Sun Xiange, Li Bowen, Li Wenman, Ren Xiaodong, Su Ning, Li Ruoxu, Li Jinmi, Huang Qing
Department of Laboratory Medicine, Daping Hospital, Army Medical University, Chongqing 400042, China.
Micromachines (Basel). 2022 Aug 7;13(8):1272. doi: 10.3390/mi13081272.
Microchips are fundamental tools for single-cell analysis. Although various microfluidic methods have been developed for single-cell trapping and analysis, most microchips cannot trap single cells deterministically for further analysis. In this paper, we describe a novel resistance-based microfluidic chip to implement deterministic single-cell trapping followed by immunofluorescence staining based on the least flow resistance principle. The design of a large circular structure before the constriction and the serpentine structure of the main channel made the flow resistance of the main channel higher than that of the trapping channel. Since cells preferred to follow paths with lower flow resistance, this design directed cells into the capture sites and improved single-cell trapping efficiency. We optimized the geometric parameters using numerical simulations. Experiments using A549 and K562 cell lines demonstrated the capability of our chip with (82.7 ± 2.4)% and (84 ± 3.3)% single-cell trapping efficiency, respectively. In addition, cells were immobilized at capture sites by applying the pulling forces at the outlet, which reduced the cell movement and loss and facilitated tracking of the cell in real time during the multistep immunofluorescence staining procedure. Due to the simple operation, high-efficiency single-cell trapping and lower cell loss, the proposed chip is expected to be a potential analytical platform for single tumor cell heterogeneity studies and clinical diagnosis.
微芯片是单细胞分析的基础工具。尽管已经开发出各种用于单细胞捕获和分析的微流控方法,但大多数微芯片无法确定性地捕获单个细胞以进行进一步分析。在本文中,我们描述了一种新型的基于电阻的微流控芯片,该芯片基于最小流阻原理实现确定性单细胞捕获,随后进行免疫荧光染色。收缩段之前的大圆形结构和主通道的蛇形结构设计使得主通道的流阻高于捕获通道的流阻。由于细胞倾向于沿着流阻较低的路径移动,这种设计将细胞引导至捕获位点并提高了单细胞捕获效率。我们使用数值模拟优化了几何参数。使用A549和K562细胞系进行的实验表明,我们的芯片单细胞捕获效率分别为(82.7 ± 2.4)%和(84 ± 3.3)%。此外,通过在出口处施加拉力将细胞固定在捕获位点,这减少了细胞移动和损失,并便于在多步免疫荧光染色过程中实时跟踪细胞。由于操作简单、单细胞捕获效率高且细胞损失低,所提出的芯片有望成为用于单个肿瘤细胞异质性研究和临床诊断的潜在分析平台。