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Miniaturized Embryo Array for Automated Trapping, Immobilization and Microperfusion of Zebrafish Embryos

Overview of attention for article published in PLOS ONE, May 2012
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Title
Miniaturized Embryo Array for Automated Trapping, Immobilization and Microperfusion of Zebrafish Embryos
Published in
PLOS ONE, May 2012
DOI 10.1371/journal.pone.0036630
Pubmed ID
Authors

Jin Akagi, Khashayar Khoshmanesh, Barbara Evans, Chris J. Hall, Kathryn E. Crosier, Jonathan M. Cooper, Philip S. Crosier, Donald Wlodkowic

Abstract

Zebrafish (Danio rerio) has recently emerged as a powerful experimental model in drug discovery and environmental toxicology. Drug discovery screens performed on zebrafish embryos mirror with a high level of accuracy the tests usually performed on mammalian animal models, and fish embryo toxicity assay (FET) is one of the most promising alternative approaches to acute ecotoxicity testing with adult fish. Notwithstanding this, automated in-situ analysis of zebrafish embryos is still deeply in its infancy. This is mostly due to the inherent limitations of conventional techniques and the fact that metazoan organisms are not easily susceptible to laboratory automation. In this work, we describe the development of an innovative miniaturized chip-based device for the in-situ analysis of zebrafish embryos. We present evidence that automatic, hydrodynamic positioning, trapping and long-term immobilization of single embryos inside the microfluidic chips can be combined with time-lapse imaging to provide real-time developmental analysis. Our platform, fabricated using biocompatible polymer molding technology, enables rapid trapping of embryos in low shear stress zones, uniform drug microperfusion and high-resolution imaging without the need of manual embryo handling at various developmental stages. The device provides a highly controllable fluidic microenvironment and post-analysis eleuthero-embryo stage recovery. Throughout the incubation, the position of individual embryos is registered. Importantly, we also for first time show that microfluidic embryo array technology can be effectively used for the analysis of anti-angiogenic compounds using transgenic zebrafish line (fli1a:EGFP). The work provides a new rationale for rapid and automated manipulation and analysis of developing zebrafish embryos at a large scale.

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Mendeley readers

The data shown below were compiled from readership statistics for 129 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 <1%
United States 1 <1%
Germany 1 <1%
France 1 <1%
Unknown 125 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 28 22%
Researcher 25 19%
Student > Master 16 12%
Student > Bachelor 12 9%
Other 8 6%
Other 17 13%
Unknown 23 18%
Readers by discipline Count As %
Engineering 31 24%
Agricultural and Biological Sciences 29 22%
Biochemistry, Genetics and Molecular Biology 12 9%
Chemistry 3 2%
Neuroscience 3 2%
Other 22 17%
Unknown 29 22%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 July 2015.
All research outputs
#17,670,096
of 22,684,168 outputs
Outputs from PLOS ONE
#146,273
of 193,651 outputs
Outputs of similar age
#121,987
of 163,917 outputs
Outputs of similar age from PLOS ONE
#2,844
of 3,792 outputs
Altmetric has tracked 22,684,168 research outputs across all sources so far. This one is in the 19th percentile – i.e., 19% of other outputs scored the same or lower than it.
So far Altmetric has tracked 193,651 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 15.0. This one is in the 20th percentile – i.e., 20% of its peers scored the same or lower than it.
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