A microfluidic generator of dynamic shear stress and biochemical signals based on autonomously oscillatory flow. Issue 21 (29th July 2021)

• Record Type: Journal Article
• Authors: Li, Yong‐Jiang; Zhang, Wen‐Jia; Zhan, Chen‐Lin; Chen, Ke‐Jie; Xue, Chun‐Dong; Wang, Yu; Chen, Xiao‐Ming; Qin, Kai‐Rong
• Editors: Xuan, Xiangchun; Yang, Chun
• Is Part Of: Electrophoresis. Volume 42:Issue 21/22(2021)
• Page Start: 2264
• Page End: 2272
• Publication Date: 2021-07-29
• Subjects: Autonomously oscillatory flow -- Cellular microenvironment -- Dynamic biochemical signals -- Dynamic shear stress -- Microfluidic chip; Electrophoresis -- Periodicals; Electrophoresis -- Periodicals; 541.372
• DOI: 10.1002/elps.202100128
• Languages: English
• ISSNs: 0173-0835

Abstract

Abstract: Biological cells in vivo typically reside in a dynamic flowing microenvironment with extensive biomechanical and biochemical cues varying in time and space. These dynamic biomechanical and biochemical signals together act to regulate cellular behaviors and functions. Microfluidic technology is an important experimental platform for mimicking extracellular flowing microenvironment in vitro . However, most existing microfluidic chips for generating dynamic shear stress and biochemical signals require expensive, large peripheral pumps and external control systems, unsuitable for being placed inside cell incubators to conduct cell biology experiments. This study has developed a microfluidic generator of dynamic shear stress and biochemical signals based on autonomously oscillatory flow. Further, based on the lumped‐parameter and distributed‐parameter models of multiscale fluid dynamics, the oscillatory flow field and the concentration field of biochemical factors has been simulated at the cell culture region within the designed microfluidic chip. Using the constructed experimental system, the feasibility of the designed microfluidic chip has been validated by simulating biochemical factors with red dye. The simulation results demonstrate that dynamic shear stress and biochemical signals with adjustable period and amplitude can be generated at the cell culture chamber within the microfluidic chip. The amplitudes of dynamic shear stress and biochemical signals is proportional to the pressure difference and inversely proportional to the flow resistance, while their periods are correlated positively with the flow capacity and the flow resistance. The experimental results reveal the feasibility of the designed microfluidic chip. Conclusively, the proposed microfluidic generator based on autonomously oscillatory flow can generate dynamic shear stress and biochemical signals without peripheral pumps and external control systems. In addition to reducing the experimental cost, due to the tiny volume, it is beneficial to be integrated into cell incubators for cell biology experiments. Thus, the proposed microfluidic chip provides a novel experimental platform for cell biology investigations.