Team:ETH Zurich/Process/Microfluidics

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|style="font-size:2em; height: 30px" class="process"|Development of Channel Design
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= Microfluidic Channel Design =
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'''For implementation of the SmoColi system, a channel is needed to establish a small molecule gradient (see [[Team:ETH_Zurich/Overview/Informationprocessing|Information processing]]). However, there were several different possible channel designs, and the final design evolved through an iterative series of design steps and design validations. The first designs were validated based on vast simulations, the final design furthermore by biological experiments in the lab (see [[Team:ETH_Zurich/Process/Validation|Systems Validation]]).'''
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|style="border-left: none;"|[[#Initial Channel Designs|Initial Channel Designs]]
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== Microfluidic channel with flow and recycling of the medium ==
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|[[#Final Channel Design|Final Channel Design]]
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We came up with two different possible '''microfluidic channel designs''', both involving immobilized cells and a flow of  medium containing inducer molecules  through the channel. By having a flow and degradation, we could obtain a '''gradient of the inducer molecule'''. Because of the flow, our cells would also be constantly supplied with nutrients from the medium.
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'''We figured out relatively early that we need some kind of channel to establish the acetaldehyde or xylene gradient required for SmoColi (see [[Team:ETH_Zurich/Overview/CircuitDesign|Circuit Design]]). However, there were several different possible channel designs, and the final design evolved through an iterative series of design steps and design validations. The first designs were validated based on vast simulations, the final design furthermore by biological experiments in the lab (see [[Team:ETH_Zurich/Process/Validation|Systems Validation]]).'''
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=== Microfluidic channel with flow and recycling of the medium ===
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* '''Variant 1: Microfluidic channel with agarose-immobilized cells in cubic pockets'''
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We came up with two different possible microfluidic channel designs, both involving immobilized cells and a flow of toxic molecule in medium through the channel. By having a flow and degradation, we could obtain nice gradient of the toxic molecule. Furthermore, with the flow our cells would be constantly supplied with nutrients from the medium.
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* '''Variant 1: Plate with cells-in-agarose-filled cubic "pixels" and a microfluidic channel above.'''
 
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This channel design consists of two parts: A PDMS plate with regular cubic "pixels" that is filled with cells in agarose by letting the cell-agarose solution flow over the pixels FROM THE TOP by gravity.  
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This channel design consists of two layers: The bottom one is a polydimethylsiloxane (PDMS) plate with regular cubic pockets. These pockets are filled with agarose-immobilized cells by letting the cell-agarose suspension flow over the pockets from the top by gravity. After washing the channel, cells would only be retained in the pockets. <br> <br>
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The top layer is the actual PDMS channel, which is several pixels wide and several pixels high. Although this setup is rather complex, it has the advantage of having immobilized cells and thus being more robust, i.e. we could vary flow speeds or even put aerosol in the channel without the cells being washed out. Additionally, cell density can be varied very easily in this design as the cells can be diluted before being immobilized in agarose.  
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The cell-agarose liquid is then cooled down and the solidified surplus cell-agarose gel scraped off.
 
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The second part is a larger PDMS channel, which is several pixels wide and several pixels high. It is then laid on top of the pixel structure and clamped tightly in order to create a seal. Although this setup is rather complex, it has the advantage of having immobilized cells and thus being more robust, i.e. we could vary flow speeds or even put aerosol in the channel without the cells being washed out. Additionally, cell density can be varied very easily in this design as the cells can be diluted before being immobilized in agarose.
 
