Team:BIOTEC Dresden/Results Vesicles

From 2009.igem.org

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The vesicles have been observed in the monitoring section of the microfluidic chamber. Figure 1 shows a typical vesicle moving through a channel.
The vesicles have been observed in the monitoring section of the microfluidic chamber. Figure 1 shows a typical vesicle moving through a channel.
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A microfluidic chamber that created an intersection between aqueous and oil phases produced vesicles that were uniform in size and stable for up to 5 hours. The vesicles are stabilized by a surfactant, Span 80.
A microfluidic chamber that created an intersection between aqueous and oil phases produced vesicles that were uniform in size and stable for up to 5 hours. The vesicles are stabilized by a surfactant, Span 80.
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Revision as of 02:44, 22 October 2009

Vesicle formation in Microfluidic Chamber

The video shows the formation of vesicles in a V-chamber. The surfactant Span 80 at a concentration (V/V) of 1% was dissolved in the oil phase. The flow rates used were different for every chamber used and are hence not transferable to other systems. Vesicle size varied with applied flow rates: increased flow rates of the aqueous phase yielded in larger vesicles. Above a critical flow rate the aqueous phase would displace the oil phase.

Vesicle formation in V-chamber. Surfactant: 1% Span 80

The vesicles have been observed in the monitoring section of the microfluidic chamber. Figure 1 shows a typical vesicle moving through a channel.

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A microfluidic chamber that created an intersection between aqueous and oil phases produced vesicles that were uniform in size and stable for up to 5 hours. The vesicles are stabilized by a surfactant, Span 80.


Vesicles are led into a grid by funnel shaped structures in the flow chamber (top).

Here are more results:

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Retrieved from "http://2009.igem.org/Team:BIOTEC_Dresden/Results_Vesicles"