Digital PCR on an integrated self-priming compartmentalization chip

An integrated on-chip valve-free and power-free microfluidic digital PCR device is for the first time developed by making use of a novel self-priming compartmentalization and simple dehydration control to realize 'divide and conquer' for single DNA molecule detection. The high gas solubili...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Lab on a chip 2014-03, Vol.14 (6), p.1176-1185
Hauptverfasser: Zhu, Qiangyuan, Qiu, Lin, Yu, Bingwen, Xu, Yanan, Gao, Yibo, Pan, Tingting, Tian, Qingchang, Song, Qi, Jin, Wei, Jin, Qinhan, Mu, Ying
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1185
container_issue 6
container_start_page 1176
container_title Lab on a chip
container_volume 14
creator Zhu, Qiangyuan
Qiu, Lin
Yu, Bingwen
Xu, Yanan
Gao, Yibo
Pan, Tingting
Tian, Qingchang
Song, Qi
Jin, Wei
Jin, Qinhan
Mu, Ying
description An integrated on-chip valve-free and power-free microfluidic digital PCR device is for the first time developed by making use of a novel self-priming compartmentalization and simple dehydration control to realize 'divide and conquer' for single DNA molecule detection. The high gas solubility of PDMS is exploited to provide the built-in power of self-priming so that the sample and oil are sequentially sucked into the device to realize sample self-compartmentalization based on surface tension. The lifespan of its self-priming capability was about two weeks tested using an air-tight packaging bottle sealed with a small amount of petroleum jelly, which is significant for a practical platform. The SPC chip contains 5120 independent 5 nL microchambers, allowing the samples to be compartmentalized completely. Using this platform, three different abundances of lung cancer related genes are detected to demonstrate the feasibility and flexibility of the microchip for amplifying a single nucleic acid molecule. For maximal accuracy, within less than 5% of the measurement deviation, the optimal number of positive chambers is between 400 and 1250 evaluated by the Poisson distribution, which means one panel can detect an average of 480 to 4804 template molecules. This device without world-to-chip connections eliminates the constraint of the complex pipeline control, and is an integrated on-chip platform, which would be a significant improvement to digital PCR automation and more user-friendly.
doi_str_mv 10.1039/c3lc51327k
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1671486018</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1499152430</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-7b30f4045824e90bdbdf942c14e97c9ac466e4c06b0f5cd8ac8b288f99ae1ec13</originalsourceid><addsrcrecordid>eNqF0E1LxDAQBuAgiruuXvwB0qMI1UyTpslR6icuKKLnkqbTNdovk-xBf71dd92rp5mBhxfmJeQY6DlQpi4Ma0wKLMk-dsgUeMZiClLtbneVTciB9--UQsqF3CeThHMJlIspya_swgbdRE_5c9R3ke4i2wVcOB2wijw2dTw429puEZm-HbQLLXajt9862NGbNzsckr1aNx6PNnNGXm-uX_K7eP54e59fzmPDpAhxVjJac8pTmXBUtKzKqlY8MTBemVHacCGQGypKWqemktrIMpGyVkojoAE2I6fr3MH1n0v0oWitN9g0usN-6QsQGXApxuf_p1wpSBPO6EjP1tS43nuHdbF6WLuvAmix6rfI2Tz_7fdhxCeb3GXZYrWlf4WyH87sdRk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1499152430</pqid></control><display><type>article</type><title>Digital PCR on an integrated self-priming compartmentalization chip</title><source>MEDLINE</source><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Zhu, Qiangyuan ; Qiu, Lin ; Yu, Bingwen ; Xu, Yanan ; Gao, Yibo ; Pan, Tingting ; Tian, Qingchang ; Song, Qi ; Jin, Wei ; Jin, Qinhan ; Mu, Ying</creator><creatorcontrib>Zhu, Qiangyuan ; Qiu, Lin ; Yu, Bingwen ; Xu, Yanan ; Gao, Yibo ; Pan, Tingting ; Tian, Qingchang ; Song, Qi ; Jin, Wei ; Jin, Qinhan ; Mu, Ying</creatorcontrib><description>An integrated on-chip valve-free and power-free microfluidic digital PCR device is for the first time developed by making use of a novel self-priming compartmentalization and simple dehydration control to realize 'divide and conquer' for single DNA molecule detection. The high gas solubility of PDMS is exploited to provide the built-in power of self-priming so that the sample and oil are sequentially sucked into the device to realize sample self-compartmentalization based on surface tension. The lifespan of its self-priming capability was about two weeks tested using an air-tight packaging bottle sealed with a small amount of petroleum jelly, which is significant for a practical platform. The SPC chip contains 5120 independent 5 nL microchambers, allowing the samples to be compartmentalized completely. Using this platform, three different abundances of lung cancer related genes are detected to demonstrate the feasibility and flexibility of the microchip for amplifying a single nucleic acid molecule. For maximal accuracy, within less than 5% of the measurement deviation, the optimal number of positive chambers is between 400 and 1250 evaluated by the Poisson distribution, which means one panel can detect an average of 480 to 4804 template molecules. This device without world-to-chip connections eliminates the constraint of the complex pipeline control, and is an integrated on-chip platform, which would be a significant improvement to digital PCR automation and more user-friendly.