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|valign="top"|[[File:flowchannel_pixel.png|500px|center|thumb|'''Figure 1: Experimental setup for SmoColi, Variant 1. ''' ]]
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|valign="top"|[[File:flowchannel_pixel.png|500px|center|thumb|'''Figure 1: Experimental setup for SmoColi channel, Variant 1. ''' ]]
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* '''Variant 2: Microfluidic channel with cells sitting in channel pockets. '''
 
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This channel design only consists of one part: A PDMS channel that is fixed onto a glass carrier. The PDMS channel contains pockets which "trap" the cells given a constant flow from the direction of the "open end" of the pockets. This channel design does not have the advantages of the above one, i.e. it is not as robust and cell density cannot be reliably varied. However, manufacturing it is a standard process and thus is easier.
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* '''Variant 2: Microfluidic channel with cells sitting in pockets inside the channel'''
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[[File:flowchannel_pockets.png|400px|center|thumb|'''Figure 2: Experimental setup for SmoColi, Variant 2. The flow is supplied from the right side of the illustration.''' ]]<br clear="all" />
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'''Problems with these design variants:''' A problem with both of these designs is that for the AHL-based RFP alarm to work, recycling of the flow back into the channel would be required. AHL-producing cells are only those "after" the GFP band, i.e. those at lower acetaldehyde concentration than the band concentration range. As long as the GFP band has not arrived until the end of the channel, we should make sure there is AHL everywhere in the channel, so that it inhibits RFP production in every cell. Modeling showed that AHL can not simply diffuse "backwards" against the flow, but by having a recycling all the cells would be supplied by AHL and thus the alarm won't be activated before time. 
 
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However, Since the tubing and pumps would have very high volumes compared to the channel volume, the AHL signal would be diluted to the point where no detection is possible anymore. Also, several pumps would be required to accomplish this, further complicating the process design and making it more error-prone.
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This channel design only consists of one part: A PDMS channel that is fixed onto a glass carrier. The PDMS channel contains pockets which "trap" the cells given a constant flow from the direction of the "open end" of the pockets. This channel design does not have the advantages of the above one, i.e. it is not as robust and cell density cannot be reliably varied. However, manufacturing it is a standard process and thus it is easier.
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=== Improved microfluidic channel without flow ===
 
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[[File:Setup_test.png|400px|right|thumb|'''Figure 3: Experimental setup for SmoColi, a tube with no flow, diffussion only''' ]]
 
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Modelling showed that diffusion and degradation of the toxic molecule is enough to create a nice concentration gradient in the channel. We checked that it will work not only in a microfluidics channel, but in a larger tube as well. In order to validate that experimentally and check if our cells can survive, we cloned them to express GFP upon IPTG induction and immobilized them in a small tube. We supplied them with IPTG from one side of the tube and after a while obtained a nice IPTG-inducible GFP gradient (see Figure 6 and 7). The experiment confirmed the modelling results. Our cells survived and we concluded that we don't need constant supply of nutrients.
 
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Without a flow there is no need for a moving liquid and thus no need for any of the complex designs above, as one can simply fill the whole channel with cell-agarose liquid. We can then wait until the cell-agarose liquid solidifies to a gel and then connect one side of the channel to a reservoir with the toxic molecule while sealing the other. Likewise we do not need recycling because AHL can diffuse through the whole channel and does not have to diffuse against a flow.
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[[File:flowchannel_pockets.png|400px|center|thumb|'''Figure 2: Experimental setup for SmoColi channel, Variant 2. The flow is supplied from the right side of the illustration.''' ]]<br clear="all" />
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'''Problems with these design variants:''' <br> <br>
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A problem with both of these designs is that for the AHL-based RFP alarm to work, recycling of the flow back into the channel would be required. AHL-producing cells are only those "after" the GFP band, i.e. those at lower acetaldehyde concentration than the band concentration range. As long as the GFP band has not arrived to the end of the channel, we should make sure that there is AHL everywhere in the channel, so that it inhibits RFP production in every cell. Modeling showed that AHL can not simply diffuse "backwards" against the flow, but by having a recycling all the cells would be supplied with AHL and thus the alarm won't be activated before time. 
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However, since the tubing and pumps would have very high volumes compared to the channel's volume, the AHL signal would be diluted to the point where no detection is possible anymore. Also, several pumps would be required to accomplish this, further complicating the process design and making it more error-prone. <br><br>
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== Improved microfluidic channel without flow ==
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[[File:Setup_test.png|500px|right|thumb|'''Figure 3: Experimental setup for SmoColi, a tube with no flow, diffusion only''' ]]
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Modeling showed that '''diffusion and degradation of the inducer is enough''' to create a concentration gradient in the channel. For proof of concept, we engineered E. coli strain JM101 to express GFP upon IPTG induction. The cells were immobilized in agarose and the suspension was added to the tube. One end of the tube was connected to a resevoir containing a IPTG solution. After incubation overnight, an IPTG-inducible GFP gradient could be observed. The experiment confirmed the modeling results. ''E. coli'' remained viable and we concluded that no flow was needed in our system setup. For more information about this [[Team:ETH Zurich/Process/Microfluidics/Proof|experimental setup and quantification of the results click here.]]<br><br>
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'''Problem with this design variant''': <br><br>No live imaging is possible, but only end point measurements, since the agarose with cells first has to be taken out of the tube and then analyzed under microscope.
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{{:Team:ETH Zurich/Templates/SectionEnd}}
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{{:Team:ETH Zurich/Templates/SectionStart}}
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== Further improvements: Microfluidic Channels with epoxy, molten parafilm or silicon ==
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Since live imaging in the tube was not possible, we tried to further improve our design to meet our experimental requirements. Thus we tried to pour our own channel with a reservoir included. Different substances as epoxy, molten parafilm or silicon were tested. As a mask we used plastic which we cut by hand.
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The channel was put on a object slide after solidification. Then the agarose-''E. coli'' suspension could be poured inside the channel.  
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Modeling the system thus had a profound effect on the process design, leading to an extensive reduction of complexity and error-proneness. Additionally, the AHL recycling idea would not have worked in the initial design, and was "saved" by the new channel design we developed by modeling our system.
 
