Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction
A microfluidic system that allowed us to perform the real-time polymerase chain reaction (PCR) in a glass-silicon microchip containing nine 250-nL microreactors was developed and studied. The resulting high heating/cooling rates of a PCR mixture in a microreactor allowed us to optimize the amplifica...
Gespeichert in:
Veröffentlicht in: | Journal of analytical chemistry (New York, N.Y.) N.Y.), 2008-02, Vol.63 (2), p.192-198 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 198 |
---|---|
container_issue | 2 |
container_start_page | 192 |
container_title | Journal of analytical chemistry (New York, N.Y.) |
container_volume | 63 |
creator | Slyadnev, M N Lavrova, M V Erkin, MA Kazakov, V A Ganeev, A A |
description | A microfluidic system that allowed us to perform the real-time polymerase chain reaction (PCR) in a glass-silicon microchip containing nine 250-nL microreactors was developed and studied. The resulting high heating/cooling rates of a PCR mixture in a microreactor allowed us to optimize the amplification mode (1 min/cycle). The silicon surface of microreactors was successfully passivated. The resulting analytical system allowed us to measure the PCR kinetic curves in chip microreactors at a DNA concentration of similar to 5 x 10 super(4) copies per microreactor. It was found that, if the PCR is performed in a microchip with real-time detection using the optimized amplification mode, the result can be obtained 13-14 min after the onset of reaction. |
doi_str_mv | 10.1007/s10809-008-2015-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_19693356</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19693356</sourcerecordid><originalsourceid>FETCH-LOGICAL-p101t-a5cfe1857d3c9cc90fc283f0e211772d0ca7ec9abbebec06d52cce54748caeaa3</originalsourceid><addsrcrecordid>eNotjMlOwzAURS0EEqXwAey8Ymd4jpvBy6plkirYwLpyX56pkR2H2EH07wnD6g7SOYxdSriWAPVNktCAFgCNKECWojhiM1lNS0mtj6cOlRRaLZpTdpbSOwDoRlYz9rWmT_KxD9RlHi03PIw-u4EM5jjw4HCI1o-udcjTIWUK3E5_3hNvKdMQXGeyi90Pu35a8jG57o1PuBfZBeJ99IdAg0nEcW9cx3_NE3DOTqzxiS7-c85e725fVg9i83z_uFpuRC9BZmFKtCSbsm4VakQNFotGWaBCyrouWkBTE2qz29GOEKq2LBCpXNSLBg0Zo-bs6s_bD_FjpJS3wSUk701HcUxbqSutVFmpbxLjZBQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19693356</pqid></control><display><type>article</type><title>Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction</title><source>SpringerLink</source><creator>Slyadnev, M N ; Lavrova, M V ; Erkin, MA ; Kazakov, V A ; Ganeev, A A</creator><creatorcontrib>Slyadnev, M N ; Lavrova, M V ; Erkin, MA ; Kazakov, V A ; Ganeev, A A</creatorcontrib><description>A microfluidic system that allowed us to perform the real-time polymerase chain reaction (PCR) in a glass-silicon microchip containing nine 250-nL microreactors was developed and studied. The resulting high heating/cooling rates of a PCR mixture in a microreactor allowed us to optimize the amplification mode (1 min/cycle). The silicon surface of microreactors was successfully passivated. The resulting analytical system allowed us to measure the PCR kinetic curves in chip microreactors at a DNA concentration of similar to 5 x 10 super(4) copies per microreactor. It was found that, if the PCR is performed in a microchip with real-time detection using the optimized amplification mode, the result can be obtained 13-14 min after the onset of reaction.</description><identifier>ISSN: 1061-9348</identifier><identifier>EISSN: 1608-3199</identifier><identifier>DOI: 10.1007/s10809-008-2015-2</identifier><language>eng</language><ispartof>Journal of analytical chemistry (New York, N.Y.), 2008-02, Vol.63 (2), p.192-198</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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Slyadnev, M N</creatorcontrib><creatorcontrib>Lavrova, M V</creatorcontrib><creatorcontrib>Erkin, MA</creatorcontrib><creatorcontrib>Kazakov, V A</creatorcontrib><creatorcontrib>Ganeev, A A</creatorcontrib><title>Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction</title><title>Journal of analytical chemistry (New York, N.Y.)