Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan.
Lab Chip. 2019 May 14;19(10):1828-1837. doi: 10.1039/c9lc00053d.
Even though a number of microfluidic systems for particle/cell sorting have been proposed, facile and versatile platforms that provide sufficient sorting throughput and good operability are still under development. Here we present a simple but effective numbering-up strategy to dramatically increase the throughput of a continuous-flow particle/cell sorting scheme based on hydrodynamic filtration (HDF). A microfluidic channel equipped with multiple branches has been employed as a unit structure for size-based filtration, which realizes precise sorting without necessitating sheath flows. According to the concept of resistive circuit models, we designed and fabricated microdevices incorporating 64 or 128 closely assembled, multiplied units with a separation size of 5.0/7.0 μm. In proof-of-concept experiments, we successfully separated single micrometer-sized model particles and directly separated blood cells (erythrocytes and leukocytes) from blood samples. Additionally, we further increased the unit numbers by laminating multiple layers at a processing speed of up to 15 mL min-1. The presented numbering-up strategy would provide a valuable insight that is universally applicable to general microfluidic particle/cell sorters and may facilitate the actual use of microfluidic systems in biological studies and clinical diagnosis.
尽管已经提出了许多用于颗粒/细胞分选的微流控系统,但仍在开发便于使用且功能多样的平台,以提供足够的分选通量和良好的操作性。在这里,我们提出了一种简单而有效的扩展策略,可以大大提高基于流体动力学过滤 (HDF) 的连续流颗粒/细胞分选方案的通量。一个配备多个分支的微流道被用作基于尺寸的过滤的单元结构,它实现了精确的分选,而不需要鞘流。根据电阻电路模型的概念,我们设计并制造了微器件,其中包含 64 或 128 个紧密组装的、倍增单元,分离尺寸为 5.0/7.0 μm。在概念验证实验中,我们成功地分离了单个微米级的模型颗粒,并直接从血液样本中分离出血细胞(红细胞和白细胞)。此外,我们通过以高达 15 mL min-1 的处理速度分层多个层,进一步增加了单元数量。所提出的扩展策略将提供一个普遍适用于一般微流控颗粒/细胞分选器的有价值的见解,并可能促进微流控系统在生物研究和临床诊断中的实际应用。