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Portable Microfluidic System for Rapid Genetic Testing
SUMMARY Polymerase chain reaction (PCR) is a key technology of genetic testing, but the long thermal cycling time has been a problem in achieving rapid diagnosis of pathogenic organisms and cancer. We describe a simple, portable, and rapid genetic testing system based on ultrafast segment flow and f...
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Published in: | Electronics and communications in Japan 2015-12, Vol.98 (12), p.1-6 |
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container_issue | 12 |
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container_title | Electronics and communications in Japan |
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creator | NAGAI, HIDENORI FUCHIWAKI, YUSUKE |
description | SUMMARY
Polymerase chain reaction (PCR) is a key technology of genetic testing, but the long thermal cycling time has been a problem in achieving rapid diagnosis of pathogenic organisms and cancer. We describe a simple, portable, and rapid genetic testing system based on ultrafast segment flow and fluorescent detection. In particular, we improved the flow‐through PCR to accelerate the thermal cycling time and simplify the operation for practical use. The PCR solution was injected in a small volume of about several microliters by an air syringe, and flowed as segment flow. The segment of PCR solution was moved in a serpentine microchannel on a microfluidic device over two temperature zones for denaturation and annealing/extension reactions. The base plate formed upon the serpentine microchannel pattern was made of cyclo‐olefin polymer (COP) and covered with a thin transparent film. Furthermore, a specialized portable system was developed for the microfluidic device of a segment‐flow PCR. Heater units, a syringe pump, a fluorescence detector, and PC were integrated in a suitcase for portable use. Using this portable system, a microorganism modeling anthrax and a point mutation of FGFR3 gene were successfully detected within 6.5 min. |
doi_str_mv | 10.1002/ecj.11753 |
format | article |
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Polymerase chain reaction (PCR) is a key technology of genetic testing, but the long thermal cycling time has been a problem in achieving rapid diagnosis of pathogenic organisms and cancer. We describe a simple, portable, and rapid genetic testing system based on ultrafast segment flow and fluorescent detection. In particular, we improved the flow‐through PCR to accelerate the thermal cycling time and simplify the operation for practical use. The PCR solution was injected in a small volume of about several microliters by an air syringe, and flowed as segment flow. The segment of PCR solution was moved in a serpentine microchannel on a microfluidic device over two temperature zones for denaturation and annealing/extension reactions. The base plate formed upon the serpentine microchannel pattern was made of cyclo‐olefin polymer (COP) and covered with a thin transparent film. Furthermore, a specialized portable system was developed for the microfluidic device of a segment‐flow PCR. Heater units, a syringe pump, a fluorescence detector, and PC were integrated in a suitcase for portable use. Using this portable system, a microorganism modeling anthrax and a point mutation of FGFR3 gene were successfully detected within 6.5 min.</description><identifier>ISSN: 1942-9533</identifier><identifier>EISSN: 1942-9541</identifier><identifier>DOI: 10.1002/ecj.11753</identifier><language>eng</language><publisher>Blackwell Publishing Ltd</publisher><subject>Anthrax ; Devices ; Fluorescence ; genetic testing ; Genetics ; Microfluidics ; point of care testing (POCT) ; polymerase chain reaction (PCR) ; Portability ; Segments ; Thermal cycling</subject><ispartof>Electronics and communications in Japan, 2015-12, Vol.98 (12), p.1-6</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4063-fd55a92e11652a1704ea2f28f020838a01e828aa7445ae9274ee4fa998d145cb3</citedby><cites>FETCH-LOGICAL-c4063-fd55a92e11652a1704ea2f28f020838a01e828aa7445ae9274ee4fa998d145cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>NAGAI, HIDENORI</creatorcontrib><creatorcontrib>FUCHIWAKI, YUSUKE</creatorcontrib><title>Portable Microfluidic System for Rapid Genetic Testing</title><title>Electronics and communications in Japan</title><addtitle>Electron Comm Jpn</addtitle><description>SUMMARY
