A simple device using magnetic transportation for droplet-based PCR
The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hyd...
Gespeichert in:
Veröffentlicht in: | Biomedical microdevices 2007-10, Vol.9 (5), p.695-702 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 702 |
---|---|
container_issue | 5 |
container_start_page | 695 |
container_title | Biomedical microdevices |
container_volume | 9 |
creator | Ohashi, Tetsuo Kuyama, Hiroki Hanafusa, Nobuhiro Togawa, Yoshiyuki |
description | The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hydrophilic magnetic beads in a flat-bottomed, tray-type reactor filled with silicone oil. The whole droplets sink to the bottom of the reactor because their specific gravity is greater than that of the silicone oil used here. The droplets follow the movement of a magnet located underneath the reactor. The notable advantage of the droplet-based PCR is the ability to switch rapidly the proposed reaction temperature by moving the droplets to the required temperature zones in the temperature gradient. The droplet-based reciprocative thermal cycling was performed by moving the droplets composed of PCR reaction mixture to the designated temperature zones on a linear temperature gradient from 50 degrees C to 94 degrees C generated on the flat bottom plate of the tray reactor. Using human-derived DNA containing the mitochondria genes as the amplification targets, the droplet-based PCR with magnetic reciprocative thermal cycling successfully provided the five PCR products ranging from 126 to 1,219 bp in 11 min with 30 cycles. More remarkably, the human genomic gene amplification targeting glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was accomplished rapidly in 3.6 min with 40 cycles. |
doi_str_mv | 10.1007/s10544-007-9078-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_743623293</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>743623293</sourcerecordid><originalsourceid>FETCH-LOGICAL-p229t-17a27def8685445574fa2022a863763c3b09c3b894a879515b474cbcf1c8d2ee3</originalsourceid><addsrcrecordid>eNqF0EtLxDAQB_AgiruufgAvEjzoKZrJO8el-IIFRfRc0jZdumwfJq2w396A68WDXmb-hx_DzCB0DvQGKNW3EagUgqRILNWG7A7QHKRmxGgDhylzowkDrWboJMYNpWCVUsdoBlpSaYyYo2yJY9MOW48r_9mUHk-x6da4devOj02Jx-C6OPRhdGPTd7juA65Cn_xIChd9hV-y11N0VLtt9Gf7vkDv93dv2SNZPT88ZcsVGRizIwHtmK58bZRJW0upRe0YZcwZxbXiJS-oTcVY4Yy2EmQhtCiLsobSVMx7vkDX33OH0H9MPo5528TSb7eu8_0Ucy24YpxZnuTVn1IZsNRY9i9klAtQQBO8_AU3_RS6dG7OgIFQ0pqELvZoKlpf5UNoWhd2-c-7-ReHFn_E</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>212146598</pqid></control><display><type>article</type><title>A simple device using magnetic transportation for droplet-based PCR</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Ohashi, Tetsuo ; Kuyama, Hiroki ; Hanafusa, Nobuhiro ; Togawa, Yoshiyuki</creator><creatorcontrib>Ohashi, Tetsuo ; Kuyama, Hiroki ; Hanafusa, Nobuhiro ; Togawa, Yoshiyuki</creatorcontrib><description>The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hydrophilic magnetic beads in a flat-bottomed, tray-type reactor filled with silicone oil. The whole droplets sink to the bottom of the reactor because their specific gravity is greater than that of the silicone oil used here. The droplets follow the movement of a magnet located underneath the reactor. The notable advantage of the droplet-based PCR is the ability to switch rapidly the proposed reaction temperature by moving the droplets to the required temperature zones in the temperature gradient. The droplet-based reciprocative thermal cycling was performed by moving the droplets composed of PCR reaction mixture to the designated temperature zones on a linear temperature gradient from 50 degrees C to 94 degrees C generated on the flat bottom plate of the tray reactor. Using human-derived DNA containing the mitochondria genes as the amplification targets, the droplet-based PCR with magnetic reciprocative thermal cycling successfully provided the five PCR products ranging from 126 to 1,219 bp in 11 min with 30 cycles. More remarkably, the human genomic gene amplification targeting glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was accomplished rapidly in 3.6 min with 40 cycles.