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|valign="top"|[[File:ChannelPhoto.jpg|400px|center|thumb|'''Figure 4: Photo of the channel in action.''' The channel (the long thin tube at the right, 2 mm diameter, 7 cm length) is physically attached to a reservoir filled with the sample medium containing the toxic molecule, or in our test system with IPTG (the Eppendorf tube at the lower left). In the case of acetaldehyde, the whole setup would be packed in an impermeable plastic bag to significantly reduce the vaporization of acetaldehyde (not shown).]]
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|valign="top"|[[File:ETHZ_channel1.jpg|350px|center|thumb|'''Figure 4''': Tube (up) and plastic mask for channel construction (bottom) ]]
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|valign="top"|[[File:ChannelBlank.jpg|400px|center|thumb|'''After the experiment, the agarose gel containing the cells is removed from the tubing.''' Figure 5: The bald interior of the channel is placed on a petri dish (see picture) and analyzed under a fluorescence microscope.]]
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|valign="top"|[[File:ETHZ_channel2.jpg|410px|center|thumb|'''Figure 5''': Construction of microfluidic channels with silicon glue (left) and epoxy (right)]]
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Fluorescence pictures of the tube showed a clear gradient of the fluorescence signal over approximately 5 cm of the tube. After 5cm, the signal strength dropped under the background noise.
 
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[[File:ETHZ Gradient.png|800px|center|thumb|'''Figure 6: GFP gradient in tube:''' ''E. coli'' with IPTG-inducable GFP were incubated in a tube. GFP expression was assessed under the fluorescent microscope after overnight incubation, with a excitation wavelength of 480 nm and a emission wavelength of 510 nm. The 15 microscope photos were reassembled into one using [http://research.microsoft.com/en-us/um/redmond/groups/ivm/ICE/ the Microsoft Research Image Composite Editor].]]
 
