• DocumentCode
    3098705
  • Title

    An electronic microfluidic switch using dielectrophoresis for control of microparticles

  • Author

    Javanmard, Mehdi ; Emaminejad, Sam ; Dutton, Robert ; Davis, Ronald W.

  • Author_Institution
    Stanford Genome Technol. Center, Stanford Univ., Stanford, CA, USA
  • fYear
    2011
  • fDate
    7-9 Dec. 2011
  • Firstpage
    1
  • Lastpage
    1
  • Abstract
    By making use of the advantages offered by micro and nanotechnologies, we aim to develop technologies which will decrease cost, increase assay speed, and improve limit of detection in biomolecular assays. Increasing sensitivity can enable earlier detection, and also can allow for identification of low-abundance markers that are not detectable with current techniques. We have previously developed a microfluidic platform capable of detecting enzyme activity at the attomolar level [1]. In order to transform this technology into a high throughput multiplexed assay, while maintaining low cost, instead of using microfluidic valves which requires extensive tubing and external pumps, it is desirable to achieve fluidic control of microparticles electrically. Using modern VLSI techniques, routing of hundreds or even thousands of electrodes and interconnects on a silicon chip is trivial compared to the requirement of connecting hundreds of tubes to a fluidic chip, which can become a plumbers nightmare.
  • Keywords
    VLSI; biomolecular electronics; electrophoresis; microfluidics; nanotechnology; sensitivity analysis; silicon; VLSI technique; attomolar level; biomolecular assay; dielectrophoresis; electronic microfluidic switch; enzyme activity detection; fluidic chip; high throughput multiplexed assay; low-abundance marker; microparticle control; microparticle fluidic control; microtechnology; nanotechnology; silicon chip; Dielectrophoresis; Electrodes; Force; Immune system; Microfluidics; Multiplexing; Switches;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Semiconductor Device Research Symposium (ISDRS), 2011 International
  • Conference_Location
    College Park, MD
  • Print_ISBN
    978-1-4577-1755-0
  • Type

    conf

  • DOI
    10.1109/ISDRS.2011.6135210
  • Filename
    6135210