New optofluidic platform features tunable optics and novel 'lightvalves'
- Date:
- September 14, 2016
- Source:
- University of California, Santa Cruz
- Summary:
- Novel technology combines high-performance microfluidics for sample processing with dynamic optical tuning and switching, all on a low-cost "chip" made of a flexible silicone material.
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For well over a decade, electrical engineer Holger Schmidt has been developing devices for optical analysis of samples on integrated chip-based platforms, with applications in areas such as biological sensors, virus detection, and chemical analysis. The latest device from his lab is based on novel technology that combines high-performance microfluidics for sample processing with dynamic optical tuning and switching, all on a low-cost "chip" made of a flexible silicone material.
In previous devices from Schmidt's lab, optical functions were built into silicon chips using the same fabrication technology used to make computer chips. The new device is made entirely of polydimethylsiloxane (PDMS), a soft, flexible material used in microfluidics as well as in products such as contact lenses and medical devices.
"We can use this fabrication method now to build an all-in-one device that allows us to do biological sample processing and optical detection on one chip," said Schmidt, the Kapany Professor of Optoelectronics and director of the W. M. Keck Center for Nanoscale Optofluidics at UC Santa Cruz.
The flexibility of PDMS allows for novel ways of controlling both light and fluids on the chip. Using multilayer soft lithography techniques, senior graduate student Joshua Parks built chips containing both solid-core and hollow-core waveguides for guiding light signals, as well as fluidic microvalves to control the movement of liquid samples. Schmidt and Parks also developed a special microvalve that functions as a "lightvalve," controlling the flow of both light and fluids.
"That opens up a whole new set of functions that we couldn't do on a silicon chip," Schmidt said. "The lightvalve is the most exciting element. In additional to a simple on-off switch, we built a moveable optical trap for analysis of biological particles such as viruses or bacteria."
Parks and Schmidt reported the results of initial experiments with the new device in a paper published September 6 in Nature Scientific Reports.
In a previous study, Schmidt, Parks, and colleagues at BYU and UC Berkeley demonstrated a hybrid device in which a PDMS microfluidic chip for sample preparation was integrated with a silicon-based optofluidic chip for optical detection of viral pathogens. The new device combines both functions on the same chip. In addition, Schmidt said, the materials are relatively inexpensive, allowing rapid prototyping of devices.
"We can do the full chain of fabrication here in our lab, and we can make new devices very quickly," he said.
Schmidt said the potential applications for this technology include a wide range of biological sensors and analytical devices. For viral diagnostic assays, for example, fluorescently labeled antibodies can be used to tag specific viral strains for optical detection. In a recent paper, Schmidt and colleagues demonstrated detection and identification of different flu strains using fluorescence detection in a multi-mode interference (MMI) waveguide. With the new device, they showed that they can actively tune an MMI waveguide on the chip.
The dynamic tuning of the optofluidic device is achieved by applying pressure to the optofluidic channel, changing its dimensions and thereby altering its photonic properties. "We can actually tune the spot pattern made in the channel by the interference waveguide, which we couldn't do with the silicon chip," Schmidt said.
Story Source:
Materials provided by University of California, Santa Cruz. Original written by Tim Stephens. Note: Content may be edited for style and length.
Journal Reference:
- Joshua W. Parks, Holger Schmidt. Flexible optofluidic waveguide platform with multi-dimensional reconfigurability. Scientific Reports, 2016; 6: 33008 DOI: 10.1038/srep33008
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