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We quantified the fluorescence signal using a moving average of 80×80 pixel, which moved along the symmetry axis of the tube (see Figure 3), in red you can see the according reaction diffusion model.
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'''Problems with this design:'''<br><br>
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Figure 3: Quantification of the gradient in Figure 2: The light intensity of the IPTG-induced GFP signal was quantified by a 80×80 pixel moving average. The peak at around 1.2cm is due to an air bubble in the channel (see Figure 2).
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The glue turned out to be toxic for our cells.<br>
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We could also not use molten parafilm, since after putting it on the mask, the parafilm stuck to it and we could not remove the mask any more without destroying the channel (for molten parafilm a plastic mask is needed). <br>
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For silicon, we could get rid of this problem by covering the mask with oil. However, we had a problem with closing the channel tightly to prevent evaporation. Since this problem would occur with all of our designs, we decided to change it again.
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The fluorescence distribution of this experiment has a similar shape as the distributions predicted by the model (see modeling section). The difference in the experimental results compared to the simulations can be explained mainly due to the different diffusing molecules: the simulations were obtained for acetaldehyde, whereas the experiments were carried out with IPTG. We expect the different values of the diffusion as well as of the degradation constants of the two molecules to be the main reason for the differences.
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{{:Team:ETH Zurich/Templates/SectionEnd}}
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== Final Design: Microfluidics channel with PDMS ==
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'''Problem with this design variant''': No live imaging is possible, but only end point measurements, since the agarose with cells first has to be taken out of the tube and then analyzed under microscope.
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Finally, we decided to construct our channels out of something more frequently used: '''PDMS (polydimethylsiloxane)'''. To construct the channel, a technique called '''photolithography''' was used. Advantages of PDMS are that it is cheap, optically clear and permeable to several substances, including gases (air can quickly diffuse through) [[#Ref1|[1]]].  For the PDMS as well, as for the silicon channel we had problems with water evaporation. In order to solve this issue, in our final experimental setup we incubated the chips chontaining the channels in a petri dish full of water.<br>
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We constructed the PDMS channels ourselves, which was a very fun and interesting process. Our final design and the channel construction is explained in details [[Team:ETH_Zurich/Process/Validation|here]].
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{{:Team:ETH Zurich/Templates/SectionEnd}}
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{{:Team:ETH Zurich/Templates/SectionStart}}
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=== Further improving the channel material ===
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= References =
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With the tube live imaging is not possible, that´s why we develop our channel design further. To image the channel at the top and bottom of our channel a glas slide is needed. The channel itself we tried to build up by using a plastic mask and casting the boundaries with different materials. We tried Two-component glue, Silicon and molten parafilm. Two-component glue turned out to be toxic for our cells. Silicon and molten parafilm in contracts seen to be adequate for our channel.
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At the same time we tried something more frequently used, Polydimethylsiloxane (PDMS) for the channel.
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<span id="Ref1">[1] [http://www.elveflow.com/microfluidic/16-start-with-microfluidic http://www.elveflow.com/microfluidic/16-start-with-microfluidic]</span>
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=== Final System with PDMS channel===
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<gallery widths=240px heights=240px perrow=3 caption="Producing the channel">
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File:ETH MasK mikro.png
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File:Mikrofluidic negative.JPG
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File:Negative and PDMS.JPG
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Latest revision as of 00:42, 29 October 2011

Can you feel the smoke tonight?
 

Contents

Microfluidic Channel Design

For implementation of the SmoColi system, a channel is needed to establish a small molecule gradient (see Information processing). However, there were several different possible channel designs, and the final design evolved through an iterative series of design steps and design validations. The first designs were validated based on vast simulations, the final design furthermore by biological experiments in the lab (see Systems Validation).

Microfluidic channel with flow and recycling of the medium

We came up with two different possible microfluidic channel designs, both involving immobilized cells and a flow of medium containing inducer molecules through the channel. By having a flow and degradation, we could obtain a gradient of the inducer molecule. Because of the flow, our cells would also be constantly supplied with nutrients from the medium.


  • Variant 1: Microfluidic channel with agarose-immobilized cells in cubic pockets


This channel design consists of two layers: The bottom one is a polydimethylsiloxane (PDMS) plate with regular cubic pockets. These pockets are filled with agarose-immobilized cells by letting the cell-agarose suspension flow over the pockets from the top by gravity. After washing the channel, cells would only be retained in the pockets.

The top layer is the actual PDMS channel, which is several pixels wide and several pixels high. Although this setup is rather complex, it has the advantage of having immobilized cells and thus being more robust, i.e. we could vary flow speeds or even put aerosol in the channel without the cells being washed out. Additionally, cell density can be varied very easily in this design as the cells can be diluted before being immobilized in agarose.


