• DocumentCode
    1421947
  • Title

    Closed chamber PCR chips for DNA amplification

  • Author

    Schabmueller, C.G.J. ; Lee, M.A. ; Evans, A.G.R. ; Brunnschweiler, A. ; Ensell, G.J. ; Leslie, D.L.

  • Author_Institution
    Dept. of Electron. & Comput. Sci., Southampton Univ., UK
  • Volume
    9
  • Issue
    6
  • fYear
    2000
  • fDate
    12/1/2000 12:00:00 AM
  • Firstpage
    259
  • Lastpage
    264
  • Abstract
    Small samples of DNA can be replicated (amplified) using the polymerase chain reaction (PCR) to produce sufficient quantities for analysis in the diagnosis of disease and in forensics. Low-cost single-shot PCR devices are desirable to avoid potential contamination of the sample reaction with products of a previous reaction. After explaining the principles of PCR amplification and optical detection of the products this paper describes the fabrication of a micromachined silicon/Pyrex-based chip for the PCR using standard micromachining processes. The reaction chamber has a volume of 1 μl. Pyrex is used for sealing the chamber and its transparency enables the use of optical detection methods. Incorporated heating and sensing elements allow fast heating and control of the chip. A Peltier element is used for cooling the chip to achieve rapid temperature cycling. Some performance data are presented
  • Keywords
    DNA; biomedical engineering; cooling; micromachining; polymers; DNA amplification; PCR amplification; Peltier element; biomedical engineering; chip cooling; closed chamber PCR chips; disease diagnosis; forensics; micromachined silicon/Pyrex-based chip; micromachining processes; optical detection methods; polymerase chain reaction; rapid temperature cycling; reaction chamber;
  • fLanguage
    English
  • Journal_Title
    Engineering Science and Education Journal
  • Publisher
    iet
  • ISSN
    0963-7346
  • Type

    jour

  • DOI
    10.1049/esej:20000605
  • Filename
    892875