David W Inglis

Summary

Affiliation: Macquarie University
Country: Australia

Publications

  1. ncbi request reprint Determining blood cell size using microfluidic hydrodynamics
    David W Inglis
    Princeton Institute for the Science and Technology of Materials PRISM, Department of Electrical Engineering, Princeton University, Princeton, NJ 08544, USA
    J Immunol Methods 329:151-6. 2008
  2. pmc Hydrodynamic metamaterials: microfabricated arrays to steer, refract, and focus streams of biomaterials
    Keith J Morton
    Departments of Electrical Engineering and Physics, Princeton University, Princeton, NJ 08544 1014, USA
    Proc Natl Acad Sci U S A 105:7434-8. 2008
  3. doi request reprint Microfluidic device for label-free measurement of platelet activation
    David W Inglis
    Department of Physics, Macquarie University, Sydney, NSW 2109, Australia
    Lab Chip 8:925-31. 2008
  4. doi request reprint Crossing microfluidic streamlines to lyse, label and wash cells
    Keith J Morton
    Princeton Institute for the Science and Technology of Materials, Department of Electrical Engineering, Princeton University, NJ, USA
    Lab Chip 8:1448-53. 2008
  5. pmc Deterministic hydrodynamics: taking blood apart
    John A Davis
    Princeton Institute for the Science and Technology of Materials, Princeton University, Princeton, NJ 08544, USA
    Proc Natl Acad Sci U S A 103:14779-84. 2006
  6. ncbi request reprint Critical particle size for fractionation by deterministic lateral displacement
    David W Inglis
    Princeton Institute for the Science and Technology of Materials, PRISM Princeton University, Princeton, NJ 08544, USA
    Lab Chip 6:655-8. 2006

Collaborators

  • Stephen Y Chou
  • Keith J Morton
  • James C Sturm
  • Robert H Austin
  • Ophelia K Tsui
  • Kevin Loutherback
  • John A Davis
  • Lotien R Huang
  • David A Lawrence

Detail Information

Publications6

  1. ncbi request reprint Determining blood cell size using microfluidic hydrodynamics
    David W Inglis
    Princeton Institute for the Science and Technology of Materials PRISM, Department of Electrical Engineering, Princeton University, Princeton, NJ 08544, USA
    J Immunol Methods 329:151-6. 2008
    ..Together the results demonstrate a microfluidic device that performs some of the measurement and separation tasks of a flow cytometer but at a potentially lower cost and complexity...
  2. pmc Hydrodynamic metamaterials: microfabricated arrays to steer, refract, and focus streams of biomaterials
    Keith J Morton
    Departments of Electrical Engineering and Physics, Princeton University, Princeton, NJ 08544 1014, USA
    Proc Natl Acad Sci U S A 105:7434-8. 2008
    ..The unusual aspects of these modular, microfluidic metamaterials form a rich design toolkit for mixing, separating, and analyzing cells and functional beads on-chip...
  3. doi request reprint Microfluidic device for label-free measurement of platelet activation
    David W Inglis
    Department of Physics, Macquarie University, Sydney, NSW 2109, Australia
    Lab Chip 8:925-31. 2008
    ..We infer that the well known morphological changes that occur during activation are causing the observed increase in size...
  4. doi request reprint Crossing microfluidic streamlines to lyse, label and wash cells
    Keith J Morton
    Princeton Institute for the Science and Technology of Materials, Department of Electrical Engineering, Princeton University, NJ, USA
    Lab Chip 8:1448-53. 2008
    ..The washing capabilities of this method are particularly valuable because they allow many analytical or treatment procedures to be cascaded on a single device while still effectively isolating their reagents from cross-contamination...
  5. pmc Deterministic hydrodynamics: taking blood apart
    John A Davis
    Princeton Institute for the Science and Technology of Materials, Princeton University, Princeton, NJ 08544, USA
    Proc Natl Acad Sci U S A 103:14779-84. 2006
    ..Using a second design, we demonstrated the separation of blood plasma from the blood cells (white, red, and platelets) with virtually no dilution of the plasma and no cellular contamination of the plasma...
  6. ncbi request reprint Critical particle size for fractionation by deterministic lateral displacement
    David W Inglis
    Princeton Institute for the Science and Technology of Materials, PRISM Princeton University, Princeton, NJ 08544, USA
    Lab Chip 6:655-8. 2006
    ..In general the critical particle diameter is much smaller than the gap, which prevents clogging. The model is supported by data with particles from 2.3 to 22 microm...