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Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends

The possibility of performing fast and small-volume nucleic acid amplification and analysis on a single chip has attracted great interest. Devices based on this idea, referred to as micro total analysis, microfluidic analysis, or simply ‘Lab on a chip’ systems, have witnessed steady advances over th...

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Detalles Bibliográficos
Autores principales: Zhang, Chunsun, Xing, Da
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934988/
https://www.ncbi.nlm.nih.gov/pubmed/17576684
http://dx.doi.org/10.1093/nar/gkm389
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author Zhang, Chunsun
Xing, Da
author_facet Zhang, Chunsun
Xing, Da
author_sort Zhang, Chunsun
collection PubMed
description The possibility of performing fast and small-volume nucleic acid amplification and analysis on a single chip has attracted great interest. Devices based on this idea, referred to as micro total analysis, microfluidic analysis, or simply ‘Lab on a chip’ systems, have witnessed steady advances over the last several years. Here, we summarize recent research on chip substrates, surface treatments, PCR reaction volume and speed, architecture, approaches to eliminating cross-contamination and control and measurement of temperature and liquid flow. We also discuss product-detection methods, integration of functional components, biological samples used in PCR chips, potential applications and other practical issues related to implementation of lab-on-a-chip technologies.
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spelling pubmed-19349882007-08-07 Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends Zhang, Chunsun Xing, Da Nucleic Acids Res Survey and Summary The possibility of performing fast and small-volume nucleic acid amplification and analysis on a single chip has attracted great interest. Devices based on this idea, referred to as micro total analysis, microfluidic analysis, or simply ‘Lab on a chip’ systems, have witnessed steady advances over the last several years. Here, we summarize recent research on chip substrates, surface treatments, PCR reaction volume and speed, architecture, approaches to eliminating cross-contamination and control and measurement of temperature and liquid flow. We also discuss product-detection methods, integration of functional components, biological samples used in PCR chips, potential applications and other practical issues related to implementation of lab-on-a-chip technologies. Oxford University Press 2007-07 2007-06-18 /pmc/articles/PMC1934988/ /pubmed/17576684 http://dx.doi.org/10.1093/nar/gkm389 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Survey and Summary
Zhang, Chunsun
Xing, Da
Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title_full Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title_fullStr Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title_full_unstemmed Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title_short Miniaturized PCR chips for nucleic acid amplification and analysis: latest advances and future trends
title_sort miniaturized pcr chips for nucleic acid amplification and analysis: latest advances and future trends
topic Survey and Summary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934988/
https://www.ncbi.nlm.nih.gov/pubmed/17576684
http://dx.doi.org/10.1093/nar/gkm389
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