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Generation of Dynamic Concentration Profile Using A Microfluidic Device Integrating Pneumatic Microvalves

  • Chang Chen
  • , Panpan Li
  • , Tianruo Guo
  • , Siyuan Chen
  • , Dong Xu
  • , Huaying Chen*
  • *Corresponding author for this work
  • Harbin Institute of Technology Shenzhen
  • Harbin Institute of Technology
  • University of New South Wales

Research output: Contribution to journalArticlepeer-review

Abstract

Generating and maintaining the concentration dilutions of diffusible molecules in microchannels is critical for high-throughput chemical and biological analysis. Conventional serial network microfluidic technologies can generate high orders of arbitrary concentrations by a predefined microchannel network. However, a previous design requires a large occupancy area and is unable to dynamically generate different profiles in the same chip, limiting its applications. This study developed a microfluidic device enabling dynamic variations of both the concentration in the same channel and the concentration distribution in multiple channels by adjusting the flow resistance using programmable pneumatic microvalves. The key component (the pneumatic microvalve) allowed dynamic adjustment of the concentration profile but occupied a tiny space. Additionally, a Matlab program was developed to calculate the flow rates and flow resistance of various sections of the device, which provided theoretical guidance for dimension design. In silico investigations were conducted to evaluate the microvalve deformation with widths from 100 to 300 µm and membrane thicknesses of 20 and 30 µm under the activation pressures between 0 and 2000 mbar. The flow resistance of the deformed valve was studied both numerically and experimentally and an empirical model for valve flow resistance with the form of (Formula presented.) was proposed. Afterward, the fluid flow in the valve region was characterized using Micro PIV to further demonstrate the adjustment mechanism of the flow resistance. Then, the herringbone structures were employed for fast mixing to allow both quick variation of concentration and minor space usage of the channel network. Finally, an empirical formula-supported computational program was developed to provide the activation pressures required for the specific concentration profile. Both linear ((Formula presented.) = −0.2k + 1) and nonlinear (Formula presented.) = (Formula presented.) concentration distribution in four channels were varied using the same device by adjusting microvalves. The device demonstrated the capability to control the concentration profile dynamically in a small space, offering superior application potentials in analytical chemistry, drug screening, and cell biology research.

Original languageEnglish
Article number868
JournalBiosensors
Volume12
Issue number10
DOIs
StatePublished - Oct 2022
Externally publishedYes

Keywords

  • concentration profile
  • dynamic
  • fluid resistance
  • microfluidic
  • pneumatic microvalves
  • programmable

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