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A Bubble-Free Microfluidic Device for Easy-to-Operate Immobilization, Culturing and Monitoring of Zebrafish Embryos

机译:无气泡微流控设备,易于操作,固定和培养斑马鱼胚胎

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摘要

The development of miniaturized devices for studying zebrafish embryos has been limited due to complicated fabrication and operation processes. Here, we reported on a microfluidic device that enabled the capture and culture of zebrafish embryos and real-time monitoring of dynamic embryonic development. The device was simply fabricated by bonding two layers of polydimethylsiloxane (PDMS) structures replicated from three-dimensional (3D) printed reusable molds onto a flat glass substrate. Embryos were easily loaded into the device with a pipette, docked in traps by gravity, and then retained in traps with hydrodynamic forces for long-term culturing. A degassing chamber bonded on top was used to remove air bubbles from the embryo-culturing channel and traps so that any embryo movement caused by air bubbles was eliminated during live imaging. Computational fluid dynamics simulations suggested this embryo-trapping and -retention regime to exert low shear stress on the immobilized embryos. Monitoring of the zebrafish embryogenesis over 20 h during the early stages successfully verified the performance of the microfluidic device for culturing the immobilized zebrafish embryos. Therefore, this rapid-prototyping, low-cost and easy-to-operate microfluidic device offers a promising platform for the long-term culturing of immobilized zebrafish embryos under continuous medium perfusion and the high-quality screening of the developmental dynamics.
机译:由于复杂的制造和操作过程,用于研究斑马鱼胚胎的小型设备的开发受到了限制。在这里,我们报道了一种微流体设备,该设备能够捕获和培养斑马鱼胚胎,并实时监控动态胚胎发育。通过将两层从三维(3D)打印的可重复使用模具复制的聚二甲基硅氧烷(PDMS)结构粘合到平面玻璃基板上,可以简单地制造该设备。胚胎很容易用移液器装载到设备中,靠重力固定在陷阱中,然后利用流体动力将其保留在陷阱中以进行长期培养。顶部的脱气室用于去除胚胎培养通道和捕集阱中的气泡,以便在实时成像过程中消除由气泡引起的任何胚胎运动。计算流体动力学模拟表明,这种胚胎捕获和保留机制可以在固定的胚胎上施加低剪切应力。在早期阶段对斑马鱼胚胎发生的20多个小时的监测成功验证了用于固定化斑马鱼胚胎培养的微流控设备的性能。因此,这种快速成型,低成本和易于操作的微流体装置为在连续培养基灌注下长期培养固定化斑马鱼胚胎和高质量筛选发育动力学提供了有希望的平台。

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