Literature DB >> 18989441

A microfluidic device with groove patterns for studying cellular behavior.

Bong Geun Chung1, Amir Manbachi, Ali Khademhosseini.   

Abstract

We describe a microfluidic device with microgrooved patterns for studying cellular behavior. This microfluidic platform consists of a top fluidic channel and a bottom microgrooved substrate. To fabricate the microgrooved channels, a top poly(dimethylsiloxane) (PDMS) mold containing the impression of the microfluidic channels was aligned and bonded to a microgrooved substrate. Using this device, mouse fibroblast cells were immobilized and patterned within microgrooved substrates (25, 50, 75, and 100 microm wide). To study apoptosis in a microfluidic device, media containing hydrogen peroxide, Annexin V, and propidium iodide was perfused into the fluidic channel for 2 hours. We found that cells exposed to the oxidative stress became apoptotic. These apoptotic cells were confirmed by Annexin V that bound to phosphatidylserine at the outer leaflet of the plasma membrane during the apoptosis process. Using this microfluidic device with microgrooved patterns, the apoptosis process was observed in real-time and analyzed by using an inverted microscope containing an incubation chamber (37 degrees C, 5% CO(2)). Therefore, this microfluidic device incorporated with microgrooved substrates could be useful for studying the cellular behavior and performing high-throughput drug screening.

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Year:  2007        PMID: 18989441      PMCID: PMC2565858          DOI: 10.3791/270

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  3 in total

1.  Cell docking inside microwells within reversibly sealed microfluidic channels for fabricating multiphenotype cell arrays.

Authors:  Ali Khademhosseini; Judy Yeh; George Eng; Jeffrey Karp; Hirokazu Kaji; Jeffrey Borenstein; Omid C Farokhzad; Robert Langer
Journal:  Lab Chip       Date:  2005-10-13       Impact factor: 6.799

2.  A detailed analysis of hydrogen peroxide-induced cell death in primary neuronal culture.

Authors:  E R Whittemore; D T Loo; J A Watt; C W Cotman
Journal:  Neuroscience       Date:  1995-08       Impact factor: 3.590

3.  A hybrid microfluidic-vacuum device for direct interfacing with conventional cell culture methods.

Authors:  Bong Geun Chung; Jeong Won Park; Jia Sheng Hu; Carlos Huang; Edwin S Monuki; Noo Li Jeon
Journal:  BMC Biotechnol       Date:  2007-09-20       Impact factor: 2.563

  3 in total
  1 in total

1.  Time-resolved, single-cell analysis of induced and programmed cell death via non-invasive propidium iodide and counterstain perfusion.

Authors:  Christina E M Krämer; Wolfgang Wiechert; Dietrich Kohlheyer
Journal:  Sci Rep       Date:  2016-09-01       Impact factor: 4.379

  1 in total

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