Team:TU Eindhoven/Modeling/Cell Encapsulation Modeling

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                   <h2>Cell Encapsulation Modeling</h2>
                   <h2>Cell Encapsulation Modeling</h2>
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                   <p>The modeling group focused on the microfluidics. With microfluidics the cells are separated into a single droplet. This process however is not very accurate. Sometimes the droplets do not contain the desired number of cells. This can be modelled using a Poisson distribution. In this model you can define an average number of cells per droplet, lambda. Lambda was varied to choose a suitable average number of cells per droplet for our microfluidic device.</p>
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                   <p>The modeling group focused on the microfluidics. With microfluidics the cells are separated into single droplets. However, this process however is not very accurate. Sometimes the droplets do not contain the desired number of cells. This can be modeled using a Poisson distribution. In this model one can define an average number of cells per droplet, lambda. Lambda was varied to choose a suitable average number of cells per droplet for our microfluidic device.</p>
<img id='Fig1' src="https://static.igem.org/mediawiki/2014/5/50/TU_Eindhoven_Poisson_distribution.jpg" class="image_wrapper image_fr" width="1085">
<img id='Fig1' src="https://static.igem.org/mediawiki/2014/5/50/TU_Eindhoven_Poisson_distribution.jpg" class="image_wrapper image_fr" width="1085">
<p style="font-size:18px;color:#CCCCCC;">Figure 1. Poisson distribution for multiple lambdas.</p>
<p style="font-size:18px;color:#CCCCCC;">Figure 1. Poisson distribution for multiple lambdas.</p>
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<p>This allows for the determination of the ratios between one cell/zero cells and one cell/ two or more cells. These both have to be as high as possible for a specific lambda.</p>
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<p>This allows for the determination of the ratios between one cell/zero cells and one cell/ two or more cells. Both of these have to be as high as possible for a specific lambda.</p>
<img id='Fig2' src="https://static.igem.org/mediawiki/2014/0/09/TU_Eindhoven_Modeling2.jpg" class="image_wrapper image_fr" width="1085">
<img id='Fig2' src="https://static.igem.org/mediawiki/2014/0/09/TU_Eindhoven_Modeling2.jpg" class="image_wrapper image_fr" width="1085">

Revision as of 23:55, 17 October 2014

iGEM Team TU Eindhoven 2014

iGEM Team TU Eindhoven 2014

Cell Encapsulation Modeling

The modeling group focused on the microfluidics. With microfluidics the cells are separated into single droplets. However, this process however is not very accurate. Sometimes the droplets do not contain the desired number of cells. This can be modeled using a Poisson distribution. In this model one can define an average number of cells per droplet, lambda. Lambda was varied to choose a suitable average number of cells per droplet for our microfluidic device.

Figure 1. Poisson distribution for multiple lambdas.

This allows for the determination of the ratios between one cell/zero cells and one cell/ two or more cells. Both of these have to be as high as possible for a specific lambda.

Figure 2. Ratio between one cell/ zero cells or more cells

Based on these results a lambda of 0.3 was chosen for the microfluidic device. The Poisson distribution for different number of cells becomes then as follows.

Figure 3. Modeled Poisson distribution for a specific lambda of 0.3 together with vs. the experimental Poisson distribution based on a lambda of 0.3.

Click here to download the model

Bibliography

Mazutis, Linas, John Gilbert, W Lloyd Ung, David A Weitz, Andrew D Griffiths and John A Heyman. Single-cell analysis and sorting using droplet-based microfluidics. Nature protocols 8.5 (2013): 870-891.

iGEM Team TU Eindhoven 2014