</description><identifier>ISSN: 1387-2176</identifier><identifier>EISSN: 1572-8781</identifier><identifier>DOI: 10.1007/s10544-007-9078-y</identifier><identifier>PMID: 17505884</identifier><identifier>CODEN: BMICFC</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Base Pairing ; Chemical reactors ; DNA - genetics ; DNA, Mitochondrial - genetics ; Equipment Design ; Genes ; Glyceraldehyde-3-Phosphate Dehydrogenases - genetics ; Humans ; Magnetics ; Magnetism ; Microfluidic Analytical Techniques - instrumentation ; Microfluidic Analytical Techniques - methods ; Polymerase Chain Reaction - instrumentation ; Polymerase Chain Reaction - methods ; Proteins ; Scientific apparatus & instruments ; Temperature ; Time Factors</subject><ispartof>Biomedical microdevices, 2007-10, Vol.9 (5), p.695-702</ispartof><rights>Springer Science+Business Media, LLC 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17505884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohashi, Tetsuo</creatorcontrib><creatorcontrib>Kuyama, Hiroki</creatorcontrib><creatorcontrib>Hanafusa, Nobuhiro</creatorcontrib><creatorcontrib>Togawa, Yoshiyuki</creatorcontrib><title>A simple device using magnetic transportation for droplet-based PCR</title><title>Biomedical microdevices</title><addtitle>Biomed Microdevices</addtitle><description>The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hydrophilic magnetic beads in a flat-bottomed, tray-type reactor filled with silicone oil. The whole droplets sink to the bottom of the reactor because their specific gravity is greater than that of the silicone oil used here. The droplets follow the movement of a magnet located underneath the reactor. The notable advantage of the droplet-based PCR is the ability to switch rapidly the proposed reaction temperature by moving the droplets to the required temperature zones in the temperature gradient. The droplet-based reciprocative thermal cycling was performed by moving the droplets composed of PCR reaction mixture to the designated temperature zones on a linear temperature gradient from 50 degrees C to 94 degrees C generated on the flat bottom plate of the tray reactor. Using human-derived DNA containing the mitochondria genes as the amplification targets, the droplet-based PCR with magnetic reciprocative thermal cycling successfully provided the five PCR products ranging from 126 to 1,219 bp in 11 min with 30 cycles. More remarkably, the human genomic gene amplification targeting glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was accomplished rapidly in 3.6 min with 40 cycles.</description><subject>Base Pairing</subject><subject>Chemical reactors</subject><subject>DNA - genetics</subject><subject>DNA, Mitochondrial - genetics</subject><subject>Equipment Design</subject><subject>Genes</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</subject><subject>Humans</subject><subject>Magnetics</subject><subject>Magnetism</subject><subject>Microfluidic Analytical Techniques - instrumentation</subject><subject>Microfluidic Analytical Techniques - methods</subject><subject>Polymerase Chain Reaction - instrumentation</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Proteins</subject><subject>Scientific apparatus & instruments</subject><subject>Temperature</subject><subject>Time Factors</subject><issn>1387-2176</issn><issn>1572-8781</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0EtLxDAQB_AgiruufgAvEjzoKZrJO8el-IIFRfRc0jZdumwfJq2w396A68WDXmb-hx_DzCB0DvQGKNW3EagUgqRILNWG7A7QHKRmxGgDhylzowkDrWboJMYNpWCVUsdoBlpSaYyYo2yJY9MOW48r_9mUHk-x6da4devOj02Jx-C6OPRhdGPTd7juA65Cn_xIChd9hV-y11N0VLtt9Gf7vkDv93dv2SNZPT88ZcsVGRizIwHtmK58bZRJW0upRe0YZcwZxbXiJS-oTcVY4Yy2EmQhtCiLsobSVMx7vkDX33OH0H9MPo5528TSb7eu8_0Ucy24YpxZnuTVn1IZsNRY9i9klAtQQBO8_AU3_RS6dG7OgIFQ0pqELvZoKlpf5UNoWhd2-c-7-ReHFn_E</recordid><startdate>200710</startdate><enddate>200710</enddate><creator>Ohashi, Tetsuo</creator><creator>Kuyama, Hiroki</creator><creator>Hanafusa, Nobuhiro</creator><creator>Togawa, Yoshiyuki</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7SP</scope><scope>7TB</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200710</creationdate><title>A simple device using magnetic transportation for droplet-based PCR</title><author>Ohashi, Tetsuo ; Kuyama, Hiroki ; Hanafusa, Nobuhiro ; Togawa, Yoshiyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p229t-17a27def8685445574fa2022a863763c3b09c3b894a879515b474cbcf1c8d2ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Base Pairing</topic><topic>Chemical reactors</topic><topic>DNA - genetics</topic><topic>DNA, Mitochondrial - genetics</topic><topic>Equipment Design</topic><topic>Genes</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</topic><topic>Humans</topic><topic>Magnetics</topic><topic>Magnetism</topic><topic>Microfluidic Analytical Techniques - instrumentation</topic><topic>Microfluidic Analytical Techniques - methods</topic><topic>Polymerase Chain Reaction - instrumentation</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Proteins</topic><topic>Scientific apparatus & instruments</topic><topic>Temperature</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohashi, Tetsuo</creatorcontrib><creatorcontrib>Kuyama, Hiroki</creatorcontrib><creatorcontrib>Hanafusa, Nobuhiro</creatorcontrib><creatorcontrib>Togawa, Yoshiyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical microdevices</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohashi, Tetsuo</au><au>Kuyama, Hiroki</au><au>Hanafusa, Nobuhiro</au><au>Togawa, Yoshiyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple device using magnetic transportation for droplet-based PCR</atitle><jtitle>Biomedical microdevices</jtitle><addtitle>Biomed Microdevices</addtitle><date>2007-10</date><risdate>2007</risdate><volume>9</volume><issue>5</issue><spage>695</spage><epage>702</epage><pages>695-702</pages><issn>1387-2176</issn><eissn>1572-8781</eissn><coden>BMICFC</coden><abstract>The Polymerase chain reaction (PCR) was successfully and rapidly performed in a simple reaction device devoid of channels, pumps, valves, or other control elements used in conventional lab-on-a-chip technology. The basic concept of this device is the transportation of aqueous droplets containing hydrophilic magnetic beads in a flat-bottomed, tray-type reactor filled with silicone oil. The whole droplets sink to the bottom of the reactor because their specific gravity is greater than that of the silicone oil used here. The droplets follow the movement of a magnet located underneath the reactor. The notable advantage of the droplet-based PCR is the ability to switch rapidly the proposed reaction temperature by moving the droplets to the required temperature zones in the temperature gradient. The droplet-based reciprocative thermal cycling was performed by moving the droplets composed of PCR reaction mixture to the designated temperature zones on a linear temperature gradient from 50 degrees C to 94 degrees C generated on the flat bottom plate of the tray reactor. Using human-derived DNA containing the mitochondria genes as the amplification targets, the droplet-based PCR with magnetic reciprocative thermal cycling successfully provided the five PCR products ranging from 126 to 1,219 bp in 11 min with 30 cycles. More remarkably, the human genomic gene amplification targeting glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was accomplished rapidly in 3.6 min with 40 cycles.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>17505884</pmid><doi>10.1007/s10544-007-9078-y</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1387-2176 |
ispartof | Biomedical microdevices, 2007-10, Vol.9 (5), p.695-702 |
issn | 1387-2176 1572-8781 |
language | eng |
recordid | cdi_proquest_miscellaneous_743623293 |
source | MEDLINE; SpringerLink Journals |
subjects | Base Pairing Chemical reactors DNA - genetics DNA, Mitochondrial - genetics Equipment Design Genes Glyceraldehyde-3-Phosphate Dehydrogenases - genetics Humans Magnetics Magnetism Microfluidic Analytical Techniques - instrumentation Microfluidic Analytical Techniques - methods Polymerase Chain Reaction - instrumentation Polymerase Chain Reaction - methods Proteins Scientific apparatus & instruments Temperature Time Factors |
title | A simple device using magnetic transportation for droplet-based PCR |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T05%3A50%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20simple%20device%20using%20magnetic%20transportation%20for%20droplet-based%20PCR&rft.jtitle=Biomedical%20microdevices&rft.au=Ohashi,%20Tetsuo&rft.date=2007-10&rft.volume=9&rft.issue=5&rft.spage=695&rft.epage=702&rft.pages=695-702&rft.issn=1387-2176&rft.eissn=1572-8781&rft.coden=BMICFC&rft_id=info:doi/10.1007/s10544-007-9078-y&rft_dat=%3Cproquest_pubme%3E743623293%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=212146598&rft_id=info:pmid/17505884&rfr_iscdi=true |