</title><description>A microfluidic system that allowed us to perform the real-time polymerase chain reaction (PCR) in a glass-silicon microchip containing nine 250-nL microreactors was developed and studied. The resulting high heating/cooling rates of a PCR mixture in a microreactor allowed us to optimize the amplification mode (1 min/cycle). The silicon surface of microreactors was successfully passivated. The resulting analytical system allowed us to measure the PCR kinetic curves in chip microreactors at a DNA concentration of similar to 5 x 10 super(4) copies per microreactor. It was found that, if the PCR is performed in a microchip with real-time detection using the optimized amplification mode, the result can be obtained 13-14 min after the onset of reaction.</description><issn>1061-9348</issn><issn>1608-3199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNotjMlOwzAURS0EEqXwAey8Ymd4jpvBy6plkirYwLpyX56pkR2H2EH07wnD6g7SOYxdSriWAPVNktCAFgCNKECWojhiM1lNS0mtj6cOlRRaLZpTdpbSOwDoRlYz9rWmT_KxD9RlHi03PIw-u4EM5jjw4HCI1o-udcjTIWUK3E5_3hNvKdMQXGeyi90Pu35a8jG57o1PuBfZBeJ99IdAg0nEcW9cx3_NE3DOTqzxiS7-c85e725fVg9i83z_uFpuRC9BZmFKtCSbsm4VakQNFotGWaBCyrouWkBTE2qz29GOEKq2LBCpXNSLBg0Zo-bs6s_bD_FjpJS3wSUk701HcUxbqSutVFmpbxLjZBQ</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Slyadnev, M N</creator><creator>Lavrova, M V</creator><creator>Erkin, MA</creator><creator>Kazakov, V A</creator><creator>Ganeev, A A</creator><scope>7TM</scope></search><sort><creationdate>20080201</creationdate><title>Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction</title><author>Slyadnev, M N ; Lavrova, M V ; Erkin, MA ; Kazakov, V A ; Ganeev, A A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p101t-a5cfe1857d3c9cc90fc283f0e211772d0ca7ec9abbebec06d52cce54748caeaa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Slyadnev, M N</creatorcontrib><creatorcontrib>Lavrova, M V</creatorcontrib><creatorcontrib>Erkin, MA</creatorcontrib><creatorcontrib>Kazakov, V A</creatorcontrib><creatorcontrib>Ganeev, A A</creatorcontrib><collection>Nucleic Acids Abstracts</collection><jtitle>Journal of analytical chemistry (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Slyadnev, M N</au><au>Lavrova, M V</au><au>Erkin, MA</au><au>Kazakov, V A</au><au>Ganeev, A A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction</atitle><jtitle>Journal of analytical chemistry (New York, N.Y.)</jtitle><date>2008-02-01</date><risdate>2008</risdate><volume>63</volume><issue>2</issue><spage>192</spage><epage>198</epage><pages>192-198</pages><issn>1061-9348</issn><eissn>1608-3199</eissn><abstract>A microfluidic system that allowed us to perform the real-time polymerase chain reaction (PCR) in a glass-silicon microchip containing nine 250-nL microreactors was developed and studied. The resulting high heating/cooling rates of a PCR mixture in a microreactor allowed us to optimize the amplification mode (1 min/cycle). The silicon surface of microreactors was successfully passivated. The resulting analytical system allowed us to measure the PCR kinetic curves in chip microreactors at a DNA concentration of similar to 5 x 10 super(4) copies per microreactor. It was found that, if the PCR is performed in a microchip with real-time detection using the optimized amplification mode, the result can be obtained 13-14 min after the onset of reaction.</abstract><doi>10.1007/s10809-008-2015-2</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1061-9348 |
ispartof | Journal of analytical chemistry (New York, N.Y.), 2008-02, Vol.63 (2), p.192-198 |
issn | 1061-9348 1608-3199 |
language | eng |
recordid | cdi_proquest_miscellaneous_19693356 |
source | SpringerLink |
title | Development of a multireactor microfluidic system for the determination of DNA using real-time polymerase chain reaction |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T15%3A14%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20a%20multireactor%20microfluidic%20system%20for%20the%20determination%20of%20DNA%20using%20real-time%20polymerase%20chain%20reaction&rft.jtitle=Journal%20of%20analytical%20chemistry%20(New%20York,%20N.Y.)&rft.au=Slyadnev,%20M%20N&rft.date=2008-02-01&rft.volume=63&rft.issue=2&rft.spage=192&rft.epage=198&rft.pages=192-198&rft.issn=1061-9348&rft.eissn=1608-3199&rft_id=info:doi/10.1007/s10809-008-2015-2&rft_dat=%3Cproquest%3E19693356%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19693356&rft_id=info:pmid/&rfr_iscdi=true |