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
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