Figure 1: Experimental setup for SmoColi channel, Variant 1.
Video 1: Evaluation of the model.


  • Variant 2: Microfluidic channel with cells sitting in pockets inside the channel


This channel design only consists of one part: A PDMS channel that is fixed onto a glass carrier. The PDMS channel contains pockets which "trap" the cells given a constant flow from the direction of the "open end" of the pockets. This channel design does not have the advantages of the above one, i.e. it is not as robust and cell density cannot be reliably varied. However, manufacturing it is a standard process and thus it is easier.


Figure 2: Experimental setup for SmoColi channel, Variant 2. The flow is supplied from the right side of the illustration.


Problems with these design variants:

A problem with both of these designs is that for the AHL-based RFP alarm to work, recycling of the flow back into the channel would be required. AHL-producing cells are only those "after" the GFP band, i.e. those at lower acetaldehyde concentration than the band concentration range. As long as the GFP band has not arrived to the end of the channel, we should make sure that there is AHL everywhere in the channel, so that it inhibits RFP production in every cell. Modeling showed that AHL can not simply diffuse "backwards" against the flow, but by having a recycling all the cells would be supplied with AHL and thus the alarm won't be activated before time.

However, since the tubing and pumps would have very high volumes compared to the channel's volume, the AHL signal would be diluted to the point where no detection is possible anymore. Also, several pumps would be required to accomplish this, further complicating the process design and making it more error-prone.


Improved microfluidic channel without flow

Figure 3: Experimental setup for SmoColi, a tube with no flow, diffusion only

Modeling showed that diffusion and degradation of the inducer is enough to create a concentration gradient in the channel. For proof of concept, we engineered E. coli strain JM101 to express GFP upon IPTG induction. The cells were immobilized in agarose and the suspension was added to the tube. One end of the tube was connected to a resevoir containing a IPTG solution. After incubation overnight, an IPTG-inducible GFP gradient could be observed. The experiment confirmed the modeling results. E. coli remained viable and we concluded that no flow was needed in our system setup. For more information about this experimental setup and quantification of the results click here.

Problem with this design variant:

No live imaging is possible, but only end point measurements, since the agarose with cells first has to be taken out of the tube and then analyzed under microscope.

Further improvements: Microfluidic Channels with epoxy, molten parafilm or silicon

Since live imaging in the tube was not possible, we tried to further improve our design to meet our experimental requirements. Thus we tried to pour our own channel with a reservoir included. Different substances as epoxy, molten parafilm or silicon were tested. As a mask we used plastic which we cut by hand. The channel was put on a object slide after solidification. Then the agarose-E. coli suspension could be poured inside the channel.


Figure 4: Tube (up) and plastic mask for channel construction (bottom)
Figure 5: Construction of microfluidic channels with silicon glue (left) and epoxy (right)


Problems with this design:

The glue turned out to be toxic for our cells.
We could also not use molten parafilm, since after putting it on the mask, the parafilm stuck to it and we could not remove the mask any more without destroying the channel (for molten parafilm a plastic mask is needed).
For silicon, we could get rid of this problem by covering the mask with oil. However, we had a problem with closing the channel tightly to prevent evaporation. Since this problem would occur with all of our designs, we decided to change it again.


Final Design: Microfluidics channel with PDMS

Finally, we decided to construct our channels out of something more frequently used: PDMS (polydimethylsiloxane). To construct the channel, a technique called photolithography was used. Advantages of PDMS are that it is cheap, optically clear and permeable to several substances, including gases (air can quickly diffuse through) [1]. For the PDMS as well, as for the silicon channel we had problems with water evaporation. In order to solve this issue, in our final experimental setup we incubated the chips chontaining the channels in a petri dish full of water.
We constructed the PDMS channels ourselves, which was a very fun and interesting process. Our final design and the channel construction is explained in details here.

References

[1] [http://www.elveflow.com/microfluidic/16-start-with-microfluidic http://www.elveflow.com/microfluidic/16-start-with-microfluidic]


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