplifier</subject><subject>Animals</subject><subject>Array</subject><subject>Biological and medical sciences</subject><subject>Biosensing Techniques - instrumentation</subject><subject>Biosensing Techniques - methods</subject><subject>Biosensor</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Cell Culture Techniques - instrumentation</subject><subject>Cell Culture Techniques - methods</subject><subject>Cells, Cultured</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electrophysiology - instrumentation</subject><subject>Electrophysiology - methods</subject><subject>Environmental Exposure - analysis</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Extracellular recording</subject><subject>Feasibility Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Information Storage and Retrieval - methods</subject><subject>ion channel blockers</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Microelectrode array</subject><subject>Microelectrodes</subject><subject>Miniaturization</subject><subject>Nerve Net - drug effects</subject><subject>Nerve Net - physiology</subject><subject>Neurotoxins - analysis</subject><subject>Neurotoxins - poisoning</subject><subject>Portable</subject><subject>Primary neuronal cultures</subject><subject>Reproducibility of Results</subject><subject>Scorpion Venoms - analysis</subject><subject>Scorpion Venoms - poisoning</subject><subject>Sensitivity and Specificity</subject><subject>signal-to-noise ratio</subject><subject>tetrodotoxin</subject><subject>Tetrodotoxin - analysis</subject><subject>Tetrodotoxin - poisoning</subject><subject>tityustoxin</subject><subject>User-Computer Interface</subject><subject>Various methods and equipments</subject><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1rFTEUhoNY7LX6E5TZWHQxejKZfK2kFD8KBRd2HzLJGYnOTK5JRr3_vhnvxS6FQMLL854kDyEvKLylQMW7r6C5aLkQ7DWwNwCgu1Y-IjuqJGv7jvHHZPcPOSdPc_5eIUk1PCHntFNaKNbvSLpq9jEVO0zYzMGliBO6kqLHxqZkD01CF5MPy7cmH3LBuQlLDWrHli1061TWhL5ZcE1xsVM9lN8x_cjNGNMxLfFPWBqPpU4OcXlGzkY7ZXx-2i_I3ccPd9ef29svn26ur25b12soreRacTvCMKIQXAvGoVMgtVa0p2wANqhO0m7sATUbO_AjVwK0lt73Unt2QS6PY_cp_lwxFzOH7HCa7IJxzYYqzTrGZAX5Eay_zznhaPYpzDYdDAWzuTZ_XZtNpIG6Ntdm6708XbAOM_qH1kluBV6dAJudncZkFxfyA8dBdEpu3Psjh9XGr4DJZBdwcehDtV-Mj-E_T7kH9h6dNg</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Pancrazio, Joseph J.</creator><creator>Gray, Samuel A.</creator><creator>Shubin, Yura S.</creator><creator>Kulagina, Nadezhda</creator><creator>Cuttino, David S.</creator><creator>Shaffer, Kara M.</creator><creator>Eisemann, Kevin</creator><creator>Curran, Anthony</creator><creator>Zim, Bret</creator><creator>Gross, Guenter W.</creator><creator>O'Shaughnessy, Thomas J.</creator><general>Elsevier B.V</general><general>Elsevier Science</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20031001</creationdate><title>A portable microelectrode array recording system incorporating cultured neuronal networks for neurotoxin detection</title><author>Pancrazio, Joseph J. ; Gray, Samuel A. ; Shubin, Yura S. ; Kulagina, Nadezhda ; Cuttino, David S. ; Shaffer, Kara M. ; Eisemann, Kevin ; Curran, Anthony ; Zim, Bret ; Gross, Guenter W. ; O'Shaughnessy, Thomas J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-75985af0bfe6659635028079981413b03b82712f40e93f20df5860997dd479d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>Amplifier</topic><topic>Animals</topic><topic>Array</topic><topic>Biological and medical sciences</topic><topic>Biosensing Techniques - instrumentation</topic><topic>Biosensing Techniques - methods</topic><topic>Biosensor</topic><topic>Biosensors</topic><topic>Biotechnology</topic><topic>Cell Culture Techniques - instrumentation</topic><topic>Cell Culture Techniques - methods</topic><topic>Cells, Cultured</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electrophysiology - instrumentation</topic><topic>Electrophysiology - methods</topic><topic>Environmental Exposure - analysis</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Extracellular recording</topic><topic>Feasibility Studies</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Information Storage and Retrieval - methods</topic><topic>ion channel blockers</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Microelectrode array</topic><topic>Microelectrodes</topic><topic>Miniaturization</topic><topic>Nerve Net - drug effects</topic><topic>Nerve Net - physiology</topic><topic>Neurotoxins - analysis</topic><topic>Neurotoxins - poisoning</topic><topic>Portable</topic><topic>Primary neuronal cultures</topic><topic>Reproducibility of Results</topic><topic>Scorpion Venoms - analysis</topic><topic>Scorpion Venoms - poisoning</topic><topic>Sensitivity and Specificity</topic><topic>signal-to-noise ratio</topic><topic>tetrodotoxin</topic><topic>Tetrodotoxin - analysis</topic><topic>Tetrodotoxin - poisoning</topic><topic>tityustoxin</topic><topic>User-Computer Interface</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pancrazio, Joseph J.