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Improved single-cell culture achieved using micromolding in capillaries technology coupled with poly (HEMA)

机译:使用毛细管中的微成型技术结合聚(HEMA)可以实现改进的单细胞培养

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摘要

Cell studies at the single-cell level are becoming more and more critical for understanding the complex biological processes. Here, we present an optimization study investigating the positioning of single cells using micromolding in capillaries technology coupled with the cytophobic biomaterial poly (2-hydroxyethyl methacrylate) (poly (HEMA)). As a cytophobic biomaterial, poly (HEMA) was used to inhibit cells, whereas the glass was used as the substrate to provide a cell adhesive background. The poly (HEMA) chemical barrier was obtained using micromolding in capillaries, and the microchannel networks used for capillarity were easily achieved by reversibly bonding the polydimethylsiloxane mold and the glass. Finally, discrete cell adhesion regions were presented on the glass surface. This method is facile and low cost, and the reagents are commercially available. We validated the cytophobic abilities of the poly (HEMA), optimized the channel parameters for higher quality and more stable poly (HEMA) patterns by investigating the effects of changing the aspect ratio and the width of the microchannel on the poly (HEMA) grid pattern, and improved the single-cell occupancy by optimizing the dimensions of the cell adhesion regions.
机译:为了了解复杂的生物过程,单细胞水平的细胞研究变得越来越重要。在这里,我们提出了一项优化研究,该研究利用毛细管技术中的微成型技术结合憎细胞生物材料聚(甲基丙烯酸2-羟乙酯)(聚(HEMA))来研究单个细胞的定位。聚(HEMA)作为憎细胞生物材料被用来抑制细胞,而玻璃被用作底物以提供细胞粘附背景。聚(HEMA)化学屏障是通过在毛细管中进行微成型而获得的,用于毛细管现象的微通道网络可通过将聚二甲基硅氧烷模具和玻璃可逆地结合而轻松实现。最后,在玻璃表面上出现了离散的细胞粘附区域。该方法简便且成本低廉,试剂可商购。我们通过研究改变长宽比和微通道宽度对聚(HEMA)网格图案的影响,验证了聚(HEMA)的疏水性,优化了通道参数以获得更高质量和更稳定的聚(HEMA)模式,并通过优化单元格粘附区域的尺寸来改善单细胞占用率。

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