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Rheology of Soft and Rigid Micro Particles in Curved Microfluidic Channels

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Abstract

We investigated the rheological behavior of micro particles in inertial flow in a curved microfluidic channel. Different from the typical microfluidic regime operating at low Reynolds number, inertial flow provides hydrodynamic manipulation, namely inertial focusing of particles at high flow speeds. Primary influences of inertial flow on particle motions are several: repulsive force from the wall due to a pressure buildup in the constriction between the wall and the particle, shear gradient lift force due to the parabolic flow profile at microscale, and secondary drag force in the cross-sectional direction due to channel curvature. These forces result in particle moving across the streamlines to certain predictable equilibrium positions in the flow. With regard to soft particles, their flow behavior and equilibrium positions may deviate from the theoretical predictions based on rigid particles. This study provides a proof-of-concept of inertial focusing-based separation of particles with different deformability. We demonstrated its capability by separating yeast cells and polystyrene particles of similar sizes in a double spiral channel.

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References

  1. Pauling, L., Itano, H.A., Singer, S.J., Wells, I.C.: Sickle cell anemia, a molecular disease. Science 110, 543–548 (1949)

    Article  Google Scholar 

  2. Ingram, V.M.: A specific chemical difference between the globins of normal human and sickle cell anaemia hemoglobin. Nature 178, 792–794 (1956)

    Google Scholar 

  3. Bender, M.A., Douthitt Seibel, G.: Sickle cell disease. In: Pagon, R.A., et al. (eds.) GeneReviews®. University of Washington, Seattle, WA (1993)

    Google Scholar 

  4. National Heart LaBI: The management of sickle cell disease. NIH Publication. 02–2117 (2002)

    Google Scholar 

  5. Du, E., Diez-Silva, M., Kato, G.J., Dao, M., Suresh, S.: Kinetics of sickle cell biorheology and implications for painful vasoocclusive crisis. Proc. Natl. Acad. Sci. U. S. A. 112, 1422–1427 (2015)

    Article  Google Scholar 

  6. Di Carlo, D., Irimia, D., Tompkins, R.G., Toner, M.: Continuous inertial focusing, ordering, and separation of particles in microchannels. Proc. Natl. Acad. Sci. U. S. A. 104, 18892–18897 (2007)

    Article  Google Scholar 

  7. Di Carlo, D.: Inertial microfluidics. Lab Chip 9, 3038–3046 (2009)

    Google Scholar 

  8. Hur, S.C., Henderson-MacLennan, N.K., McCabe, E.R.B., Di Carlo, D.: Deformability-based cell classification and enrichment using inertial microfluidics. Lab Chip 11, 912–920 (2011)

    Article  Google Scholar 

  9. Mach, A.J., Di Carlo, D.: Continuous scalable blood filtration device using inertial microfluidics. Biotechnol. Bioeng. 107, 302–311 (2010)

    Article  Google Scholar 

  10. Hur, S.C., Brinckerhoff, T.Z., Walthers, C.M., Dunn, J.C.Y., Di Carlo, D.: Label-free enrichment of adrenal cortical progenitor cells using inertial microfluidics. PLoS One 7(10), e46550 (2012)

    Google Scholar 

  11. Jäggi, R.D., Sandoz, R., Effenhause, C.S.: Microfluidic depletion of red blood cells from whole blood in high-aspect-ratio microchannels. Microfluid. Nanofluid. 3, 7 (2007)

    Google Scholar 

  12. Nagrath, S., et al.: Isolation of rare circulating tumour cells in cancer patients by microchip technology. Nature 450, 1235–1239 (2007)

    Article  Google Scholar 

  13. Sun, J., et al.: Size-based hydrodynamic rare tumor cell separation in curved microfluidic channels. Biomicrofluidics 7, 11802 (2013)

    Article  Google Scholar 

  14. Sun, J., et al.: Double spiral microchannel for label-free tumor cell separation and enrichment. Lab Chip 12, 3952–3960 (2012)

    Article  Google Scholar 

  15. Chang-Yena, D.A., Galea, B.K.: An integrated optical oxygen sensor fabricated using rapid-prototyping techniques. Lab Chip 3, 5 (2003)

    Article  Google Scholar 

  16. Du, E., Mendelsohn, L., Nichols, J.S., Dao, M., Kato, G.J.: Quantification of anti-sickling effect of Aes-103 in sickle cell disease using an in vitro microfluidic assay. Blood 124, 2699 (2014)

    Article  Google Scholar 

Download references

Acknowledgement

This material is based upon work supported by the National Science Foundation under Grant No. 1464102.

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Correspondence to E. Du .

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© 2017 The Society for Experimental Mechanics, Inc.

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Liu, J., Qiang, Y., Mian, M., Xu, W., Du, E. (2017). Rheology of Soft and Rigid Micro Particles in Curved Microfluidic Channels. In: Korach, C., Tekalur, S., Zavattieri, P. (eds) Mechanics of Biological Systems and Materials, Volume 6. Conference Proceedings of the Society for Experimental Mechanics Series. Springer, Cham. https://doi.org/10.1007/978-3-319-41351-8_12

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  • DOI: https://doi.org/10.1007/978-3-319-41351-8_12

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-41350-1

  • Online ISBN: 978-3-319-41351-8

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