posted on 2007-03-15, 00:00authored byYong Zeng, D. Jed Harrison
We report on a biomolecular sieving system based on the
use of ordered colloidal arrays to define the sieve structure within a microfluidic device. A facile microfluidic
colloidal self-assembly strategy has been developed to
create ordered, robust, three-dimensional nanofluidic
sieves within microfluidic devices, with which fast separation of DNA and proteins of a wide size range was
achieved. Compared to conventional colloidal deposition
procedures, such as vertical deposition, this approach
features much faster assembling speed, the absence of
drying-caused cracks that may jeopardize the separation
performance, and better flexibility to couple with current
microfabrication techniques. The flexibility of pore size
enabled by this methodology provides separation of biomolecules with a wide size distribution, ranging from
proteins (20−200 kDa) to dsDNA (0.05−50 kbp). Under
moderate electric fields, complete separation can be
finished in minutes, with separation efficiency comparable
to gel/polymer-filled or micro-/nanofabricated microsystems. To our knowledge, this is the first demonstration
of size separation of biomolecules within self-assembled
ordered colloidal lattices embedded within a microfluidic
system.