Archive for June, 2010

Quick-connect tubing adapters with small dead volume

Gregory A Cooksey1 and Glynis Mattheisen2

1 Biochemical Science Division, National Institute of Standards and Technology, Gaithersburg, MD
2 Louisiana State University, Baton Rouge, LA

Why is this useful?


Luer adapters are convenient tools to rapidly and reversibly connect tubing from fluid reservoirs to microfluidic devices. One problem associated with the use of these adapters is that they trap considerable dead volume (approx 100 µl), which dramatically increases the time required to rinse away one fluid when another fluid is to be delivered down the same line. Another common shortcoming of leur adapters is that they are only available for 1.59 mm (1/16″) and larger inner diameter (ID) tubing. We demonstrate how to modify luer adapters to fit almost any size tubing while dramatically reducing the dead fluid volume trapped inside the connector.

What do I need?


  • 25 mm or longer needle or stainless steel tubing.  We use blunt 25 gauge needles (McMasterCarr # 75165A761). Use extreme care with exposed needles!
  • Polypropylene 1/16 in. barbed male luer adapter (Cole Parmer #R-45503-07)

  • Silicone tubing with large enough ID to slip over needle but small enough outer diameter (OD) to fit inside luer adapter.  We use 0.8 mm ID silicone tubing (Cole Parmer #R-06411-60)
  • Poly(dimethylsiloxane) (PDMS) (Sylgard 184, Dow Corning)
  • Tubing to attach to the connectors.  We use 0.51 mm ID tygon microbore tubing for 25 gauge needles (Cole Parmer #R-06418-02)
  • Dremel 300 (Dremel) or similar tool with cutoff wheel (Dremel #409)

How do I do it?


1. Insert the needle into the barbed end of the 1/16 in. barbed male luer adapter.
2. Thread about 15 mm of silicone tubing onto the needle and push the tubing to the base of the adapter using tweezers.  This keeps the needle centered in the adapter, and the silicone tubing bonds well to the PDMS.  The tubing should stick out of the adapter about 3mm, which accounts for extra dead space that exists in needle hubs and other female luer adapters.
3. Place the hubs of the needles you’ve made onto a dish standing upright.  Double-sided tape on the bottom of the dish will help keep the needles upright.
4. Fill the inside of the luer adapters with PDMS.  We find it helpful to use a syringe (with an 18 G needle) to inject PDMS into the adapters.  At this point it is recommended to de-gas the PDMS by placing it in a vacuum jar for several minutes.
5. Place the dish in an oven at 70ºC to cure for at least 2 hours.  Check after about an hour to make sure the luer hubs stayed filled with PDMS.  You may have to add some additional PDMS if some has leaked out the barbed end.
6. Remove the needle from the dish and clear away excess PDMS from the base of the needle and the outside of the adapter.
7. Push the adapter to the tip of the needle.
8. Cut away the needle luer hub.  A wire cutter can be used, but we prefer using a Dremel tool fitted with a cutting wheel.  It is less likely to compress the tubing closed.  Polishing the end of the needle with the cutting wheel is also recommended.
9. Insert the needle extending from the barbed end of the adapter into 0.51 mm ID Tygon tubing.

What else should I know?


“Quick connects” for the same or different ID tubing can be made by plugging the connector into the luer hub of a blunt needle that fits tightly inside the desired tubing.

We have also tried filling the luer hubs with PDMS and curing them prior to inserting needles or stainless steel tubing.  Because the needles are flexible, we find it difficult to keep the needles straight through the center of PDMS core.  This method also typically plugs the needle, so a new needle would be necessary to replace the coring needle.

Disclaimer: Certain commercial equipment, instruments or materials are identified in this report to specify adequately the experimental procedure. Such identification does not imply recommendation or endorsement by the National Institute of Standards and Technology, nor does it imply that the materials or equipment identified are necessarily the best available for the purpose.

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Connector-less manipulation of small liquid volumes in microchannels

Christopher Moraes, Yu Sun, and Craig A. Simmons
Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, Ontario, Canada

Why is this useful?


An often-touted advantage of microfluidic systems is the small volumes of reagents required.  However, the world-to-chip interconnects often require fluid volumes orders of magnitude greater than those used within the microfluidic channels themselves.  Moreover, commonly used interconnect schemes are either expensive; custom-manufactured or require substantial additional fabrication efforts; or are severely prone to failure, leaks and clogging.

This tip presents a simple, inexpensive and easily-accessible method to manipulate small volumes of fluid in standard microfabricated PDMS channels, without the use of a connector scheme.  Though it cannot be used to produce well-controlled or continuous long-term flow, we have found it ideal for applications such as device pre- and post-processing (e.g., chemical-based surface modification and immunostaining).  The technique is simple and robust, and has been used effectively both by experienced researchers and untrained, minimally supervised undergraduate students in a teaching lab.

What do I need?


  • Fully cured microfluidic PDMS device
  • Glass substrate
  • PDMS punch
  • 1 mL Pasteur pipette bulb (Sigma-Aldrich, product Z111589)
  • Pipettes and tips
  • Kimwipes

Figure 1

How do I do it?


1. Punch an access port into the PDMS device at the channel entry and exit points.  The size of the hole can be selected based on the reagent volume required by the device.  In this example, we used a 1/8″ diameter punch.

2. Bond the patterned PDMS layer to a glass slide, as per standard procedure for PDMS device fabrication.

3. Pipette a small quantity of reagent directly into the access port (Figure 1; blue dye used for this demonstration).  We have successfully used this technique with volumes as low as 4 mu.gifL.

4. Place the Pasteur pipette bulb (Figure 2) over the punched reservoir and gently hold it down so it forms a conformal seal around the reservoir (Figure 3).  Provided the area around the access port is fairly flat, maintaining a seal is typically not a problem.

Figure 2

Figure 3

5. Squeeze the bulb gently to apply positive pressure and cause the fluid to flow into the microchannels (Figure 4).

Figure 4

6. Channels can be cleared by first pipetting away excess fluid from the access port, and then using the Pasteur pipette bulb to force air through the channel, while wicking away the expelled liquid at the exit port with a Kimwipe.

The Pasteur pipette bulb can also be used to apply a negative pressure by squeezing it first, placing it over the channel access port, and gently releasing the bulb.  In Figure 5, we used this technique to drive flow in a standard microfluidic gradient generator system:  negative pressure is applied at the outlet channel port, drawing eight separated reagents through the mixing channels.

Figure 5

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