Rapid, robust, and economical fabrication of fluidic microchannels is of fundamental importance for the successful development of disposable lab-on-a-chip devices. In this work, we present a solvent-actuated bonding method for fabricating polymeric microfluidic devices at room temperature. A PMMA sheet with an imprinted microchannel was clamped to a blank PMMA sheet, and then 80 +/- 5 muL of acetone (bonding solvent) was introduced at one end of the fluidic channel and aspirated out at the other end. As the solvent moved down the channel, capillary forces drew a fraction of the solvent into the interstitial space between the two polymeric substrates. After aspiration, the assembly was incubated in the clamp for 5 min for effective bond formation. The quantity of the bonding solvent, its water content and flow rate, along with residence time in the channel were found to have significant impact on the bond quality and the channel integrity. Microfluidic electrophoretic separations of a 400-base DNA ladder were performed in devices fabricated using this method in less than 8 min with efficiencies routinely between 2 x 10(6) and 3 x 10(6) plates/m. The simplicity and economy of this technique make it amenable for automation and mass production, which could make polymeric substrates more attractive for single-use chemical analysis devices.
Temperature mapping based on fluorescent signal intensity ratios is a widely used noncontact approach for investigating temperature distributions in various systems. This noninvasive method is especially useful for applications, such as microfluidics, where accurate temperature measurements are difficult with conventional physical probes. However, the application of a calibration equation to relate fluorescence intensity ratio to temperature is not straightforward when the reference temperature in a given application is different than the one used to derive the calibration equation. In this report, we develop and validate generalized calibration equations that can be applied for any value of reference temperature. Our analysis shows that a simple linear correction for a 40 degrees C reference temperature produces errors in measured temperatures between -3 to 8 degrees C for three previously published sets of cubic calibration equations. On the other hand, corrections based on an exact solution of these equations restrict the errors to those inherent in the calibration equations. The methods described here are demonstrated for cubic calibration equations derived by three different groups, but the general method can be applied to other dyes and calibration equations.
The ability to selectively and precisely control the temperature of fluid volumes ranging from a few microliters to sub-nanoliters in microfluidic networks is vital for a wide range of applications in micro total analysis systems (µTAS). In this work, we characterize and model the performance of a thin film microwave transmission line integrated with a microfluidic channel to heat fluids with relevant buffer salt concentrations over a wide range of frequencies. A microchannel fabricated in poly(dimethylsiloxane) (PDMS) is aligned with a thin film microwave transmission line in a coplanar waveguide (CPW) configuration. The electromagnetic fields localized in the gap between the signal and ground lines of the transmission line dielectrically heat the fluid in the selected region of the microchannel. Microwave S-parameter measurements and optical fluorescence-based temperature measurements are used with a theoretical model developed based on classical microwave absorption theory to fully characterize the temperature rise of the fluid. We observe a 0.95 • C mW −1 temperature rise at 15 GHz and confirm that the temperature rise of the fluid is predominantly due to microwave dielectric heating.
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