High flow rate microfluidic device for blood plasma separation using a range of temperatures

Lab Chip. 2010 Jan 21;10(2):211-9. doi: 10.1039/b904531g. Epub 2009 Nov 13.

Abstract

A hybrid microfluidic device that uses hydrodynamic forces to separate human plasma from blood cells has been designed and fabricated and the advantageous effects of temperature and flow rates are investigated in this paper. The blood separating device includes an inlet which is reduced by approximately 20 times to a small constrictor channel, which then opens out to a larger output channel with a small lateral channel for the collection of plasma. When tested the device separated plasma from whole blood using a wide range of flow rates, between 50 microl min(-1) and 200 microl min(-1), at the higher flow rates injected by hand and at temperatures ranging from 23 degrees C to 50 degrees C, the latter resulting in an increase in the cell-free layer of up to 250%. It was also tested continuously using between 5% and 40% erythrocytes in plasma and whole blood without blocking the channels or hemolysis of the cells. The mean percentage of plasma collected after separation was 3.47% from a sample of 1 ml. The percentage of cells removed from the plasma varied depending on the flow rate used, but at 37 degrees C ranged between 95.4 +/- 1% and 97.05 +/- 05% at 100 microl min(-1) and 200 microl min(-1), respectively. The change in temperature also had an effect on the number of cells removed from the plasma which was between 93.5 +/- 0.65% and 97.01 +/- 0.3% at 26.9 degrees C and 37 degrees C, respectively, using a flow rate of 100 microl min(-1). Due to its ability to operate in a wide range of conditions, it is envisaged that this device can be used in in vitro 'lab on a chip' applications, as well as a hand-held point of care (POC) device.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Component Removal / instrumentation*
  • Blood Specimen Collection / instrumentation*
  • Equipment Design
  • Equipment Failure Analysis
  • Heating / instrumentation*
  • Microfluidic Analytical Techniques / instrumentation*
  • Plasma / chemistry*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Temperature