McClean: Flow Cells - Revision history

Megan N McClean: /* Notes */

2012-08-13T22:42:11Z

Notes

←Older revision		Revision as of 22:42, 13 August 2012
Line 69:		Line 69:
	#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.		#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
	#Anecdotal observations that might be of use to others can also be posted here.		#Anecdotal observations that might be of use to others can also be posted here.
		+
		+	*[[User:Megan N McClean\|Megan N McClean]] 18:42, 13 August 2012 (EDT) Running the plasma for longer will '''NOT''' give you better bonding. The surface of the PDMS will become glassy and no longer stick to the glass. Don't got much over 5 seconds for plasma cleaning your chip.
		+

	Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.		Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.

Megan N McClean: /* Protocol */

2012-08-13T22:41:08Z

Protocol

←Older revision		Revision as of 22:41, 13 August 2012
Line 25:		Line 25:

	==Protocol==		==Protocol==
-		+	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. Don't get uncured PDMS onto cured chips, as this will prevent the chips from properly bonding to the glass coverslip. In practive this means you should use one pair of gloves for mixing the PDMS and another, clean pair for cutting out the chips and bonding them to the coverslip.
-	~~===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====		====Mixing PDMS to fill the mold====
Line 45:		Line 43:
	====Cutting out the Chip====		====Cutting out the Chip====
	# 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.		# 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.
-	# 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.	+	# 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. When you have cut out your chip, cover the channel side with scotch tape.
	====Punch inlet and outlet ports in your chip====		====Punch inlet and outlet ports in your chip====
	=====Blunt Needle Technique=====		=====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.~~	+	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.
	=====Biopsy Punch Technique=====		=====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.~~	+	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.
-		+
-		+
-		+

		+	====Plasma bonding the PDMS chip to the coverslip====
		+	# Clean the channel side of the chip using scotch tape. Press and remove scotch tape 3X’s from the channel side of the chip.
		+	# Turn on the vacumn pump to the plasma preen (leftmost switch labelled "Vacumn Pump Power"). You will hear the vacumn pump at your feet turn on
		+	# Remove the glass chamber. Be careful of the two glass balls on the bottom of the chamber, they tend to catch and the whole chamber can get stuck!
		+	# Place your chip (tape free) and a glass coverslip inside. Make sure that the PDMS chip is channel-side up.
		+	# Replace the glass chamber and close the microwave door.
		+	# Turn on the air flow (middle switch labelled "Gas Control") and the vacumn (rightmost switch labeled "System Vacuum")
		+	# Wait about 20 seconds and then adjust the leftmost gas control to be at about 2
		+	# Hit "1" on the microwave pannel. The microwave will start. When you see pink/purple plasma, count to 5, and then hit "Cancel/Off"
		+	# Turn off the Gas Control and the System Vacuum.
		+	# Remove the chip and glass coverslip, and put the PDMS channel-side down on the glass (onto the side of the glass that was facing up). You should see the PDMS bond to the glass.
		+	# For extra bonding, bake the chip in the oven at 65°C for a few hours or overnight.

	==Notes==		==Notes==

Megan N McClean at 22:31, 13 August 2012

2012-08-13T22:31:08Z

←Older revision		Revision as of 22:31, 13 August 2012
Line 2:		Line 2:

	==Overview==		==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 ~~mask~~ that already has your desired pattern on it. We make out own ~~masks~~ in the [[http://www.princeton.edu/microfluidics/\| Princeton Microfluidics Laboratory]]	+	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 [http://www.princeton.edu/microfluidics/index.xls\| Princeton Microfluidics Laboratory].

