On-chip magnetic separation and encapsulation of cells in droplets.
On-chip magnetic separation and encapsulation of cells in droplets.
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DOI:
10.1039/c2lc41201b
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发表时间:
2013-03-21
期刊:
影响因子:
6.1
通讯作者:
Sooryakumar R
中科院分区:
文献类型:
--
作者:
Chen A;Byvank T;Chang WJ;Bharde A;Vieira G;Miller BL;Chalmers JJ;Bashir R;Sooryakumar R
The demand for high-throughput single cell assays is gaining importance because of the heterogeneity of many cell suspensions, even after significant initial sorting. These suspensions may display cell-to-cell variability at the gene expression level that could impact single cell functional genomics, cancer, stem-cell research and drug screening. The on-chip monitoring of individual cells in an isolated environment would prevent cross-contamination, provide high recovery yield, and enable study of biological traits at a single cell level. These advantages of on-chip biological experiments is a significant improvement for myriad of cell analyses over conventional methods, which require bulk samples providing only averaged information on cell metabolism. We report on a device that integrates mobile magnetic trap array with microfluidic technology to provide, combined functionality of separation of immunomagnetically labeled cells or magnetic beads and their encapsulation with reagents into pico-liter droplets. This scheme of simultaneous reagent delivery and compartmentalization of the cells immediately after sorting, all performed seamlessly within the same chip, offers unique advantages such as the ability to capture cell traits as originated from its native environment, reduced chance of contamination, minimal use and freshness of the reagent solution that reacts only with separated objects, and tunable encapsulation characteristics independent of the input flow. In addition to the demonstrated preliminary cell viability assay, the device can potentially be integrated with other up- or downstream on-chip modules to become a powerful single-cell analysis tool.
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影响因子:
46.9
作者:
通讯作者:
--
DOI:
10.1073/pnas.92.3.860
发表时间:
1995-01-31
影响因子:
11.1
作者:
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通讯作者:
GASCOYNE, PRC
影响因子:
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通讯作者:
Sturm, JC
影响因子:
4
作者:
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通讯作者:
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影响因子:
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作者:
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通讯作者:
Frazier, A. Bruno