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Updated: Jul 27, 2025

A Microfluidic-based Hydrodynamic Trap for Single Particles
Published on: January 21, 2011
Low-cost acoustic force trap in a microfluidic channel
Vi-Hung Tsan1, Daniel Fan1, Sabina Caneva1
1Faculty of Mechanical, Materials, and Maritime Engineering, Technische Universiteit Delft, Delft 2628CD, The Netherlands.
We developed a low-cost microfluidic flow cell using off-the-shelf parts to trap and manipulate micro-beads and cells using acoustophoretic force. This device enables precise control of micrometer-scale objects for applications in biophysics and cell mechanics.
Area of Science:
- Microfluidics
- Acoustic manipulation
- Biophysics
Background:
- Microfluidic devices are essential for manipulating small-scale objects.
- Acoustophoretic forces offer a label-free method for particle manipulation.
- Developing low-cost, accessible microfluidic tools is crucial for broader research adoption.
Purpose of the Study:
- To design and fabricate a low-cost microfluidic flow cell for acoustophoretic manipulation.
- To demonstrate the trapping and positional control of micro-beads.
- To establish a foundation for force spectroscopy applications on biomolecules.
Main Methods:
- Fabrication of a glass-based microfluidic cell using inexpensive, off-the-shelf components.
- Integration of a piezo actuator to generate acoustophoretic forces.
- Utilizing double-sided tape and nail polish for device leak-tightness.
Main Results:
- Successfully trapped 1.5 μm polystyrene micro-beads in a 100 μm deep channel at 7.5 MHz with 23.7 Vpp.
- Achieved precise axial positioning of trapped beads at 50 ± 0.1 μm depth.
- Measured an approximate trap stiffness of 0.6 pN/μm.
Conclusions:
- A cost-effective microfluidic device capable of acoustophoretic manipulation of micro-scale objects has been developed.
- The device allows for controlled manipulation of beads and cells, with potential applications in force spectroscopy.
- This technology can be integrated with super-resolution imaging for advanced studies of DNA mechanics and protein-DNA interactions.
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