Department of Mechanical Engineering, University of Melbourne, VIC 3010, Australia.
The Australian Centre for Blood Diseases, Monash University, 99 Commercial Road, Melbourne, VIC 3004, Australia.
Lab Chip. 2023 Jun 28;23(13):3092-3105. doi: 10.1039/d3lc00256j.
Hydrodynamic trapping of a particle or cluster of particles based on contact and non-contact approaches has brought prominent insights to micro-nano scale applications. Of the non-contact methods, image-based real-time control in cross-slot microfluidic devices is one of the most promising potential platform for single cellular assays. Here, we report results from experiments conducted in two cross-slot microfluidic channels of different widths, with varying real-time delay of the control algorithm and different magnification. Sustained trapping of 5 μm diameter particles was achieved with high strain rates, of order 10 s, higher than in any previous studies. Our experiments show that the maximum attainable strain rate is a function of the real-time delay of the control algorithm and the particle resolution (pixel/μm). Therefore, we anticipate that with further reduced time delays and enhanced particle resolution, considerably higher strain rates can be attained, opening the platform to single cellular assay studies where very high strain rates are required.
基于接触和非接触方法的流体动力学捕获颗粒或颗粒簇,为微纳尺度应用带来了显著的启示。在非接触方法中,基于交叉狭缝微流控装置的基于图像的实时控制是单细胞分析最有前途的潜在平台之一。在这里,我们报告了在两个不同宽度的交叉狭缝微流控通道中进行的实验结果,控制算法的实时延迟和放大倍数不同。以高于以往任何研究的高应变速率(约 10 s-1)实现了对 5 μm 直径颗粒的持续捕获。我们的实验表明,最大可达到的应变速率是控制算法的实时延迟和颗粒分辨率(像素/μm)的函数。因此,我们预计,随着进一步降低时间延迟和增强颗粒分辨率,可以实现更高的应变速率,从而为需要非常高应变速率的单细胞分析研究打开平台。