A modular microfluidic architecture for integrated biochemical analysis

被引:152
作者
Shaikh, KA
Ryu, KS
Goluch, ED
Nam, JM
Liu, JW
Thaxton, S
Chiesl, TN
Barron, AE
Lu, Y
Mirkin, CA
Liu, C [1 ]
机构
[1] Univ Illinois, Dept Elect & Comp Engn, Micro & Nanotechnol Lab, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60201 USA
[4] Northwestern Univ, Inst Nanotechnol, Evanston, IL 60201 USA
[5] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60201 USA
关键词
laboratory-on-a-chip; microfluidic breadboard; polydimethylsiloxane;
D O I
10.1073/pnas.0504082102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microfluidic laboratory-on-a-chip (LOC) systems based on a modular architecture are presented. The architecture is conceptualized on two levels: a single-chip level and a multiple-chip module (MCM) system level. At the individual chip level, a multilayer approach segregates components belonging to two fundamental categories: passive fluidic components (channels and reaction chambers) and active electromechanical control structures (sensors and actuators). This distinction is explicitly made to simplify the development process and minimize cost. Components belonging to these two categories are built separately on different physical layers and can communicate fluidically via cross-layer interconnects. The chip that hosts the electromechanical control structures is called the microfluidic breadboard (FBB). A single LOC module is constructed by attaching a chip comprised of a custom arrangement of fluid routing channels and reactors (passive chip) to the FBB. Many different LOC functions can be achieved by using different passive chips on an FBB with a standard resource configuration. Multiple modules can be interconnected to form a larger LOC system (MCM level). We demonstrated the utility of this architecture by developing systems for two separate biochemical applications: one for detection of protein markers of cancer and another for detection of metal ions. In the first case, free prostate-specific antigen was detected at 500 aM concentration by using a nanoparticle-based bio-bar-code protocol on a parallel MCM system. In the second case, we used a DNAzyme-based biosensor to identify the presence of Pb2+ (lead) at a sensitivity of 500 nM in < 1 nl of solution.
引用
收藏
页码:9745 / 9750
页数:6
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