4.3 Article

Microfluidic Device for a Rapid Immobilization of Zebrafish Larvae in Environmental Scanning Electron Microscopy

期刊

CYTOMETRY PART A
卷 87A, 期 3, 页码 190-194

出版社

WILEY-BLACKWELL
DOI: 10.1002/cyto.a.22603

关键词

Danio rerio; environmental scanning electron microscopy; imaging; immobilization; lab-on-a-chip; larvae; microfluidics; Zebrafish

资金

  1. Australian Research Council DECRA [DE130101046]

向作者/读者索取更多资源

Small vertebrate model organisms have recently gained popularity as attractive experimental models that enhance our understanding of human tissue and organ development. Despite a large body of evidence using optical spectroscopy for the characterization of small model organism on chip-based devices, no attempts have been so far made to interface microfabricated technologies with environmental scanning electron microscopy (ESEM). Conventional scanning electron microscopy requires high vacuum environments and biological samples must be, therefore, submitted to many preparative procedures to dehydrate, fix, and subsequently stain the sample with gold-palladium deposition. This process is inherently low-throughput and can introduce many analytical artifacts. This work describes a proof-of-concept microfluidic chip-based system for immobilizing zebrafish larvae for ESEM imaging that is performed in a gaseous atmosphere, under low vacuum mode and without any need for sample staining protocols. The microfabricated technology provides a user-friendly and simple interface to perform ESEM imaging on zebrafish larvae. Presented lab-on-a-chip device was fabricated using a high-speed infrared laser micromachining in a biocompatible poly(methyl methacrylate) thermoplastic. It consisted of a reservoir with multiple semispherical microwells designed to hold the yolk of dechorionated zebrafish larvae. Immobilization of the larvae was achieved by a gentle suction generated during blotting of the medium. Trapping region allowed for multiple specimens to be conveniently positioned on the chip-based device within few minutes for ESEM imaging. (c) 2014 International Society for Advancement of Cytometry

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