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Integrated Microfluidic Device for Drug Studies of Early C. Elegans Embryogenesis

机译:集成的微流控装置用于早期线虫胚胎发生的药物研究

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摘要

Small molecules inhibitors are powerful tools for studying multiple aspects of cell biology and stand at the forefront of drug discovery pipelines. However, in the early Caenorhabditis elegans (C. elegans) embryo, which is a powerful model system for cell and developmental biology, the use of small molecule inhibitors has been limited by the impermeability of the embryonic eggshell, the low‐throughput manual embryo isolation methods, and the lack of well‐controlled drug delivery protocols. This work reports a fully integrated microfluidic approach for studies of C. elegans early embryogenesis, including the possibility of testing small molecule inhibitors with increased throughput and versatility. The setup enables robust on‐chip extraction of embryos from gravid adult worms in a dedicated pillar array chamber by mechanical compression, followed by rapid fluidic transfer of embryos into an adjacent microtrap array. Parallel analysis of ≈100 embryos by high‐resolution time‐lapse imaging from the one‐cell stage zygote until hatching can be performed with this device. The implementation of versatile microfluidic protocols, in particular time‐controlled and reversible drug delivery to on‐chip immobilized embryos, demonstrates the potential of the device for biochemical and pharmacological assays.
机译:小分子抑制剂是研究细胞生物学多个方面的有力工具,并且处于药物开发流程的最前沿。然而,在秀丽的秀丽隐杆线虫(C. elegans)早期胚胎中,它是细胞和发育生物学的强大模型系统,由于胚胎卵壳的不渗透性,低通量手工胚胎分离,限制了小分子抑制剂的使用。方法,以及缺乏良好控制的药物输送方案。这项工作报告了一种完全整合的微流控方法,用于研究秀丽隐杆线虫的早期胚胎发生,包括测试具有增加的通量和多功能性的小分子抑制剂的可能性。该设置可通过机械压缩从专用的柱状阵列腔室中从妊娠成年蠕虫中可靠地从芯片上提取胚胎,然后将胚胎快速流体转移到相邻的微阱阵列中。从单细胞阶段受精卵直至孵化的高分辨率延时成像可以并行分析约100个胚胎。通用微流控方案的实施,特别是将时间控制和可逆药物递送至固定在芯片上的胚胎,证明了该设备在生化和药理学检测中的潜力。

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