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将芯片实验室胚胎技术与高清成像细胞术相结合。

Interfacing Lab-on-a-Chip Embryo Technology with High-Definition Imaging Cytometry.

作者信息

Zhu Feng, Hall Christopher J, Crosier Philip S, Wlodkowic Donald

机构信息

1 The BioMEMS Research Group, School of Applied Sciences, RMIT University , Victoria, Australia .

2 Department of Molecular Medicine and Pathology, University of Auckland , Auckland, New Zealand .

出版信息

Zebrafish. 2015 Aug;12(4):315-8. doi: 10.1089/zeb.2015.1105. Epub 2015 Jul 1.

Abstract

To spearhead deployment of zebrafish embryo biotests in large-scale drug discovery studies, automated platforms are needed to integrate embryo in-test positioning and immobilization (suitable for high-content imaging) with fluidic modules for continuous drug and medium delivery under microperfusion to developing embryos. In this work, we present an innovative design of a high-throughput three-dimensional (3D) microfluidic chip-based device for automated immobilization and culture and time-lapse imaging of developing zebrafish embryos under continuous microperfusion. The 3D Lab-on-a-Chip array was fabricated in poly(methyl methacrylate) (PMMA) transparent thermoplastic using infrared laser micromachining, while the off-chip interfaces were fabricated using additive manufacturing processes (fused deposition modelling and stereolithography). The system's design facilitated rapid loading and immobilization of a large number of embryos in predefined clusters of traps during continuous microperfusion of drugs/toxins. It was conceptually designed to seamlessly interface with both upright and inverted fluorescent imaging systems and also to directly interface with conventional microtiter plate readers that accept 96-well plates. Compared with the conventional Petri dish assays, the chip-based bioassay was much more convenient and efficient as only small amounts of drug solutions were required for the whole perfusion system running continuously over 72 h. Embryos were spatially separated in the traps that assisted tracing single embryos, preventing interembryo contamination and improving imaging accessibility.

摘要

为了在大规模药物发现研究中率先部署斑马鱼胚胎生物测试,需要自动化平台将胚胎在测试中的定位和固定(适用于高内涵成像)与流体模块集成,以便在微灌注下向发育中的胚胎持续输送药物和培养基。在这项工作中,我们展示了一种基于高通量三维(3D)微流控芯片的创新设计装置,用于在连续微灌注下对发育中的斑马鱼胚胎进行自动固定、培养和延时成像。3D芯片实验室阵列是使用红外激光微加工技术在聚甲基丙烯酸甲酯(PMMA)透明热塑性塑料中制造的,而芯片外接口则使用增材制造工艺(熔融沉积建模和立体光刻)制造。该系统的设计便于在药物/毒素连续微灌注过程中,将大量胚胎快速加载并固定在预定义的陷阱簇中。它在概念上设计为可与正置和倒置荧光成像系统无缝对接,还能直接与接受96孔板的传统微孔板读数器对接。与传统的培养皿检测相比,基于芯片的生物检测更加方便高效,因为整个灌注系统连续运行72小时仅需少量药物溶液。胚胎在陷阱中空间分离,有助于追踪单个胚胎,防止胚胎间污染并提高成像可达性。

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