A microfluidic device for on-chip agarose microbead generation with ultralow reagent consumption

被引:9
|
作者
Desbois, Linda [1 ]
Padirac, Adrien [1 ]
Kaneda, Shohei [1 ]
Genot, Anthony J. [1 ]
Rondelez, Yannick [1 ]
Hober, Didier [2 ,3 ]
Collard, Dominique [1 ]
Fujii, Teruo [1 ]
机构
[1] Univ Tokyo, LIMMS CNRS IIS, Inst Ind Sci, Meguro Ku, Tokyo 1538505, Japan
[2] Univ Lille 2, Fac Med, F-59120 Loos Lez Lille, France
[3] CHRU Lille, Lab Virol, EA 3610, F-59120 Loos Lez Lille, France
来源
BIOMICROFLUIDICS | 2012年 / 6卷 / 04期
关键词
biochemistry; biological techniques; bioMEMS; DNA; microfluidics; microreactors; molecular biophysics; POLYMERASE-CHAIN-REACTION; PARALLEL SINGLE-MOLECULE; DROPLET MICROFLUIDICS; HIGHLY PARALLEL; SCALE; EFFICIENT; PCR;
D O I
10.1063/1.4758460
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Water-in-oil microdroplets offer microreactors for compartmentalized biochemical reactions with high throughput. Recently, the combination with a sol-gel switch ability, using agarose-in-oil microdroplets, has increased the range of possible applications, allowing for example the capture of amplicons in the gel phase for the preservation of monoclonality during a PCR reaction. Here, we report a new method for generating such agarose-in-oil microdroplets on a microfluidic device, with minimized inlet dead volume, on-chip cooling, and in situ monitoring of biochemical reactions within the gelified microbeads. We used a flow-focusing microchannel network and successfully generated agarose microdroplets at room temperature using the "push-pull" method. This method consists in pushing the oil continuous phase only, while suction is applied to the device outlet. The agarose phase present at the inlet is thus aspirated in the device, and segmented in microdroplets. The cooling system consists of two copper wires embedded in the microfluidic device. The transition from agarose microdroplets to microbeads provides additional stability and facilitated manipulation. We demonstrate the potential of this method by performing on-chip a temperature-triggered DNA isothermal amplification in agarose microbeads. Our device thus provides a new way to generate microbeads with high throughput and no dead volume for biochemical applications. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4758460]
引用
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页数:10
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