Microfabricated PCR-electrochemical device for simultaneous DNA amplification and detection
Microfabricated silicon/glass-based devices with functionalities of simultaneous polymerase chain reaction (PCR) target amplification and sequence-specific electrochemical (EC) detection have been successfully developed. The microchip-based device has a reaction chamber (volume of 8 microl) formed i...
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Veröffentlicht in: | Lab on a chip 2003-01, Vol.3 (2), p.100-105 |
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creator | Lee, Thomas Ming-Hung Carles, Maria C Hsing, I-Ming |
description | Microfabricated silicon/glass-based devices with functionalities of simultaneous polymerase chain reaction (PCR) target amplification and sequence-specific electrochemical (EC) detection have been successfully developed. The microchip-based device has a reaction chamber (volume of 8 microl) formed in a silicon substrate sealed by bonding to a glass substrate. Electrode materials such as gold and indium tin oxide (ITO) were patterned on the glass substrate and served as EC detection platforms where DNA probes were immobilized. Platinum temperature sensors and heaters were patterned on top of the silicon substrate for real-time, precise and rapid thermal cycling of the reaction chamber as well as for efficient target amplification by PCR. DNA analyses in the integrated PCR-EC microchip start with the asymmetric PCR amplification to produce single-stranded target amplicons, followed by immediate sequence-specific recognition of the PCR product as they hybridize to the probe-modified electrode. Two electrochemistry-based detection techniques including metal complex intercalators and nanogold particles are employed in the microdevice to achieve a sensitive detection of target DNA analytes. With the integrated PCR-EC microdevice, the detection of trace amounts of target DNA (as few as several hundred copies) is demonstrated. The ability to perform DNA amplification and EC sequence-specific product detection simultaneously in a single reaction chamber is a great leap towards the realization of a truly portable and integrated DNA analysis system. |
doi_str_mv | 10.1039/b300799e |
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The microchip-based device has a reaction chamber (volume of 8 microl) formed in a silicon substrate sealed by bonding to a glass substrate. Electrode materials such as gold and indium tin oxide (ITO) were patterned on the glass substrate and served as EC detection platforms where DNA probes were immobilized. Platinum temperature sensors and heaters were patterned on top of the silicon substrate for real-time, precise and rapid thermal cycling of the reaction chamber as well as for efficient target amplification by PCR. DNA analyses in the integrated PCR-EC microchip start with the asymmetric PCR amplification to produce single-stranded target amplicons, followed by immediate sequence-specific recognition of the PCR product as they hybridize to the probe-modified electrode. Two electrochemistry-based detection techniques including metal complex intercalators and nanogold particles are employed in the microdevice to achieve a sensitive detection of target DNA analytes. With the integrated PCR-EC microdevice, the detection of trace amounts of target DNA (as few as several hundred copies) is demonstrated. The ability to perform DNA amplification and EC sequence-specific product detection simultaneously in a single reaction chamber is a great leap towards the realization of a truly portable and integrated DNA analysis system.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/b300799e</identifier><identifier>PMID: 15100790</identifier><language>eng</language><publisher>England</publisher><subject>Electrochemistry - instrumentation ; Electrochemistry - methods ; Glass - chemistry ; Nanotechnology ; Nucleic Acid Amplification Techniques - instrumentation ; Nucleic Acid Amplification Techniques - methods ; Nucleic Acid Hybridization ; Oligonucleotide Probes - chemistry ; Polymerase Chain Reaction - instrumentation ; Polymerase Chain Reaction - methods ; Silicon - chemistry</subject><ispartof>Lab on a chip, 2003-01, Vol.3 (2), p.100-105</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-4352b75a291f80b37ad384222ded6529d494af641921d9b5b9b512d7ceab23f83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2818,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15100790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Thomas Ming-Hung</creatorcontrib><creatorcontrib>Carles, Maria C</creatorcontrib><creatorcontrib>Hsing, I-Ming</creatorcontrib><title>Microfabricated PCR-electrochemical device for simultaneous DNA amplification and detection</title><title>Lab on a chip</title><addtitle>Lab Chip</addtitle><description>Microfabricated silicon/glass-based devices with functionalities of simultaneous polymerase chain reaction (PCR) target amplification and sequence-specific electrochemical (EC) detection have been successfully developed. 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With the integrated PCR-EC microdevice, the detection of trace amounts of target DNA (as few as several hundred copies) is demonstrated. The ability to perform DNA amplification and EC sequence-specific product detection simultaneously in a single reaction chamber is a great leap towards the realization of a truly portable and integrated DNA analysis system.