4.7 Article

Novel technologies for the formation of 2-D and 3-D droplet interface bilayer networks

期刊

LAB ON A CHIP
卷 12, 期 18, 页码 3514-3520

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2lc40287d

关键词

-

资金

  1. EPSRC [EP/G00465X/1, EP/H024425/1]
  2. BBSRC [BB/F013167/1]
  3. EPSRC Centre for Doctoral Training Studentship from the Institute of Chemical Biology (Imperial College London)
  4. BBSRC [BB/F013167/1] Funding Source: UKRI
  5. EPSRC [EP/G00465X/1, EP/H024425/1, EP/I501053/1] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BB/F013167/1] Funding Source: researchfish
  7. Engineering and Physical Sciences Research Council [EP/H024425/1, EP/I501053/1, 1101745, EP/G00465X/1] Funding Source: researchfish

向作者/读者索取更多资源

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 the 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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据