Loading…

Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes

Release of neurotransmitters and hormones by Ca 2+ regulated exocytosis is a fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological, and endocrine disorders. Therefore, this area represents a relevant target for drug and therapeutic development, efforts th...

Full description

Saved in:
Bibliographic Details
Published in:Biosensors & bioelectronics 2011-12, Vol.34 (1), p.30-36
Main Authors: Ges, Igor A., Currie, Kevin P.M., Baudenbacher, Franz
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 36
container_issue 1
container_start_page 30
container_title Biosensors & bioelectronics
container_volume 34
creator Ges, Igor A.
Currie, Kevin P.M.
Baudenbacher, Franz
description Release of neurotransmitters and hormones by Ca 2+ regulated exocytosis is a fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological, and endocrine disorders. Therefore, this area represents a relevant target for drug and therapeutic development, efforts that will be aided by novel analytical tools and devices that provide mechanistically rich data with increased throughput. Toward this goal, we have electrochemically deposited iridium oxide (IrOx) films onto planar thin film platinum electrodes (20×300µm 2 ) and utilized these for quantitative detection of catecholamine exocytosis from adrenal chromaffin cells trapped in a microfluidic network. The IrOx electrodes show a linear response to norepinephrine in the range of 0–400µM, with a sensitivity of 23.1±0.5mA/(M·mm 2 ). The sensitivity of the IrOx electrodes does not change in the presence of ascorbic acid, a substance commonly found in biological samples. A replica molded polydimethylsiloxane (PDMS) microfluidic device with nanoliter sensing volumes was aligned and sealed to a glass substrate with the sensing electrodes. Small populations of chromaffin cells were trapped in the microfluidic sensing chamber and stimulated by rapid perfusion with high potassium (50mM) containing Tyrode’s solution at a flow rate of 1nL/s. Stimulation of the cells produced a rapid increase in current due to oxidation of the released catecholamines, with an estimated maximum concentration in the microfluidic device ~52µM. Thus, we demonstrate the utility of an integrated microfluidic network with IrOx electrodes for real-time quantitative detection of catecholamines released from small populations of cells.
doi_str_mv 10.1016/j.bios.2011.11.050
format article
fullrecord <record><control><sourceid>pubmedcentral</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3793634</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_3793634</sourcerecordid><originalsourceid>FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_37936343</originalsourceid><addsrcrecordid>eNqljE1OwzAQhS0EouXnAqzmAgl23CTNhg0q4gDdR64zaaZyPJEdV-0VODWRYMMa6UlP70efEC9K5kqq6vWUH4hjXkil8kWylDdirba1zjaFLm_FWjZllZVVpVfiIcaTlLJWjbwXq6LQzbao5Vp87RzaObAdcCRrHHQ4LwWxB-7BmiUM7MxIHgEvbK8zR4qQIvkjTM54E4ACdZRG4At1y-sH2GEE8uCNZ0czBljwgXuXlq8Fi86BTW5OAeHMLo0Yn8Rdb1zE519_FG8fu_37Zzalw4idRT8H49op0GjCtWVD7d_F09Ae-dzqutGV3uh_A74B89V3Eg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes</title><source>ScienceDirect Journals</source><creator>Ges, Igor A. ; Currie, Kevin P.M. ; Baudenbacher, Franz</creator><creatorcontrib>Ges, Igor A. ; Currie, Kevin P.M. ; Baudenbacher, Franz</creatorcontrib><description>Release of neurotransmitters and hormones by Ca 2+ regulated exocytosis is a fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological, and endocrine disorders. Therefore, this area represents a relevant target for drug and therapeutic development, efforts that will be aided by novel analytical tools and devices that provide mechanistically rich data with increased throughput. Toward this goal, we have electrochemically deposited iridium oxide (IrOx) films onto planar thin film platinum electrodes (20×300µm 2 ) and utilized these for quantitative