Difference between revisions of "Team:Pasteur Paris/Experiments"

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     <h2 style="order:1">Microfluidics</h2>
 
     <h2 style="order:1">Microfluidics</h2>
  
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     <p style="text-indent:0px;order:2;">PDMS (Polydimethylsiloxane) is a widely used polymer in microfluidics, for its biocompatibility and transparence, among other qualities. Here we show how to prepare PDMS for microfluidic chips, as well as how to demold them, bond them to other surfaces and treat them for neuron growth. Also, we explain how our molds and chips were fabricated.</p>                          
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     <p style="text-indent:0px;order:2;">PDMS (Polydimethylsiloxane) is a widely used polymer in microfluidics, for its biocompatibility and transparence, among other qualities. Here we show how to prepare PDMS for microfluidic chips, as well as how to demold them, bond them to other surfaces and treat them for neuron growth. Also, we explain how our molds and chips were fabricated.</p>                        
  
  
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         <h3>Protocol</h3>
 
         <h3>Protocol</h3>
 
         <br>
 
         <br>
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         <ul>
 
         <ul>
 
             <li> Pour poly-D-lysine with concentration 10 &mu g/mL into the chip  </li>
 
             <li> Pour poly-D-lysine with concentration 10 &mu g/mL into the chip  </li>
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         </div>
 
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         <br>
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         <h3>Materials</h3>
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         <p> We were allowed to use the molds made by Institut Curie. We were not involved in the process of their fabrication. Here is a short video we made about how these molds were created </p>
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        <ul>
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            <li>  Poly-D-Lysine solution 1.0 mg/mL (Sigma aldrich, A-003-E)  </li>
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            <li>  Laminin (Sigma aldrich, Laminin from Engelbreth-Holm-Swarm murine sarcoma basement membrane, L2020-1MG) </li>
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        </ul>
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         <br>
 
         <br>
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         <h3>Protocol</h3>
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         <video width="640" height="360" controls>
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        <br>
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             <source src="https://static.igem.org/mediawiki/2018/d/d1/T--Pasteur_Paris--Mold-Fabrication-iGEM.mp4" type="video/mp4">
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        <ul>
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        </video>
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             <li> Pour poly-D-lysine with concentration 10 &mu g/mL into the chip  </li>
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         <br>  
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            <li> Incubate over night </li>
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            <li> Pour laminine with concentration 4 &mu g/mL </li>
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            <li> Incubate for a few hours</li>
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        <br>
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        <div class="protocol_box">
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            <p> Get full protocol here </p>
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         </div>
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            <br>  
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         </div>
 
         </div>
 
     </div>   
 
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Revision as of 14:08, 17 August 2018

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PROTOCOLS

Microfluidics

PDMS (Polydimethylsiloxane) is a widely used polymer in microfluidics, for its biocompatibility and transparence, among other qualities. Here we show how to prepare PDMS for microfluidic chips, as well as how to demold them, bond them to other surfaces and treat them for neuron growth. Also, we explain how our molds and chips were fabricated.

PDMS Chips Fabrication

PDMS Chip Demolding

PDMS Chip Bonding

PDMS Chip Treatment for Nerve Growth

PDMS Microchannel Chip Mold Fabrication


Materials

  • Sylgard 184 Elastomer Kit (Sigma-aldrich, 761036-5EA)
  • Vacuum pump unit (Vacuubrand PC 3 RZ 2.5)
  • Stove (Memmert UM 400)

Protocol

According to manufacturer's instruction.

  • Mix monomer and curing agent (10:1 proportion) for 30 seconds
  • Use a vacuum pump unit and a vacuum bell jar to extract air bubbles until the mixture is clear
  • Pour mixture onto mold
  • Put mixture+mold in stove at 70 degrees Celsius for 3 hours

Get full protocol here



Materials

  • Razor blade (OEMTOOLS 25181 Razor Blades, 100 Pack)
  • Biopsy puncher (Kai Biopsy Punch 4mm )

Protocol


  • Cut the borders of the chip with the razor blade
  • Extract the chip from its mold
  • Drill input and output holes with the biopsy puncher

Get full protocol here



Materials

  • Plasma cleaner (Diener Pico PCCE)
  • Distilled water (Fisherbrand, CAS number 7732-18-5)
  • Isopropanol (Fisherbrand, CAS number 67-63-0)
  • Office duct tape
  • Vertical laminar airflow cabinets (Euroclone aura vertical S.D.4)

Protocol


  • Take chip and the surface it needs to be bonded to into the airflow cabinet
  • Clean chip with duct tape and isopropanol
  • Put the chip and the surface into the plasma cleaner.
  • Expose chip and surface 30 seconds to plasma.
  • Take the chip and the surface back in the airflow cabinet
  • Press the microfluidic chip against the surface
  • Insert distilled water into chip circuitry

    • Get full protocol here



Materials

  • Poly-D-Lysine solution 1.0 mg/mL (Sigma aldrich, A-003-E)
  • Laminin (Sigma aldrich, Laminin from Engelbreth-Holm-Swarm murine sarcoma basement membrane, L2020-1MG)

Protocol


  • Pour poly-D-lysine with concentration 10 &mu g/mL into the chip
  • Incubate over night
  • Pour laminine with concentration 4 &mu g/mL
  • Incubate for a few hours

    • Get full protocol here



We were allowed to use the molds made by Institut Curie. We were not involved in the process of their fabrication. Here is a short video we made about how these molds were created