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/c3lc51327k</identifier><identifier>PMID: 24481046</identifier><language>eng</language><publisher>England</publisher><subject>Automation ; Cell Line, Tumor ; Chips ; Deviation ; Devices ; Digital ; DNA, Neoplasm - chemistry ; Gas solubility ; Humans ; Microfluidic Analytical Techniques - instrumentation ; Microfluidic Analytical Techniques - methods ; Panels ; Platforms ; Polymerase Chain Reaction - instrumentation ; Polymerase Chain Reaction - methods</subject><ispartof>Lab on a chip, 2014-03, Vol.14 (6), p.1176-1185</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-7b30f4045824e90bdbdf942c14e97c9ac466e4c06b0f5cd8ac8b288f99ae1ec13</citedby><cites>FETCH-LOGICAL-c386t-7b30f4045824e90bdbdf942c14e97c9ac466e4c06b0f5cd8ac8b288f99ae1ec13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24481046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Qiangyuan</creatorcontrib><creatorcontrib>Qiu, Lin</creatorcontrib><creatorcontrib>Yu, Bingwen</creatorcontrib><creatorcontrib>Xu, Yanan</creatorcontrib><creatorcontrib>Gao, Yibo</creatorcontrib><creatorcontrib>Pan, Tingting</creatorcontrib><creatorcontrib>Tian, Qingchang</creatorcontrib><creatorcontrib>Song, Qi</creatorcontrib><creatorcontrib>Jin, Wei</creatorcontrib><creatorcontrib>Jin, Qinhan</creatorcontrib><creatorcontrib>Mu, Ying</creatorcontrib><title>Digital PCR on an integrated self-priming compartmentalization chip</title><title>Lab on a chip</title><addtitle>Lab Chip</addtitle><description>An integrated on-chip valve-free and power-free microfluidic digital PCR device is for the first time developed by making use of a novel self-priming compartmentalization and simple dehydration control to realize 'divide and conquer' for single DNA molecule detection. The high gas solubility of PDMS is exploited to provide the built-in power of self-priming so that the sample and oil are sequentially sucked into the device to realize sample self-compartmentalization based on surface tension. The lifespan of its self-priming capability was about two weeks tested using an air-tight packaging bottle sealed with a small amount of petroleum jelly, which is significant for a practical platform. The SPC chip contains 5120 independent 5 nL microchambers, allowing the samples to be compartmentalized completely. Using this platform, three different abundances of lung cancer related genes are detected to demonstrate the feasibility and flexibility of the microchip for amplifying a single nucleic acid molecule. For maximal accuracy, within less than 5% of the measurement deviation, the optimal number of positive chambers is between 400 and 1250 evaluated by the Poisson distribution, which means one panel can detect an average of 480 to 4804 template molecules. This device without world-to-chip connections eliminates the constraint of the complex pipeline control, and is an integrated on-chip platform, which would be a significant improvement to digital PCR automation and more user-friendly.</description><subject>Automation</subject><subject>Cell Line, Tumor</subject><subject>Chips</subject><subject>Deviation</subject><subject>Devices</subject><subject>Digital</subject><subject>DNA, Neoplasm - chemistry</subject><subject>Gas solubility</subject><subject>Humans</subject><subject>Microfluidic Analytical Techniques - instrumentation</subject><subject>Microfluidic Analytical Techniques - methods</subject><subject>Panels</subject><subject>Platforms</subject><subject>Polymerase Chain Reaction - instrumentation</subject><subject>Polymerase Chain Reaction - methods</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1LxDAQBuAgiruuXvwB0qMI1UyTpslR6icuKKLnkqbTNdovk-xBf71dd92rp5mBhxfmJeQY6DlQpi4Ma0wKLMk-dsgUeMZiClLtbneVTciB9--UQsqF3CeThHMJlIspya_swgbdRE_5c9R3ke4i2wVcOB2wijw2dTw429puEZm-HbQLLXajt9862NGbNzsckr1aNx6PNnNGXm-uX_K7eP54e59fzmPDpAhxVjJac8pTmXBUtKzKqlY8MTBemVHacCGQGypKWqemktrIMpGyVkojoAE2I6fr3MH1n0v0oWitN9g0usN-6QsQGXApxuf_p1wpSBPO6EjP1tS43nuHdbF6WLuvAmix6rfI2Tz_7fdhxCeb3GXZYrWlf4WyH87sdRk</recordid><startdate>20140321</startdate><enddate>20140321</enddate><creator>Zhu, Qiangyuan</creator><creator>Qiu, Lin</creator><creator>Yu, Bingwen</creator><creator>Xu, Yanan</creator><creator>Gao, Yibo</creator><creator>Pan, Tingting</creator><creator>Tian, Qingchang</creator><creator>Song, Qi</creator><creator>Jin, Wei</creator><creator>Jin, Qinhan</creator><creator>Mu, Ying</creator><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>7X8</scope><scope>7SP</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>L7M</scope></search><sort><creationdate>20140321</creationdate><title>Digital