Microfluidic devices typically depend upon electrokinetic or traditional pressure methods to move microscopic amounts of fluid around a fixed microchip.
As just published as the cover story in Lab on a Chip engineering researchers at the University of Cincinnati have created a paradigm shift -- and moved some tiny channels in the process.
The field of microfluidics has been intensely investigated for nearly two decades, being traditionally explored within fixed geometries of continuous polymer or glass microchannels. None of the prior approaches was capable of creating any desired channel geometry and being able to keep that channel configuration intact without external stimulus.
With that capability, electrically induced channel functions could bridge the gap between the worlds of programmable droplet and continuous flow microfluidics.
Someone just bridged that "micromoat."
"So here we are working on displays, and creating cutting-edge techniques at moving colored fluids around, and we nearly overlooked the possibilities in lab-on-a-chip or biomedical areas," says Jason Heikenfeld, director of UC's Novel Devices Laboratory and an associate professor of electrical engineering in UC's College of Engineering and Applied Science. Heikenfeld has been making a name for himself -- and UC -- in the fields of photonics and electrofluidic display technology.
"This is where collaboration comes into play," Heikenfeld continues. "Here at UC we have several internationally known experts in microfluidics and lab-on-a-chip devices. We started collaborating with one of them, Ian Papautsky, and now we find ourselves in the middle of an exciting new application space."
"In microfluidics, we typically work with either continuous flows which give us high throughputs or droplets (digital flows) that can be manipulated electrically," says Papautsky, associate professor of electrical engineering. Papautsky is also director of UC's BioMicroSystems Lab and director of the Micro/Nano Fabrication Engineering Research Center. "In our new collaboration with Jason Heikenfeld, we are merging these two paradigms into a programmable microfluidic system. This is especially exciting because traditionally all lab-on-a-chip devices are limited by the predefined microchannel structure. A programmable microfluidics platform would offer an ability to reconfigure microchannel structure as needed for performing a wide range of biomedical assays, from DNA analysis to immunoassays, on the same chip."
This work was funded by NSF CBET Award #0729250 and NSF CAREER Award #0640964. A portion of this research was conducted at the Center for Nanophase Materials Sciences, which is sponsored at Oak Ridge National Laboratory by the Division of Scientific User Facilities, U.S. Department of Energy.
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