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A DNA biochip for on-the-spot multiplexed pathogen identification

Miniaturized integrated DNA analysis systems have largely been based on a multi-chamber design with microfluidic control to process the sample sequentially from one module to another. This microchip design in connection with optics involved hinders the deployment of this technology for point-of-care...

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Detalles Bibliográficos
Autores principales: Yeung, Siu-Wai, Lee, Thomas Ming-Hung, Cai, Hong, Hsing, I-Ming
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636451/
https://www.ncbi.nlm.nih.gov/pubmed/17000638
http://dx.doi.org/10.1093/nar/gkl702
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author Yeung, Siu-Wai
Lee, Thomas Ming-Hung
Cai, Hong
Hsing, I-Ming
author_facet Yeung, Siu-Wai
Lee, Thomas Ming-Hung
Cai, Hong
Hsing, I-Ming
author_sort Yeung, Siu-Wai
collection PubMed
description Miniaturized integrated DNA analysis systems have largely been based on a multi-chamber design with microfluidic control to process the sample sequentially from one module to another. This microchip design in connection with optics involved hinders the deployment of this technology for point-of-care applications. In this work, we demonstrate the implementation of sample preparation, DNA amplification, and electrochemical detection in a single silicon and glass-based microchamber and its application for the multiplexed detection of Escherichia coli and Bacillus subtilis cells. The microdevice has a thin-film heater and temperature sensor patterned on the silicon substrate. An array of indium tin oxide (ITO) electrodes was constructed within the microchamber as the transduction element. Oligonucleotide probes specific to the target amplicons are individually positioned at each ITO surface by electrochemical copolymerization of pyrrole and pyrrole−probe conjugate. These immobilized probes were stable to the thermal cycling process and were highly selective. The DNA-based identification of the two model pathogens involved a number of steps including a thermal lysis step, magnetic particle-based isolation of the target genomes, asymmetric PCR, and electrochemical sequence-specific detection using silver-enhanced gold nanoparticles. The microchamber platform described here offers a cost-effective and sample-to-answer technology for on-site monitoring of multiple pathogens.
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spelling pubmed-16364512006-11-29 A DNA biochip for on-the-spot multiplexed pathogen identification Yeung, Siu-Wai Lee, Thomas Ming-Hung Cai, Hong Hsing, I-Ming Nucleic Acids Res Methods Online Miniaturized integrated DNA analysis systems have largely been based on a multi-chamber design with microfluidic control to process the sample sequentially from one module to another. This microchip design in connection with optics involved hinders the deployment of this technology for point-of-care applications. In this work, we demonstrate the implementation of sample preparation, DNA amplification, and electrochemical detection in a single silicon and glass-based microchamber and its application for the multiplexed detection of Escherichia coli and Bacillus subtilis cells. The microdevice has a thin-film heater and temperature sensor patterned on the silicon substrate. An array of indium tin oxide (ITO) electrodes was constructed within the microchamber as the transduction element. Oligonucleotide probes specific to the target amplicons are individually positioned at each ITO surface by electrochemical copolymerization of pyrrole and pyrrole−probe conjugate. These immobilized probes were stable to the thermal cycling process and were highly selective. The DNA-based identification of the two model pathogens involved a number of steps including a thermal lysis step, magnetic particle-based isolation of the target genomes, asymmetric PCR, and electrochemical sequence-specific detection using silver-enhanced gold nanoparticles. The microchamber platform described here offers a cost-effective and sample-to-answer technology for on-site monitoring of multiple pathogens. Oxford University Press 2006-10 2006-09-25 /pmc/articles/PMC1636451/ /pubmed/17000638 http://dx.doi.org/10.1093/nar/gkl702 Text en © 2006 The Author(s)
spellingShingle Methods Online
Yeung, Siu-Wai
Lee, Thomas Ming-Hung
Cai, Hong
Hsing, I-Ming
A DNA biochip for on-the-spot multiplexed pathogen identification
title A DNA biochip for on-the-spot multiplexed pathogen identification
title_full A DNA biochip for on-the-spot multiplexed pathogen identification
title_fullStr A DNA biochip for on-the-spot multiplexed pathogen identification
title_full_unstemmed A DNA biochip for on-the-spot multiplexed pathogen identification
title_short A DNA biochip for on-the-spot multiplexed pathogen identification
title_sort dna biochip for on-the-spot multiplexed pathogen identification
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636451/
https://www.ncbi.nlm.nih.gov/pubmed/17000638
http://dx.doi.org/10.1093/nar/gkl702
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