</description><subject>Electrochemistry - instrumentation</subject><subject>Electrochemistry - methods</subject><subject>Glass - chemistry</subject><subject>Nanotechnology</subject><subject>Nucleic Acid Amplification Techniques - instrumentation</subject><subject>Nucleic Acid Amplification Techniques - methods</subject><subject>Nucleic Acid Hybridization</subject><subject>Oligonucleotide Probes - chemistry</subject><subject>Polymerase Chain Reaction - instrumentation</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Silicon - chemistry</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLxDAQx4Mo7roKfgLpSbxU82ib5risT1gfiJ48lDwmGEm3NWkFv71ZdtXDMA9-_2Hmj9AxwecEM3GhGMZcCNhBU1JwlmNSi92_WvAJOojxA2NSFlW9jyakJGsBnqK3e6dDZ6UKTssBTPa0eM7Bgx5Cp9-hTVOfGfhyGjLbhSy6dvSDXEE3xuzyYZ7JtvfOrsWuW2VyZRI9JHnqDtGelT7C0TbP0Ov11cviNl8-3twt5stcMyGGvGAlVbyUVBBbY8W4NKwuKKUGTFVSYQpRSFsVRFBihCpVCkIN1yAVZbZmM3S62duH7nOEODStixq835zZcFLWVU1ZAs82YHo5xgC26YNrZfhuCG7WRja_Rib0ZLtzVC2Yf3DrHPsBpQpt7w</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Lee, Thomas Ming-Hung</creator><creator>Carles, Maria C</creator><creator>Hsing, I-Ming</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></search><sort><creationdate>20030101</creationdate><title>Microfabricated PCR-electrochemical device for simultaneous DNA amplification and detection</title><author>Lee, Thomas Ming-Hung ; Carles, Maria C ; Hsing, I-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-4352b75a291f80b37ad384222ded6529d494af641921d9b5b9b512d7ceab23f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Electrochemistry - instrumentation</topic><topic>Electrochemistry - methods</topic><topic>Glass - chemistry</topic><topic>Nanotechnology</topic><topic>Nucleic Acid Amplification Techniques - instrumentation</topic><topic>Nucleic Acid Amplification Techniques - methods</topic><topic>Nucleic Acid Hybridization</topic><topic>Oligonucleotide Probes - chemistry</topic><topic>Polymerase Chain Reaction - instrumentation</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Silicon - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Thomas Ming-Hung</creatorcontrib><creatorcontrib>Carles, Maria C</creatorcontrib><creatorcontrib>Hsing, I-Ming</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><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Thomas Ming-Hung</au><au>Carles, Maria C</au><au>Hsing, I-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microfabricated PCR-electrochemical device for simultaneous DNA amplification and detection</atitle><jtitle>Lab on a chip</jtitle><addtitle>Lab Chip</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>3</volume><issue>2</issue><spage>100</spage><epage>105</epage><pages>100-105</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>Microfabricated silicon/glass-based devices with functionalities of simultaneous polymerase chain reaction (PCR) target amplification and sequence-specific electrochemical (EC) detection have been successfully developed. The microchip-based device has a reaction chamber (volume of 8 microl) formed in a silicon substrate sealed by bonding to a glass substrate. Electrode materials such as gold and indium tin oxide (ITO) were patterned on the glass substrate and served as EC detection platforms where DNA probes were immobilized. Platinum temperature sensors and heaters were patterned on top of the silicon substrate for real-time, precise and rapid thermal cycling of the reaction chamber as well as for efficient target amplification by PCR. DNA analyses in the integrated PCR-EC microchip start with the asymmetric PCR amplification to produce single-stranded target amplicons, followed by immediate sequence-specific recognition of the PCR product as they hybridize to the probe-modified electrode. Two electrochemistry-based detection techniques including metal complex intercalators and nanogold particles are employed in the microdevice to achieve a sensitive detection of target DNA analytes. With the integrated PCR-EC microdevice, the detection of trace amounts of target DNA (as few as several hundred copies) is demonstrated. The ability to perform DNA amplification and EC sequence-specific product detection simultaneously in a single reaction chamber is a great leap towards the realization of a truly portable and integrated DNA analysis system.</abstract><cop>England</cop><pmid>15100790</pmid><doi>10.1039/b300799e</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | Royal Society of Chemistry Journals Archive (1841-2007); MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Electrochemistry - instrumentation Electrochemistry - methods Glass - chemistry Nanotechnology Nucleic Acid Amplification Techniques - instrumentation Nucleic Acid Amplification Techniques - methods Nucleic Acid Hybridization Oligonucleotide Probes - chemistry Polymerase Chain Reaction - instrumentation Polymerase Chain Reaction - methods Silicon - chemistry |
title | Microfabricated PCR-electrochemical device for simultaneous DNA amplification and detection |
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