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Taylor dispersion and the position-to-time conversion in microfluidic mixing devices
B Wunderlich1, D Nettels, B Schuler
1Department of Biochemistry, University of Zurich, Winterthurerstr. 190, 8057 Zurich, Switzerland. schuler@bioc.uzh.ch nettels@bioc.uzh.ch.
Lab on a Chip
|November 8, 2013
Summary
Accurately converting microfluidic channel positions to reaction times is crucial for studying biomolecular dynamics. This study introduces a novel method using 3D finite-element calculations to precisely account for Taylor dispersion, improving time resolution in microfluidic mixing devices.
Area of Science:
- Biomolecular dynamics
- Microfluidics
- Chemical kinetics
Background:
- Microfluidic mixing devices are essential for studying non-equilibrium biomolecular dynamics.
- Hydrodynamic focusing enables sub-millisecond reaction initiation in microfluidic systems.
- Accurate conversion of position to time is vital for kinetic analysis but complicated by Taylor dispersion.
Purpose of the Study:
- To develop an accurate position-to-time conversion method for microfluidic devices that accounts for Taylor dispersion across all time regimes.
- To quantify the impact of Taylor dispersion on the time resolution of microfluidic mixing devices, particularly for single-molecule fluorescence detection.
- To bridge the gap in position-to-time conversion accuracy between early and late time limits.
Main Methods:
- Detailed three-dimensional, time-dependent finite-element calculations were employed.
- The method provides an accurate position-to-time conversion, bridging early and late time regimes.
- Calculated velocity fields were validated against experimental dual-focus fluorescence correlation spectroscopy measurements.
Main Results:
- A robust method for position-to-time conversion in microfluidic devices was established, overcoming limitations of previous approaches.
- The study quantifies the influence of Taylor dispersion on the achievable time resolution.
- The finite-element calculations demonstrated high accuracy when compared to experimental data.
Conclusions:
- The developed method enables precise kinetic studies in microfluidic systems by accurately converting spatial positions to reaction times.
- Understanding and quantifying Taylor dispersion is critical for optimizing microfluidic device design and improving time resolution.
- This work enhances the utility of microfluidic devices for probing fast biomolecular processes.

