IIT-M develops a lab-on-a-chip diagnostic device 
A team led by Prof. Ashis Kumar Sen, the corresponding 
author of the paper from the Department of Mechanical Engineering, IIT 
Madras, used a 2-cm-long microchannel device that employs capillary 
force to draw blood into the device to separate plasma from whole blood 
and test glucose level in diabetic patients.
The 
first part of the microchannel device has hydrophilic walls (top and two
 side walls) that help the blood sample to be drawn in through capillary
 force. But one centimetre away, all the four walls of the microchannel 
are hydrophobic. Like a drop of water on a Teflon surface, the blood 
comes together and forms a large contact angle (more than 90 degrees) 
when it enters the hydrophobic region. The forward movement of the blood
 is suddenly impeded and the blood cells tend to accumulate in the 
hydrophobic region of the microchannel. 
Unlike blood
 cells, the plasma with its low viscosity continues to move forward due 
to the momentum gained while passing through the hydrophilic region. 
“The blood cells slow down and then stop moving at the hydrophobic 
region and form a self built-in filter, while the plasma continues to 
move past the cells,” says Prof. Sen. “By creating a differential 
wetting behaviour in the microchannel we were able to separate the 
plasma from the blood cells.” Separating the plasma from blood cells is 
essential as it improves sensitivity and reliability. Most blood 
analyses are based on optical detection techniques, and the blood cells 
present tend to interfere with the optical path resulting in low 
sensitivity.
The device does not require any external
 or internal power as it relies on capillary force to draw blood and the
 separation of plasma from blood cells is achieved through differential 
wetting behaviour of the microchannel walls.
“Only
 5 microlitre of blood is required and in 15 minutes we get 450 
nanolitre of plasma which further increases with time. With suitable 
design modifications we have also achieved higher plasma volume up to 2 
microlitre in 15 min, which is adequate for detection of most analytes,”
 says M. Sneha Maria, the first author of the paper from the Department 
of Mechanical Engineering and Department of Biotechnology, IIT Madras. 
It takes 15-20 minutes to test the samples and get the results.
The
 detection platform for different diseases and conditions can be 
integrated within the device inside the hydrophobic region. “This is a 
proof-of-concept study so we used commercially available glucose test 
strips to detect glucose level in the blood samples,” says Maria. The 
sensitivity of the disposable device is comparable to conventional blood
 tests, says Prof. Sen.
Unlike the microchannel 
device used by the IIT team, commercial glucometers rely on whole blood 
for testing. Using whole blood can cause measurement errors due to 
various hematocrit levels (the ratio of the volume of red cells to the 
volume of whole blood). When the hematocrit levels are high the 
viscosity of blood is more and this leads to low glucose concentration 
and underestimation. Overestimation results when the hematocrit levels 
are low. “There is a likelihood of more than 10 per cent error in 
glucose detection when whole blood is used,” says Maria. 
The
 team is now testing the device for diagnosis of dengue. Currently, 
rapid diagnostic test kits (RDTs) either use whole blood which affects 
the sensitivity or centrifuged plasma for dengue detection. This is 
where the device can score over others. 
Prof. Sen is
 hopeful that the device can be used for parallel detection of analytes 
for several diseases using just one blood sample. “We intend to separate
 the plasma to multiple detection sites for studying several diseases in
 one go,” he says.
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