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Biomicrofluidics 5, 044111 (2011); http://dx.doi.org/10.1063/1.3664691 (10 pages)

Microfluidic concentration of bacteria by on-chip electrophoresis

Dietmar Puchberger-Enengl1,2, Susann Podszun2, Helene Heinz2, Carsten Hermann2, Paul Vulto3, and Gerald A. Urban2

1Institute of Sensor and Actuator Systems (ISAS), Vienna University of Technology, Vienna, Austria
2Laboratory for Sensors, Department of Microsystems Engineering (IMTEK), Albert-Ludwigs-Universitäat Freiburg, Georges-Koehler-Allee 103, Freiburg, Germany
3Division of Analytical Biosciences, Netherlands Metabolomics Centre/LACDR, Leiden University, Leiden, Netherlands

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(Received 13 September 2011; accepted 31 October 2011; published online 2 December 2011)

In this contribution, we present a system for efficient preconcentration of pathogens without affecting their viability. Development of miniaturized molecular diagnostic kits requires concentration of the sample, molecule extraction, amplification, and detection. In consequence of low analyte concentrations in real-world samples, preconcentration is a critical step within this workflow. Bacteria and viruses exhibit a negative surface charge and thus can be electrophoretically captured from a continuous flow. The concept of phaseguides was applied to define gel membranes, which enable effective and reversible collection of the target species. E. coli of the strains XL1-blue and K12 were used to evaluate the performance of the device. By suppression of the electroosmotic flow both strains were captured with efficiencies of up to 99%. At a continuous flow of 15 μl/min concentration factors of 50.17 ± 2.23 and 47.36 ± 1.72 were achieved in less than 27 min for XL1-blue and K12, respectively. These results indicate that free flow electrophoresis enables efficient concentration of bacteria and the presented device can contribute to rapid analyses of swab-derived samples.

© 2011 American Institute of Physics

Article Outline

  1. INTRODUCTION
  2. THEORY
  3. DESIGN
  4. MATERIAL AND METHODS
    1. Finite element simulations
    2. Chip fabrication
    3. Sample preparation
    4. Experimental setup
  5. RESULTS AND DISCUSSION
  6. CONCLUSION

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KEYWORDS and PACS

PACS

  • 87.80.Ek

    Mechanical and micromechanical techniques

  • 87.15.Tt

    Electrophoresis

  • 85.85.+j

    Micro- and nano-electromechanical systems (MEMS/NEMS) and devices

ARTICLE DATA

PUBLICATION DATA

ISSN

1932-1058 (online)

For access to fully linked references, you need to log in.
    C.-P. Jen and H.-H. Chang, Biomicrofluidics 5, 034101 (2011)BIOMGB000005000003034101000001.

    C. Church, J. Zhu, G. Huang, T.-R. Tzeng, and X. Xuan, Biomicrofluidics 4, 44101 (2010)BIOMGB000004000004044101000001.

    D. Hou, S. Maheshwari, and H.-C. Chang, Biomicrofluidics 1, 14106 (2007)BIOMGB000001000001014106000001.

    M. Koklu, S. Park, S. D. Pillai, and A. Beskok, Biomicrofluidics 4 (2010)BIOMGB000004000003034107000001.

    I.-F. Cheng, H.-C. Chang, D. Hou, and H.-C. Chang, Biomicrofluidics 1, 21503 (2007)BIOMGB000001000002021503000001.

    R. S. W. Thomas, P. D. Mitchell, R. O. C. Oreffo, and H. Morgan, Biomicrofluidics 4, 022806 (2010)BIOMGB000004000002022806000001


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