Novel technologies for the formation of 2-D and 3-D droplet interface bilayer networks
Novel technologies for the formation of 2-D and 3-D droplet interface bilayer networks
Droplet Interface Bilayer (DIB) networks have vast potential in the field of membrane biophysics, synthetic biology, and functional bio-electronics. However a technological bottleneck exists in network fabrication: existing methods are limited in terms of their automation, throughput, versatility, and ability to form well defined 3-D networks. We have developed a series of novel and low-cost methodologies which address these limitations. The first involves building DIB networks around the contours of a microfluidic chip. The second uses flow rate and droplet size control to influence droplet packing geometries within a microfluidic chamber. The latter method enables controlled formation of various 3-D network arrays consisting of thousands of interconnected symmetric and asymmetric lipid bilayers for the first time. Both approaches allow individual droplet position and composition to be controlled, paving the way for complex on-chip functional network synthesis.
Elani, Yuval
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Niu, Xize
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deMello, Andrew
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Ces, Oscar
3dc0f432-42f3-4308-acc9-e17271c74068
17 July 2012
Elani, Yuval
daf4c0fd-cd14-4cd3-928c-e18ffafc6eae
Niu, Xize
f3d964fb-23b4-45db-92fe-02426e4e76fa
deMello, Andrew
2b4a1c10-da98-4289-9dec-2db42e4a4b03
Ces, Oscar
3dc0f432-42f3-4308-acc9-e17271c74068
Elani, Yuval, Niu, Xize, deMello, Andrew and Ces, Oscar
(2012)
Novel technologies for the formation of 2-D and 3-D droplet interface bilayer networks.
Lab on a Chip.
(doi:10.1039/C2LC40287D).
Abstract
Droplet Interface Bilayer (DIB) networks have vast potential in the field of membrane biophysics, synthetic biology, and functional bio-electronics. However a technological bottleneck exists in network fabrication: existing methods are limited in terms of their automation, throughput, versatility, and ability to form well defined 3-D networks. We have developed a series of novel and low-cost methodologies which address these limitations. The first involves building DIB networks around the contours of a microfluidic chip. The second uses flow rate and droplet size control to influence droplet packing geometries within a microfluidic chamber. The latter method enables controlled formation of various 3-D network arrays consisting of thousands of interconnected symmetric and asymmetric lipid bilayers for the first time. Both approaches allow individual droplet position and composition to be controlled, paving the way for complex on-chip functional network synthesis.
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Published date: 17 July 2012
Organisations:
Mechatronics
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Local EPrints ID: 341334
URI: http://eprints.soton.ac.uk/id/eprint/341334
ISSN: 1473-0197
PURE UUID: 9f243b5b-5fed-4461-a6d7-d1e9fc73d2c2
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Date deposited: 23 Jul 2012 11:15
Last modified: 14 Mar 2024 11:38
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Author:
Yuval Elani
Author:
Andrew deMello
Author:
Oscar Ces
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