</creatorcontrib><creatorcontrib>Gray, Samuel A.</creatorcontrib><creatorcontrib>Shubin, Yura S.</creatorcontrib><creatorcontrib>Kulagina, Nadezhda</creatorcontrib><creatorcontrib>Cuttino, David S.</creatorcontrib><creatorcontrib>Shaffer, Kara M.</creatorcontrib><creatorcontrib>Eisemann, Kevin</creatorcontrib><creatorcontrib>Curran, Anthony</creatorcontrib><creatorcontrib>Zim, Bret</creatorcontrib><creatorcontrib>Gross, Guenter W.</creatorcontrib><creatorcontrib>O'Shaughnessy, Thomas J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biosensors & bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pancrazio, Joseph J.</au><au>Gray, Samuel A.</au><au>Shubin, Yura S.</au><au>Kulagina, Nadezhda</au><au>Cuttino, David S.</au><au>Shaffer, Kara M.</au><au>Eisemann, Kevin</au><au>Curran, Anthony</au><au>Zim, Bret</au><au>Gross, Guenter W.</au><au>O'Shaughnessy, Thomas J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A portable microelectrode array recording system incorporating cultured neuronal networks for neurotoxin detection</atitle><jtitle>Biosensors & bioelectronics</jtitle><addtitle>Biosens Bioelectron</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>18</volume><issue>11</issue><spage>1339</spage><epage>1347</epage><pages>1339-1347</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Cultured neuronal networks, which have the capacity to respond to a wide range of neuroactive compounds, have been suggested to be useful for both screening known analytes and unknown compounds for acute neuropharmacologic effects. Extracellular recording from cultured neuronal networks provides a means for extracting physiologically relevant activity, i.e. action potential firing, in a noninvasive manner conducive for long-term measurements. Previous work from our laboratory described prototype portable systems capable of high signal-to-noise extracellular recordings from cardiac myocytes. The present work describes a portable system tailored to monitoring neuronal extracellular potentials that readily incorporates standardized microelectrode arrays developed by and in use at the University of North Texas. This system utilizes low noise amplifier and filter boards, a two-stage thermal control system with integrated fluidics and a graphical user interface for data acquisition and control implemented on a personal computer. Wherever possible, off-the-shelf components have been utilized for system design and fabrication. During use with cultured neuronal networks, the system typically exhibits input referred noise levels of only 4–6 μV
RMS, such that extracellular potentials exceeding 40 μV can be readily resolved. A flow rate of up to 1 ml/min was achieved while the cell recording chamber temperature was maintained within a range of 36–37
°C. To demonstrate the capability of this system to resolve small extracellular potentials, pharmacological experiments with cultured neuronal networks have been performed using ion channel blockers, tetrodotoxin and tityustoxin. The implications of the experiments for neurotoxin detection are discussed.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><pmid>12896834</pmid><doi>10.1016/S0956-5663(03)00092-7</doi><tpages>9</tpages></addata></record> |
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subjects | Action Potentials - drug effects Action Potentials - physiology Amplifier Animals Array Biological and medical sciences Biosensing Techniques - instrumentation Biosensing Techniques - methods Biosensor Biosensors Biotechnology Cell Culture Techniques - instrumentation Cell Culture Techniques - methods Cells, Cultured Dose-Response Relationship, Drug Electrophysiology - instrumentation Electrophysiology - methods Environmental Exposure - analysis Equipment Design Equipment Failure Analysis Extracellular recording Feasibility Studies Fundamental and applied biological sciences. Psychology Information Storage and Retrieval - methods ion channel blockers Methods. Procedures. Technologies Mice Mice, Inbred ICR Microelectrode array Microelectrodes Miniaturization Nerve Net - drug effects Nerve Net - physiology Neurotoxins - analysis Neurotoxins - poisoning Portable Primary neuronal cultures Reproducibility of Results Scorpion Venoms - analysis Scorpion Venoms - poisoning Sensitivity and Specificity signal-to-noise ratio tetrodotoxin Tetrodotoxin - analysis Tetrodotoxin - poisoning tityustoxin User-Computer Interface Various methods and equipments |
title | A portable microelectrode array recording system incorporating cultured neuronal networks for neurotoxin detection |
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