McClean: Flow Cells

Overview

This protocol covers the soft lithography and plasma bonding steps used to make flow cells out of PDMS in our lab. This protocol assumes that you are starting with a silicon wafer mold that already has your desired pattern on it. We make out own SU8 molds in the Princeton Microfluidics Laboratory.

Materials

• Slygard 184 Silicon Elastromer (Ellsworth Adhesives)
• 4” petri dishes (for storing chips)
• Small ~6” pieces of the intramedic tubing (ID 0.86mm OD 1.27mm)
• Razor blades
• Biopsy Punches (1.2mm, 1.0mm, 0.75mm diameters) (
• Nitrile gloves
• Stainless steel blunt needle, 16 ½” gauge
• Small green needle (21 ½ gauge Becton-Dickinson)
• Scotch tape
• 1ml syringes with Luer-Lok tips
• 1.5mm Coverslips
• Oven set to 65°C
• TMCS (chlorotrimethyl silane)
• plastic forks for mixing PDMS
• plastic beakers for mixing PDMS
• Vacumn jar for degassing PDMS

Protocol

Mixing the PDMS

Wear nitrile gloves, as oils from your hands can prevent the PDMS from curing and/or bonding properly. Please try to not drip PDMS everywhere. It is extremely hard to clean up.

Mixing PDMS to fill the mold

1. Mix PDMS in a 1:9 ratio (by weight) curing agent to polymer in a plastic solo cup. The easiest way to do this is by weighing out the polymer first in the plastic solo cup on a balance and then adding the appropriate amount of curing agent
2. For these molds you will need ~60 g of total solution the first time you fill up the petri dish (assuming a 4" dish).
3. Mix the PDMS THOROUGHLY using a plastic fork. When you think that you’ve mixed it enough, mix it some more. Uneven mixing will lead to uneven curing of the PDMS.

Degassing the PDMS

1. Place your PDMS in the vacumn bell jar in the hood and turn on the vacumn. Please wait for your classmates because you will all need to be degassing PDMS at the same time.
2. Watch the PDMS degassing. If it looks like it is about to bubble over, release the vacumn, let the bubbles collapse, and then restart the vacumn. Keep an eye on it for at least 10 minutes.
3. Make sure that your PDMS is completely free of bubbles. The total degassing process will probably take 15 minutes. While you are waiting you may move on to testing the chips you made previously.

Pour the PDMS

1. Pour the PDMS carefully into your mold, trying hard not to introduce bubbles that you have worked so hard to eliminate.
2. If you do introduce bubbles carefully use a 21G 1 1/2 gauge needle to move them to the side.

Curing the PDMS

1. Cure the PDMS at 65°C until it is firm and not tacky at all. This will probably take an hour. You can also do this overnight if you are running out of time.

Cutting out the Chip

1. Using a razor blade, carefully cut around the mask components visible through the PDMS. DO NOT CUT YOURSELF. DO NOT under ANY circumstances push down on the underlying silicon wafer. This will crack the wafer rendering it useless for classmates and for future chip making. It is expensive to replace these molds, so BE GENTLE!!! The best way to cut out the PDMS is to gently circle, removing slightly more PDMS each time. When you see an air bubble form under the PDMS you are getting close, but DO NOT rush at this point. Carefully keep circling the groove until the chunk of PDMS pops-out.
2. Cut the large piece of PDMS into individual chips. You want each chip to fit onto your coverslip. Don't cut your chip too small, as this will give it less surface area with which to bond to the coverslip.

Punch inlet and outlet ports in your chip

Blunt Needle Technique

Place a piece of scrap PDMS flat on your bench and push a blunt needle through the PDMS. Then use a smaller 21 G 1 ½ needle (pointed) to remove the plug of PDMS from the end of the blunt needle before pulling the blunt needle back through the PDMS to leave a port. Ask the course staff if you need a demonstration.

Biopsy Punch Technique

Put a piece of scrap PDMS flat on your bench and use a biopsy punch to push through the PDMS. Be very careful to punch strain down and please don’t bend the tip of the biopsy punch (this renders them basically useless). Eject the plug of PDMS before pulling the biopsy punch back through the PDMS to leave a hole. Ask the course staff if you need a demonstration.

Notes

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!

1. List troubleshooting tips here.
2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
3. Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.

Contact

• Megan N McClean 14:01, 20 July 2011 (EDT)

or instead, discuss this protocol.