Submillisecond mixing in a continuous-flow, microfluidic mixer utilizing mid-infrared hyperspectral imaging detection

• Authors: Drew P. Kise, Emory University; Donny Magana, Emory University; Michael Reddish, Emory University; Richard Dyer, Emory University
• Journal Title: Lab on a Chip
• Volume: Volume 14, Number 3
• Publisher: Royal Society of Chemistry | 2014-02-07, Pages 584-591
• Type of Work: Article | Post-print: After Peer Review
• Publisher DOI: http://doi.org/10.1039/c3lc51171e
• Subjects: Biophysics, General; Engineering, Biomedical; Biology, Molecular
• Keywords: Adenosine Monophosphate; Deuterium Oxide; Microfluidic Analytical Techniques; Models, Theoretical; Spectrophotometry, Infrared; Time Factors; Water

Abstract

We report a continuous-flow, microfluidic mixer utilizing mid-infrared hyperspectral imaging detection, with an experimentally determined, submillisecond mixing time. The simple and robust mixer design has the microfluidic channels cut through a polymer spacer that is sandwiched between two IR transparent windows. The mixer hydrodynamically focuses the sample stream with two side flow channels, squeezing it into a thin jet and initiating mixing through diffusion and advection. The detection system generates a mid-infrared hyperspectral absorbance image of the microfluidic sample stream. Calibration of the hyperspectral image yields the mid-IR absorbance spectrum of the sample versus time. A mixing time of 269 μs was measured for a pD jump from 3.2 to above 4.5 in a D2O sample solution of adenosine monophosphate (AMP), which acts as an infrared pD indicator. The mixer was further characterized by comparing experimental results with a simulation of the mixing of an H 2O sample stream with a D2O sheath flow, showing good agreement between the two. The IR microfluidic mixer eliminates the need for fluorescence labeling of proteins with bulky, interfering dyes, because it uses the intrinsic IR absorbance of the molecules of interest, and the structural specificity of IR spectroscopy to follow specific chemical changes such as the protonation state of AMP.