PCR on an integrated self-priming compartmentalization chip</title><author>Zhu, Qiangyuan ; Qiu, Lin ; Yu, Bingwen ; Xu, Yanan ; Gao, Yibo ; Pan, Tingting ; Tian, Qingchang ; Song, Qi ; Jin, Wei ; Jin, Qinhan ; Mu, Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-7b30f4045824e90bdbdf942c14e97c9ac466e4c06b0f5cd8ac8b288f99ae1ec13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Automation</topic><topic>Cell Line, Tumor</topic><topic>Chips</topic><topic>Deviation</topic><topic>Devices</topic><topic>Digital</topic><topic>DNA, Neoplasm - chemistry</topic><topic>Gas solubility</topic><topic>Humans</topic><topic>Microfluidic Analytical Techniques - instrumentation</topic><topic>Microfluidic Analytical Techniques - methods</topic><topic>Panels</topic><topic>Platforms</topic><topic>Polymerase Chain Reaction - instrumentation</topic><topic>Polymerase Chain Reaction - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Qiangyuan</creatorcontrib><creatorcontrib>Qiu, Lin</creatorcontrib><creatorcontrib>Yu, Bingwen</creatorcontrib><creatorcontrib>Xu, Yanan</creatorcontrib><creatorcontrib>Gao, Yibo</creatorcontrib><creatorcontrib>Pan, Tingting</creatorcontrib><creatorcontrib>Tian, Qingchang</creatorcontrib><creatorcontrib>Song, Qi</creatorcontrib><creatorcontrib>Jin, Wei</creatorcontrib><creatorcontrib>Jin, Qinhan</creatorcontrib><creatorcontrib>Mu, Ying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Qiangyuan</au><au>Qiu, Lin</au><au>Yu, Bingwen</au><au>Xu, Yanan</au><au>Gao, Yibo</au><au>Pan, Tingting</au><au>Tian, Qingchang</au><au>Song, Qi</au><au>Jin, Wei</au><au>Jin, Qinhan</au><au>Mu, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Digital PCR on an integrated self-priming compartmentalization chip</atitle><jtitle>Lab on a chip</jtitle><addtitle>Lab Chip</addtitle><date>2014-03-21</date><risdate>2014</risdate><volume>14</volume><issue>6</issue><spage>1176</spage><epage>1185</epage><pages>1176-1185</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>An integrated on-chip valve-free and power-free microfluidic digital PCR device is for the first time developed by making use of a novel self-priming compartmentalization and simple dehydration control to realize 'divide and conquer' for single DNA molecule detection. The high gas solubility of PDMS is exploited to provide the built-in power of self-priming so that the sample and oil are sequentially sucked into the device to realize sample self-compartmentalization based on surface tension. The lifespan of its self-priming capability was about two weeks tested using an air-tight packaging bottle sealed with a small amount of petroleum jelly, which is significant for a practical platform. The SPC chip contains 5120 independent 5 nL microchambers, allowing the samples to be compartmentalized completely. Using this platform, three different abundances of lung cancer related genes are detected to demonstrate the feasibility and flexibility of the microchip for amplifying a single nucleic acid molecule. For maximal accuracy, within less than 5% of the measurement deviation, the optimal number of positive chambers is between 400 and 1250 evaluated by the Poisson distribution, which means one panel can detect an average of 480 to 4804 template molecules. This device without world-to-chip connections eliminates the constraint of the complex pipeline control, and is an integrated on-chip platform, which would be a significant improvement to digital PCR automation and more user-friendly.</abstract><cop>England</cop><pmid>24481046</pmid><doi>10.1039/c3lc51327k</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1473-0197
ispartof Lab on a chip, 2014-03, Vol.14 (6), p.1176-1185
issn 1473-0197
1473-0189
language eng
recordid cdi_proquest_miscellaneous_1671486018
source MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Automation
Cell Line, Tumor
Chips
Deviation
Devices
Digital
DNA, Neoplasm - chemistry
Gas solubility
Humans
Microfluidic Analytical Techniques - instrumentation
Microfluidic Analytical Techniques - methods
Panels
Platforms
Polymerase Chain Reaction - instrumentation
Polymerase Chain Reaction - methods
title Digital PCR on an integrated self-priming compartmentalization chip
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T18%3A54%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Digital%20PCR%20on%20an%20integrated%20self-priming%20compartmentalization%20chip&rft.jtitle=Lab%20on%20a%20chip&rft.au=Zhu,%20Qiangyuan&rft.date=2014-03-21&rft.volume=14&rft.issue=6&rft.spage=1176&rft.epage=1185&rft.pages=1176-1185&rft.issn=1473-0197&rft.eissn=1473-0189&rft_id=info:doi/10.1039/c3lc51327k&rft_dat=%3Cproquest_cross%3E1499152430%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1499152430&rft_id=info:pmid/24481046&rfr_iscdi=true