4.7 Article

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

期刊

BIOSENSORS-BASEL
卷 12, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/bios12100868

关键词

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

资金

  1. National Natural Science Foundation of China [32171400]
  2. Natural Science Foundation of Guangdong Province [2020A1515010706]
  3. Shenzhen Science and Technology Innovation Committee [GXWD2020123015542700320200823111304001, JCYJ20180306172109024]

向作者/读者索取更多资源

This study developed a microfluidic device that allows dynamic variations of concentration in a channel and concentration distribution in multiple channels by adjusting the flow resistance using programmable pneumatic microvalves. The device offers superior application potentials in analytical chemistry, drug screening, and cell biology research.
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 mu m and membrane thicknesses of 20 and 30 mu m 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 R-h = ae(bP) 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 (C-k = -0.2k + 1) and nonlinear (C-k = (1/root 10)(k)) 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.

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