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A novel dual-well array chip for efficiently trapping single-cell in large isolated micro-well without complicated accessory equipment

机译:一种新颖的双孔阵列芯片无需复杂的附属设备即可有效地捕获大型孤立微孔中的单细胞

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摘要

Conventional cell-sized well arrays have advantages of high occupancy, simple operation, and low cost for capturing single-cells. However, they have insufficient space for including reagents required for cell treatment or analysis, which restricts the wide application of cell-sized well arrays as a single-cell research tool alone. Here, we present a novel dual-well array chip, which integrates capture-wells (20 μm in diameter) with reaction-wells (100 μm in diameter) and describe a flow method for convenient single-cell analysis requiring neither complicated infra-structure nor high expenditure, while enabling highly efficient single cell trapping (75.8%) with only 11.3% multi-cells. Briefly, the cells are first loaded into the dual-wells by gravity and then multi-cells in the reaction-wells are washed out by phosphate buffer saline. Next, biochemical reagents are loaded into reaction-wells using the scraping method and the chip is packed as a sandwich structure. We thereby successfully measured intracellular β-galactosidase activity of K562 cells at the single-cell level. We also used computational simulations to illustrate the working principle of dual-well structure and found out a relationship between the wall shear stress distribution and the aspect ratio of the dual-well array chip which provides theoretical guidance for designing multi-wells chip for convenient single-cell analysis. Our work produced the first dual-well chip that can simultaneously provide a high occupancy rate for single cells and sufficient space for reagents, as well as being low in cost and simple to operate. We believe that the feasibility and convenience of our method will enhance its use as a practical single-cell research tool.
机译:常规细胞大小的孔阵列具有占用率高,操作简单和捕获单细胞成本低的优点。但是,它们没有足够的空间来容纳细胞处理或分析所需的试剂,这限制了细胞大小的孔阵列仅作为单细胞研究工具的广泛应用。在这里,我们介绍了一种新型的双孔阵列芯片,该芯片将捕获孔(直径为20μm)与反应孔(直径为100μm)集成在一起,并描述了一种方便的单细胞分析方法,不需要复杂的基础结构费用也不高,而仅用11.3%的多电池就可以实现高效的单细胞捕获(75.8%)。简而言之,首先通过重力将细胞加载到双孔中,然后用磷酸盐缓冲液将反​​应孔中的多细胞洗掉。接下来,使用刮擦法将​​生化试剂加载到反应孔中,并将芯片包装为三明治结构。因此,我们成功地在单细胞水平上测量了K562细胞的细胞内β-半乳糖苷酶活性。我们还通过计算仿真来说明双孔结构的工作原理,并发现壁切应力分布与双孔阵列芯片的长宽比之间的关系,这为方便单井设计多孔芯片提供了理论指导。细胞分析。我们的工作生产出了第一款双孔芯片,该芯片可同时提供单个细胞的高占用率和足够的试剂空间,并且成本低廉且易于操作。我们相信我们方法的可行性和便利性将增强其作为实用的单细胞研究工具的使用。

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