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Design and Fabrication of a Ligase Detection Reaction (LDR) Microchip With an Integrated Passive Micromixer

[+] Author Affiliations
Tae Yoon Lee, Dimistris E. Nikitopoulos, Daniel S. Park, Steven A. Soper, Michael C. Murphy

Louisiana State University, Baton Rouge, LA

Paper No. IMECE2007-42216, pp. 125-130; 6 pages
doi:10.1115/IMECE2007-42216
From:
  • ASME 2007 International Mechanical Engineering Congress and Exposition
  • Volume 11: Micro and Nano Systems, Parts A and B
  • Seattle, Washington, USA, November 11–15, 2007
  • Conference Sponsors: ASME
  • ISBN: 0-7918-4305-X | eISBN: 0-7918-3812-9
  • Copyright © 2007 by ASME

abstract

The ligase detection reaction (LDR) is a technique that can distinguish low-abundant mutant DNAs from wild-type DNAs. LDR is usually carried out on DNAs amplified using the polymerase chain reaction (PCR). In the realization of modular microfluidic systems, the DNA output of the PCR handed off to the LDR chip needs to be mixed with LDR reagents before continuing the reaction. Polymer, continuous flow ligase detection reaction (CFLDR) devices with integrated passive micromixers, were designed, fabricated and tested. The devices each consisted of: a passive mixer for mixing a PCR sample, a cocktail of primers, and ligase, an enzyme of DNA; an incubator channel (95°C) for preheating the mixture; and a thermal cycling channel for the LDR. The devices were produced by hot embossing polycarbonate (PC) substrates with brass mold inserts manufactured by micro-milling. Experiments using food dyes showed that the appropriate mixture concentrations were delivered to the preheating channel in both the pulling and pushing modes.

Copyright © 2007 by ASME

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