Polymerase chain reaction (PCR) is a key technology of genetic testing, but the long thermal cycling time has been a problem in achieving rapid diagnosis of pathogenic organisms and cancer. We describe a simple, portable, and rapid genetic testing system based on ultrafast segment flow and fluorescent detection. In particular, we improved the flow‐through PCR to accelerate the thermal cycling time and simplify the operation for practical use. The PCR solution was injected in a small volume of about several microliters by an air syringe, and flowed as segment flow. The segment of PCR solution was moved in a serpentine microchannel on a microfluidic device over two temperature zones for denaturation and annealing/extension reactions. The base plate formed upon the serpentine microchannel pattern was made of cyclo‐olefin polymer (COP) and covered with a thin transparent film. Furthermore, a specialized portable system was developed for the microfluidic device of a segment‐flow PCR. Heater units, a syringe pump, a fluorescence detector, and PC were integrated in a suitcase for portable use. Using this portable system, a microorganism modeling anthrax and a point mutation of FGFR3 gene were successfully detected within 6.5 min.</description><subject>Anthrax</subject><subject>Devices</subject><subject>Fluorescence</subject><subject>genetic testing</subject><subject>Genetics</subject><subject>Microfluidics</subject><subject>point of care testing (POCT)</subject><subject>polymerase chain reaction (PCR)</subject><subject>Portability</subject><subject>Segments</subject><subject>Thermal cycling</subject><issn>1942-9533</issn><issn>1942-9541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kMtOwzAQRS0EEqWw4A-yhEVaP2NnifoEteVVYGm5yRi5pE2xU0H_nkCgO1Yz0pw7ozkInRPcIRjTLmTLDiFSsAPUIimncSo4Odz3jB2jkxCWGCdccNZCyV3pK7MoIJq6zJe22LrcZdHjLlSwimzpowezcXk0gjVU9WAOoXLr11N0ZE0R4Oy3ttHTcDDvjePJ7ei6dzWJM44TFttcCJNSICQR1BCJORhqqbKYYsWUwQQUVcZIzoWBlEoOwK1JU5UTLrIFa6OLZu_Gl-_b-rZeuZBBUZg1lNugiZQKU5EmrEYvG7R-IwQPVm-8Wxm_0wTrbze6dqN_3NRst2E_XAG7_0E96N38JeIm4Woxn_uE8W86kUwK_TIb6elz_3427s_0kH0BdWtzJQ</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>NAGAI, HIDENORI</creator><creator>FUCHIWAKI, YUSUKE</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SC</scope><scope>7SP</scope><scope>8FD</scope><scope>JQ2</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope></search><sort><creationdate>201512</creationdate><title>Portable Microfluidic System for Rapid Genetic Testing</title><author>NAGAI, HIDENORI ; FUCHIWAKI, YUSUKE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4063-fd55a92e11652a1704ea2f28f020838a01e828aa7445ae9274ee4fa998d145cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Anthrax</topic><topic>Devices</topic><topic>Fluorescence</topic><topic>genetic testing</topic><topic>Genetics</topic><topic>Microfluidics</topic><topic>point of care testing (POCT)</topic><topic>polymerase chain reaction (PCR)</topic><topic>Portability</topic><topic>Segments</topic><topic>Thermal cycling</topic><toplevel>online_resources</toplevel><creatorcontrib>NAGAI, HIDENORI</creatorcontrib><creatorcontrib>FUCHIWAKI, YUSUKE</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Computer and Information Systems Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><jtitle>Electronics and communications in Japan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NAGAI, HIDENORI</au><au>FUCHIWAKI, YUSUKE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Portable Microfluidic System for Rapid Genetic Testing</atitle><jtitle>Electronics and communications in Japan</jtitle><addtitle>Electron Comm Jpn</addtitle><date>2015-12</date><risdate>2015</risdate><volume>98</volume><issue>12</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>1942-9533</issn><eissn>1942-9541</eissn><abstract>SUMMARY
Polymerase chain reaction (PCR) is a key technology of genetic testing, but the long thermal cycling time has been a problem in achieving rapid diagnosis of pathogenic organisms and cancer. We describe a simple, portable, and rapid genetic testing system based on ultrafast segment flow and fluorescent detection. In particular, we improved the flow‐through PCR to accelerate the thermal cycling time and simplify the operation for practical use. The PCR solution was injected in a small volume of about several microliters by an air syringe, and flowed as segment flow. The segment of PCR solution was moved in a serpentine microchannel on a microfluidic device over two temperature zones for denaturation and annealing/extension reactions. The base plate formed upon the serpentine microchannel pattern was made of cyclo‐olefin polymer (COP) and covered with a thin transparent film. Furthermore, a specialized portable system was developed for the microfluidic device of a segment‐flow PCR. Heater units, a syringe pump, a fluorescence detector, and PC were integrated in a suitcase for portable use. Using this portable system, a microorganism modeling anthrax and a point mutation of FGFR3 gene were successfully detected within 6.5 min.</abstract><pub>Blackwell Publishing Ltd</pub><doi>10.1002/ecj.11753</doi><tpages>6</tpages></addata></record> |
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subjects | Anthrax Devices Fluorescence genetic testing Genetics Microfluidics point of care testing (POCT) polymerase chain reaction (PCR) Portability Segments Thermal cycling |
title | Portable Microfluidic System for Rapid Genetic Testing |
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