	==Materials==		==Materials==
-	* Slygard	+	* Slygard 184 Silicon Elastromer (Ellsworth Adhesives)
-	• 4” petri dishes (for storing chips)	+	* 4” petri dishes (for storing chips)
-	~~• small~~ ~6” pieces of the intramedic tubing (ID 0.86mm OD 1.27mm)	+	* Small ~6” pieces of the intramedic tubing (ID 0.86mm OD 1.27mm)
-	~~• razor~~ blades	+	* Razor blades
-	~~• Nitrile gloves~~	+	* Biopsy Punches (1.2mm, 1.0mm, 0.75mm diameters) (
-	• Biopsy Punches (1.2mm, 1.0mm, 0.75mm diameters)	+	* Nitrile gloves
-	• Stainless steel blunt needle, 16 ½” gauge	+	* Stainless steel blunt needle, 16 ½” gauge
-	• Small green needle (21 ½ gauge Becton-Dickinson)	+	* Small green needle (21 ½ gauge Becton-Dickinson)
-	~~• Pieces of scrap PDMS (in small petri dishes on your bench)~~	+	* Scotch tape
-	~~• Cured PDMS, cut from molds (in 4” petri dishes, covered with tape)~~	+	* 1ml syringes with Luer-Lok tips
-	• Scotch tape	+	* 1.5mm Coverslips
-	• 1ml syringes with Luer-Lok tips	+	* Oven set to 65°C
-	~~• 4” petri dishes~~	+	* TMCS (chlorotrimethyl silane)
-	~~• 4” silicon wafers~~	+	* plastic forks for mixing PDMS
-	~~• SU8-20205 photoresist~~	+	* plastic beakers for mixing PDMS
-	~~• SU8 developer (propylene glycol monomethyl ether acetate PGMEA)~~	+	* Vacumn jar for degassing PDMS
-	~~• Transparency Masks~~	+
-	~~• Wafer Tweezers~~	+
-	~~• Scotch tape~~	+
-	~~• Scissors~~	+
-	~~• Transparency Masks~~	+
-	~~• Aluminum foil~~	+
-	~~• Acetone~~	+
-	~~• Cleanroom wipes (do not shed particles like paper towels or Kim wipes)~~	+
-	~~• HMDS (hexamethyldisilazane)~~	+
-	~~• 5” square glass plates with rounded edges~~	+
-	~~• Lab coat~~	+
-	~~• Hairnets~~	+
-	~~• nitrile glocse~~	+
-	~~• Cleanroom booties~~	+
-	~~• Safety glasses~~	+
-	~~• Sheet protectors for holding protocols~~	+
-	~~• Cleanroom paper for taking notes~~	+
-	~~• Timers~~	+
-	~~• Slygard 184 Silicon Elastromer~~	+
-	~~• Rough PDMS chips cut from molds~~	+
-	• 1.5mm Coverslips	+
-	• Oven set to 65°C ~~(Microarray hybridization oven)~~	+
-	~~• Scotch tape~~	+
-	~~• Nitrile gloves~~	+
-	• TMCS (chlorotrimethyl silane)	+
-	• plastic forks for mixing PDMS	+
-	• plastic beakers for mixing PDMS	+
-	• Vacumn jar for degassing PDMS	+
-	~~• Microfluidic chips constructed previously~~	+
-	~~• Tubing~~	+
-	~~• Microscopes~~	+
-	~~• Fluoresceine solution in water~~	+
-	~~• rhodamine solution in water~~	+
-	~~• 15ml conical tubes~~	+
-	~~• Syringes with tubing for injecting the chips.~~	+
-	~~• 70% ethanol in a 50ml conical~~	+
-	~~• Deionized water in a 50ml conical~~	+


Line 64:		Line 27:

	===Mixing the PDMS===		===Mixing the PDMS===
-	~~Today you will start with your silicon wafer.~~ 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.	+	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====
		+	# 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
		+	# For these molds you will need ~60 g of total solution the first time you fill up the petri dish (assuming a 4" dish).
		+	# 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====
		+	# 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.
		+	# 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.
		+	# 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====
		+	# Pour the PDMS carefully into your mold, trying hard not to introduce bubbles that you have worked so hard to eliminate.
		+	# If you do introduce bubbles carefully use a 21G 1 1/2 gauge needle to move them to the side.
		+	====Curing the PDMS====
		+	# 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====
		+	# 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.
		+	# 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==		==Notes==

Megan N McClean at 22:18, 13 August 2012

2012-08-13T22:18:38Z

←Older revision		Revision as of 22:18, 13 August 2012
Line 2:		Line 2:

	==Overview==		==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 mask that already has your desired pattern on it. We make out own masks in the [[~~Princeton Microfluidics Laboratory \|~~ http://www.princeton.edu/microfluidics/ ]]	+	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 mask that already has your desired pattern on it. We make out own masks in the [[http://www.princeton.edu/microfluidics/\| Princeton Microfluidics Laboratory]]

