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PCR microfluidic devices for DNA amplification
Zhang, CS; Xu, JL; Ma, WL; Zheng, WL
2006-05-01
发表期刊BIOTECHNOLOGY ADVANCES
卷号24期号:3页码:243-284
摘要The miniaturization of biological and chemical analytical devices by micro-electro-mechanical-systems (MEMS) technology has posed a vital influence on such fields as medical diagnostics, microbial detection and other bio-analysis. Among many miniaturized analytical devices, the polymerase chain reaction (PCR) microchip/microdevices are studied extensively, and thus great progress has been made on aspects of on-chip micromachining (fabrication, bonding and sealing), choice of substrate materials, surface chemistry and architecture of reaction vessel, handling of necessary sample fluid, controlling of three or two-step temperature thermocycling, detection of amplified nucleic acid products, integration with other analytical functional units such as sample preparation, capillary electrophoresis (CE), DNA microarray hybridization, etc. However, little has been done on the review of above-mentioned facets of the PCR microchips/microdevices including the two formats of flow-through and stationary chamber in spite of several earlier reviews [Zorbas, H. Miniature continuous-flow polymerase chain reaction: a breakthrough? Angew Chem Int Ed 1999; 38 (8):1055-1058; Krishnan, M., Namasivayam, V., Lin, R., Pal, R., Burns, M.A. Microfabricated reaction and separation systems. Curr Opin Biotechnol 2001; 12:92-98; Schneega beta, 1., Kohler, J.M. Flow-through polymerase chain reactions in chip themocyclers. Rev Mol Biotechnol 2001; 82:101-121; deMello, A.J. DNA amplification: does 'small' really mean 'efficient'? Lab Chip 2001; 1: 24N-29N; Marietta, Jr. R. MEMS for bio-assays. Biomed Microdevices 2002; 4 (2):77-87; deMello AJ. Microfluidics: DNA amplification moves on. Nature 2003; 422:28-29; Kricka, L.J., Wilding, P. Microchip PCR. Anal BioAnal Chem 2003; 377:820-825]. In this review, we survey the advances of the above aspects among the PCR microfluidic devices in detail. Finally, we also illuminate the potential and practical applications of PCR microfluidics to some fields such as microbial detection and disease diagnosis, based on the DNA/RNA templates used in PCR microfluidics. It is noted, especially, that this review is to help a novice in the field of on-chip PCR amplification to more easily find the original papers, because this review covers almost all of the papers related to on-chip PCR microfluidics. (c) 2005 Elsevier Inc. All rights reserved.
文章类型Review
关键词Polymerase Chain Reaction (Pcr) Microfluidics Dna Amplification
WOS标题词Science & Technology ; Life Sciences & Biomedicine
DOI10.1016/j.biotechadv.2005.10.002
研究领域[WOS]Biotechnology & Applied Microbiology
关键词[WOS]POLYMERASE-CHAIN-REACTION ; MULTICHAMBER THERMAL CYCLER ; PRECISE TEMPERATURE CONTROL ; GEL-FILLED CAPILLARIES ; NUCLEIC-ACID ANALYZER ; C VIRUS AMPLIFICATION ; SILICON-GLASS CHIPS ; CONTINUOUS-FLOW PCR ; MICROCHIP-BASED PCR ; ELECTROPHORETIC ANALYSIS
收录类别SCI
语种英语
WOS类目Biotechnology & Applied Microbiology
WOS记录号WOS:000237178600001
引用统计
被引频次:355[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.giec.ac.cn/handle/344007/10255
专题中国科学院广州能源研究所
作者单位1.Chinese Acad Sci, Micro Energy Syst Lab, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
2.Univ Sci & Technol China, Dept Thermal Sci & Energy Engn, Hefei 230026, Peoples R China
3.First Mil Med Univ, Inst Mol Biol, Key Lab DNA Chips, Guangzhou 510515, Peoples R China
4.First Mil Med Univ, Dept Biochem & Mol Biol, Guangzhou 510515, Peoples R China
5.First Mil Med Univ, Inst Genet Engn PLA, Key Lab DNA Chips, Guangzhou 510515, Peoples R China
6.First Mil Med Univ, Inst Mol Oncol, Liu Hua Qiao Hosp Med Ctr, Guangzhou 510515, Peoples R China
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Zhang, CS,Xu, JL,Ma, WL,et al. PCR microfluidic devices for DNA amplification[J]. BIOTECHNOLOGY ADVANCES,2006,24(3):243-284.
APA Zhang, CS,Xu, JL,Ma, WL,&Zheng, WL.(2006).PCR microfluidic devices for DNA amplification.BIOTECHNOLOGY ADVANCES,24(3),243-284.
MLA Zhang, CS,et al."PCR microfluidic devices for DNA amplification".BIOTECHNOLOGY ADVANCES 24.3(2006):243-284.
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