Previous researchers have used 3D printers to make microfluidics, but not on this scale
Researchers at BYU are the first to 3D-print a viable microfluidic device small enough to be effective at a scale much less than 100 micrometers. Microfluidic devices are tiny chips that can sort out disease biomarkers, cells and other small structures in samples like blood by using microscopic channels incorporated into the devices.
The accomplishment, which is a major breakthrough toward mass-producing the medical diagnostic devices cheaply, is detailed in the latest issue of the academic journal Lab on a Chip. Researchers Greg Nordin, a BYU electrical engineering professor, and Adam Woolley, a BYU chemistry professor, say the key to their innovation was two-fold:
- Building their own 3D printer to print at a much higher resolution
- Using a new, specifically designed, low-cost, custom resin
“Others have 3D-printed fluidic channels, but they haven’t been able to make them small enough for microfluidics,” Nordin said. “So we decided to make our own 3D printer and research a resin that could do it.”
Their work has produced labs on a chip with flow channel cross sections as small as 18 micrometers by 20 micrometers. Previous efforts to 3D-print microfluidic devices have failed to achieve success smaller than 100 micrometers. The researchers’ 3D printer uses a 385 nm LED, which dramatically increases the available selection of UV absorbers for resin formulation compared to 3D printers with 405 nm LEDs.
Nordin said the advantages of 3D printing for microfluidic device fabrication are already well-known and that their method, digital light processing stereolithography (DLP-SLA), is an especially promising lower-cost approach. DLP-SLA uses a micromirror array chip, like those in most consumer projectors, to dynamically create the optical pattern for each layer during layer-by-layer printing of a device.
Researchers say they are laying the foundation for 3D printing to challenge the dominance of conventional methods — soft lithography and hot embossing — of microfluidic prototyping and development.
“We’re deliberately trying to start a revolution in how microfluidic devices are fabricated,” Nordin said.
Woolley’s research interests in microfluidics focus on using lab-on-a-chip devices to detect biomarkers related to preterm birth. To that end, he and Nordin just submitted a proposal to the National Institutes of Health to develop the approach in this paper for preterm birth prediction.
Woolley said the paper represents an improvement of a factor of 100 on the size of features that are now possible in 3D printed microfluidics. It also cuts down on time and hassle: the BYU-authored approach can create a device in 30 minutes’ time and doesn’t require the use of clean rooms — a special lab environment free from dust and other contaminants.
“It’s not just a little step; it’s a huge leap from one size regime to a previously inaccessible size regime for 3D printing,” Woolley said. “It opens up a lot of doors for making microfluidics more easily and inexpensively.”
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