	==Materials==		==Materials==

Megan N McClean at 22:18, 13 August 2012

2012-08-13T22:18:12Z

←Older revision		Revision as of 22:18, 13 August 2012
Line 2:		Line 2:

	==Overview==		==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 mask that already has your desired pattern on it. We make out own masks in the [Princeton Microfluidics Laboratory ]http://www.princeton.edu/microfluidics/	+	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 mask that already has your desired pattern on it. We make out own masks in the [[Princeton Microfluidics Laboratory \| http://www.princeton.edu/microfluidics/ ]]

	==Materials==		==Materials==

Megan N McClean at 22:17, 13 August 2012

2012-08-13T22:17:07Z

←Older revision		Revision as of 22:17, 13 August 2012
Line 2:		Line 2:

	==Overview==		==Overview==
-	This protocol covers the soft lithography and plasma bonding steps used to make flow cells out of PDMS in our lab.	+	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 mask that already has your desired pattern on it. We make out own masks in the [Princeton Microfluidics Laboratory ]http://www.princeton.edu/microfluidics/

	==Materials==		==Materials==
Line 64:		Line 64:

	===Mixing the PDMS===		===Mixing the PDMS===
-		+	Today you will start with your silicon wafer. 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.

	==Notes==		==Notes==

Megan N McClean: New page: ==Overview== This protocol covers the soft lithography and plasma bonding steps used to make flow cells out of PDMS in our ...

2012-08-13T22:15:02Z

New page:  ==Overview== This protocol covers the soft lithography and plasma bonding steps used to make flow cells out of PDMS in our ...

New page

==Overview==
This protocol covers the soft lithography and plasma bonding steps used to make flow cells out of PDMS in our lab.

==Materials==
* Slygard
• 4” petri dishes (for storing chips)
• small ~6” pieces of the intramedic tubing (ID 0.86mm OD 1.27mm)
• razor blades
• Nitrile gloves
• Biopsy Punches (1.2mm, 1.0mm, 0.75mm diameters)
• Stainless steel blunt needle, 16 ½” gauge
• Small green needle (21 ½ gauge Becton-Dickinson)
• Pieces of scrap PDMS (in small petri dishes on your bench)
• Cured PDMS, cut from molds (in 4” petri dishes, covered with tape)
• Scotch tape
• 1ml syringes with Luer-Lok tips
• 4” petri dishes
• 4” silicon wafers
• SU8-20205 photoresist
• SU8 developer (propylene glycol monomethyl ether acetate PGMEA)
• Transparency Masks
• Wafer Tweezers
• Scotch tape
• Scissors
• Transparency Masks
• Aluminum foil
• Acetone
• Cleanroom wipes (do not shed particles like paper towels or Kim wipes)
• HMDS (hexamethyldisilazane)
• 5” square glass plates with rounded edges
• Lab coat
• Hairnets
• nitrile glocse
• Cleanroom booties
• Safety glasses
• Sheet protectors for holding protocols
• Cleanroom paper for taking notes
• Timers
• Slygard 184 Silicon Elastromer
• Rough PDMS chips cut from molds
• 1.5mm Coverslips
• Oven set to 65°C (Microarray hybridization oven)
• Scotch tape
• Nitrile gloves
• TMCS (chlorotrimethyl silane)
• plastic forks for mixing PDMS
• plastic beakers for mixing PDMS
• Vacumn jar for degassing PDMS
• Microfluidic chips constructed previously
• Tubing
• Microscopes
• Fluoresceine solution in water
• rhodamine solution in water
• 15ml conical tubes
• Syringes with tubing for injecting the chips.
• 70% ethanol in a 50ml conical
• Deionized water in a 50ml conical

==Protocol==

===Mixing the PDMS===

==Notes==

Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!
#List troubleshooting tips here.
#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
#Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.

==References==

==Contact==

*'''[[User:Megan N McClean|Megan N McClean]] 14:01, 20 July 2011 (EDT)'''

or instead, [[Talk:{{PAGENAME}}|discuss this protocol]].


[[Category:Protocol]]