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具有单一热源的对流双温PCR微流控装置的研究

Study of a convective two-temperature PCR microfluidics device with a single heat source
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摘要 为了克服传统连续流动聚合酶链式反应(PCR)微系统经常需要多个加热源来获取PCR所需要的温度,且集成或者非集成的泵系统也需要用来驱动PCR溶液连续流动,从而实现PCR扩增的缺点,研究了一种具有单一热源的对流双温PCR微系统。通过复合肋片技术在沟槽铜片上形成对流双温PCR所需要的温度,由流体密度差形成的自然对流来驱动闭环通道中连续流动PCR。实验表明:开发的微流控PCR能在45 min内扩增112 bp的大肠杆菌DNA片段。 To overcome shortcomings of the conventional continuous-flow PCR microsystems usually need multiple heat sources to provide temperatures for PCR,and the integrated or nonintegrated pumping systems are also required to drive the PCR solution to flow continuously,and thus the PCR is realized.A convective two-temperature PCR microfluidics with a single heat source is studied.The temperatures for this PCR microsystem are formed on the grooved copper flake by the combined fin technology.And,the large temperature differences needed for PCR induce the differences in the flow density,which under certain conditions can be used to transport the PCR solution within a closed-loop channel.The experiment demonstrates that the developed microfluidic PCR can amplify the 112 bp Escherichia coli DNA fragment in 45min.
作者 章春笋
出处 《传感器与微系统》 CSCD 北大核心 2011年第4期69-71,75,共4页 Transducer and Microsystem Technologies
基金 国家自然科学基金资助项目(30700155 61072030) 教育部"长江学者与创新团队计划"资助项目(IRT0829) 国家自然科学基金-广东联合基金重点资助项目(U0931005) 国家"863"计划资助项目(2007AA10Z204)
关键词 微流控 对流 聚合酶链式反应 DNA扩增 单一热源 microfluidics convective polymerase chain reaction(PCR) DNA amplification single heat source
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参考文献12

  • 1章春笋,徐进良.PCR生物芯片/微装置在微生物检测中应用研究[J].传感器技术,2005,24(1):1-3. 被引量:1
  • 2章春笋,徐进良.空域PCR芯片/微装置中温度控制技术[J].传感器技术,2004,23(10):8-10. 被引量:6
  • 3Hashimoto M, Chen P C, Mitchell M W, et al. Rapid PCR in a continuous flow device [ J ]. Lab on a Chip ,2004,4:638-645.
  • 4Krishnan M, Ugaz V M, Bums M A. PCR in a Rayleigh-B6nard convection cell[ J ]. Science,2002,298 : 793.
  • 5Krishnan M,Agrawal N,Bums M A,et al. Reactions and fluidics in miniaturized natural convection systems [ J J. Analytical Che- mistry ,2004,76:6254 -6265.
  • 6Chen Z, Qian S, Abrams W R, et al. Thermosiphon-based PCR reactor: Experiment and modeling [ J ]. Analytical Chemistry, 2004,76:3707 -3715.
  • 7Wheeler E K, Benett W, Stratton P, et al. Convectively driven po- lymerase chain reaction thermal cycler[ J ]. Analytical Chemistry, 2004,76:4011 -4016.
  • 8Agrawal N, Hassan Y A, Ugaz V M. A pocket-sized convective PCR thermocycler [ J ]. Angewandte Chemie International Edi- tion ,2007,46:4316 -4319.
  • 9Chung K H,Park S H,Choi Y H. A palmtop PCR system with a disposable polymer chip operated by the thermosiphon effect[ J ]. Lab on a Chip,2010,10:202-210.
  • 10Liu Jinfeng, Xing Da, Shen Xingyan, et al. Detection of genetically modified organisms by electrochemiluminescence PCR method [ J ]. Biosensors and Bioelectronics,2004,20:436 -441.

二级参考文献41

  • 1[1]Wittwer C T,Fillmore G C,Garling D J.Minimizing the time required for DNA amplification by efficient heat transfer to small samples [J].Anal Biochem,1990,186:328-331.
  • 2[2]Wilding P,Shoffner M A,Kricka L J.PCR in a silicon microstructure [J].Clin Chem,1994,40:1815-1818.
  • 3[3]Liu J,Enzelberger M,Quake S.A nanoliter rotary device for polymerase chain reaction [J].Electrophoresis,2002,23:1531-1536.
  • 4[4]Kricka L J,Wilding P.Microchip PCR [J].Anal Bioanal Chem,2003,377:820-825.
  • 5[5]Zhang Qintao,Wang Wenhui,Zhang Hongshen,et al.Temperature analysis of continuous-flow micro-PCR based on FEA [J].Sens Actuat B,2002,82:75-81.
  • 6[6]Yu Xiaomei,Zhang Dacheng,Li Ting,et al.3-D microarrays biochips for DNA amplification in polydimethylsiloxane (PDMS) elestomer [J].Sens Actuat A,2003,108:103-107.
  • 7[7]Zhao Zhan,Cui Zheng,Cui Dafu,et al.Monolithically integrated PCR biochip for DNA amplification [J].Sens Actuat A,2003,108:162-167.
  • 8[9]Larzul M D.Apparatus for repeated automatic execution of a thermal cycle for treatment of samples [P].US patent: 5176203,1993-01-05.
  • 9[10]Nakano H,Matsuda K,Yohda M,et al.High speed polymerase chain reaction in constant flow [J].Biosci Biotechnol Biochem,1994,58(2):349-352
  • 10[11]Kopp M U,de Mello A J,Manz A.Chemical amplification: continuous-flow PCR on a chip [J].Science,1998,280:1046-1048.

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