detection of catecholamine exocytosis from adrenal chromaffin cells trapped in a microfluidic network. The IrOx electrodes show a linear response to norepinephrine in the range of 0–400µM, with a sensitivity of 23.1±0.5mA/(M·mm 2 ). The sensitivity of the IrOx electrodes does not change in the presence of ascorbic acid, a substance commonly found in biological samples. A replica molded polydimethylsiloxane (PDMS) microfluidic device with nanoliter sensing volumes was aligned and sealed to a glass substrate with the sensing electrodes. Small populations of chromaffin cells were trapped in the microfluidic sensing chamber and stimulated by rapid perfusion with high potassium (50mM) containing Tyrode’s solution at a flow rate of 1nL/s. Stimulation of the cells produced a rapid increase in current due to oxidation of the released catecholamines, with an estimated maximum concentration in the microfluidic device ~52µM. Thus, we demonstrate the utility of an integrated microfluidic network with IrOx electrodes for real-time quantitative detection of catecholamines released from small populations of cells.</description><identifier>ISSN: 0956-5663</identifier><identifier>EISSN: 1873-4235</identifier><identifier>DOI: 10.1016/j.bios.2011.11.050</identifier><identifier>PMID: 22398270</identifier><language>eng</language><ispartof>Biosensors &amp; bioelectronics, 2011-12, Vol.34 (1), p.30-36</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids></links><search><creatorcontrib>Ges, Igor A.</creatorcontrib><creatorcontrib>Currie, Kevin P.M.</creatorcontrib><creatorcontrib>Baudenbacher, Franz</creatorcontrib><title>Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes</title><title>Biosensors &amp; bioelectronics</title><description>Release of neurotransmitters and hormones by Ca 2+ regulated exocytosis is a fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological, and endocrine disorders. Therefore, this area represents a relevant target for drug and therapeutic development, efforts that will be aided by novel analytical tools and devices that provide mechanistically rich data with increased throughput. Toward this goal, we have electrochemically deposited iridium oxide (IrOx) films onto planar thin film platinum electrodes (20×300µm 2 ) and utilized these for quantitative detection of catecholamine exocytosis from adrenal chromaffin cells trapped in a microfluidic network. The IrOx electrodes show a linear response to norepinephrine in the range of 0–400µM, with a sensitivity of 23.1±0.5mA/(M·mm 2 ). The sensitivity of the IrOx electrodes does not change in the presence of ascorbic acid, a substance commonly found in biological samples. A replica molded polydimethylsiloxane (PDMS) microfluidic device with nanoliter sensing volumes was aligned and sealed to a glass substrate with the sensing electrodes. Small populations of chromaffin cells were trapped in the microfluidic sensing chamber and stimulated by rapid perfusion with high potassium (50mM) containing Tyrode’s solution at a flow rate of 1nL/s. Stimulation of the cells produced a rapid increase in current due to oxidation of the released catecholamines, with an estimated maximum concentration in the microfluidic device ~52µM. Thus, we demonstrate the utility of an integrated microfluidic network with IrOx electrodes for real-time quantitative detection of catecholamines released from small populations of cells.</description><issn>0956-5663</issn><issn>1873-4235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqljE1OwzAQhS0EouXnAqzmAgl23CTNhg0q4gDdR64zaaZyPJEdV-0VODWRYMMa6UlP70efEC9K5kqq6vWUH4hjXkil8kWylDdirba1zjaFLm_FWjZllZVVpVfiIcaTlLJWjbwXq6LQzbao5Vp87RzaObAdcCRrHHQ4LwWxB-7BmiUM7MxIHgEvbK8zR4qQIvkjTM54E4ACdZRG4At1y-sH2GEE8uCNZ0czBljwgXuXlq8Fi86BTW5OAeHMLo0Yn8Rdb1zE519_FG8fu_37Zzalw4idRT8H49op0GjCtWVD7d_F09Ae-dzqutGV3uh_A74B89V3Eg</recordid><startdate>20111222</startdate><enddate>20111222</enddate><creator>Ges, Igor A.