Literature DB >> 18989411

Brain slice stimulation using a microfluidic network and standard perfusion chamber.

Javeed Shaikh Mohammed1, Hugo Caicedo, Christopher P Fall, David T Eddington.   

Abstract

We have demonstrated the fabrication of a two-level microfluidic device that can be easily integrated with existing electrophysiology setups. The two-level microfluidic device is fabricated using a two-step standard negative resist lithography process. The first level contains microchannels with inlet and outlet ports at each end. The second level contains microscale circular holes located midway of the channel length and centered along with channel width. Passive pumping method is used to pump fluids from the inlet port to the outlet port. The microfluidic device is integrated with off-the-shelf perfusion chambers and allows seamless integration with the electrophysiology setup. The fluids introduced at the inlet ports flow through the microchannels towards the outlet ports and also escape through the circular openings located on top of the microchannels into the bath of the perfusion. Thus the bottom surface of the brain slice placed in the perfusion chamber bath and above the microfluidic device can be exposed with different neurotransmitters. The microscale thickness of the microfluidic device and the transparent nature of the materials [glass coverslip and PDMS (polydimethylsiloxane)] used to make the microfluidic device allow microscopy of the brain slice. The microfluidic device allows modulation (both spatial and temporal) of the chemical stimuli introduced to the brain slice microenvironments.

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Year:  2007        PMID: 18989411      PMCID: PMC2562487          DOI: 10.3791/302

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


  2 in total

1.  A passive pumping method for microfluidic devices.

Authors:  Glenn M Walker; David J Beebe
Journal:  Lab Chip       Date:  2002-08-05       Impact factor: 6.799

2.  Multilayer PDMS microfluidic chamber for controlling brain slice microenvironment.

Authors:  A J Blake; T M Pearce; N S Rao; S M Johnson; J C Williams
Journal:  Lab Chip       Date:  2007-05-24       Impact factor: 6.799

  2 in total
  3 in total

1.  User-defined local stimulation of live tissue through a movable microfluidic port.

Authors:  Megan A Catterton; Austin F Dunn; Rebecca R Pompano
Journal:  Lab Chip       Date:  2018-07-10       Impact factor: 6.799

2.  Spatially resolved microfluidic stimulation of lymphoid tissue ex vivo.

Authors:  Ashley E Ross; Maura C Belanger; Jacob F Woodroof; Rebecca R Pompano
Journal:  Analyst       Date:  2016-11-30       Impact factor: 4.616

3.  Fitting tissue chips and microphysiological systems into the grand scheme of medicine, biology, pharmacology, and toxicology.

Authors:  David E Watson; Rosemarie Hunziker; John P Wikswo
Journal:  Exp Biol Med (Maywood)       Date:  2017-10
  3 in total

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