</creator><creator>Currie, Kevin P.M.</creator><creator>Baudenbacher, Franz</creator><scope>5PM</scope></search><sort><creationdate>20111222</creationdate><title>Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes</title><author>Ges, Igor A. ; Currie, Kevin P.M. ; Baudenbacher, Franz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_37936343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ges, Igor A.</creatorcontrib><creatorcontrib>Currie, Kevin P.M.</creatorcontrib><creatorcontrib>Baudenbacher, Franz</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biosensors &amp; bioelectronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ges, Igor A.</au><au>Currie, Kevin P.M.</au><au>Baudenbacher, Franz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes</atitle><jtitle>Biosensors &amp; bioelectronics</jtitle><date>2011-12-22</date><risdate>2011</risdate><volume>34</volume><issue>1</issue><spage>30</spage><epage>36</epage><pages>30-36</pages><issn>0956-5663</issn><eissn>1873-4235</eissn><abstract>Release of neurotransmitters and hormones by Ca 2+ regulated exocytosis is a fundamental cellular/molecular process that is disrupted in a variety of psychiatric, neurological, and endocrine disorders. Therefore, this area represents a relevant target for drug and therapeutic development, efforts that will be aided by novel analytical tools and devices that provide mechanistically rich data with increased throughput. Toward this goal, we have electrochemically deposited iridium oxide (IrOx) films onto planar thin film platinum electrodes (20×300µm 2 ) and utilized these for quantitative detection of catecholamine exocytosis from adrenal chromaffin cells trapped in a microfluidic network. The IrOx electrodes show a linear response to norepinephrine in the range of 0–400µM, with a sensitivity of 23.1±0.5mA/(M·mm 2 ). The sensitivity of the IrOx electrodes does not change in the presence of ascorbic acid, a substance commonly found in biological samples. A replica molded polydimethylsiloxane (PDMS) microfluidic device with nanoliter sensing volumes was aligned and sealed to a glass substrate with the sensing electrodes. Small populations of chromaffin cells were trapped in the microfluidic sensing chamber and stimulated by rapid perfusion with high potassium (50mM) containing Tyrode’s solution at a flow rate of 1nL/s. Stimulation of the cells produced a rapid increase in current due to oxidation of the released catecholamines, with an estimated maximum concentration in the microfluidic device ~52µM. Thus, we demonstrate the utility of an integrated microfluidic network with IrOx electrodes for real-time quantitative detection of catecholamines released from small populations of cells.</abstract><pmid>22398270</pmid><doi>10.1016/j.bios.2011.11.050</doi></addata></record>
fulltext fulltext
identifier ISSN: 0956-5663
ispartof Biosensors & bioelectronics, 2011-12, Vol.34 (1), p.30-36
issn 0956-5663
1873-4235
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3793634
source ScienceDirect Journals
title Electrochemical detection of catecholamine exocytosis using planar iridium oxide electrodes in nanoliter microfluidic cell culture volumes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T08%3A38%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Electrochemical%20detection%20of%20catecholamine%20exocytosis%20using%20planar%20iridium%20oxide%20electrodes%20in%20nanoliter%20microfluidic%20cell%20culture%20volumes&rft.jtitle=Biosensors%20&%20bioelectronics&rft.au=Ges,%20Igor%20A.&rft.date=2011-12-22&rft.volume=34&rft.issue=1&rft.spage=30&rft.epage=36&rft.pages=30-36&rft.issn=0956-5663&rft.eissn=1873-4235&rft_id=info:doi/10.1016/j.bios.2011.11.050&rft_dat=%3Cpubmedcentral%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_3793634%3C/pubmedcentral%3E%3Cgrp_id%3Ecdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_37936343%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/22398270&rfr_iscdi=true