Microfluidic very large scale integration (mVLSI) with integrated micromechanical valves

被引:172
作者
Araci, Ismail Emre [1 ]
Quake, Stephen R.
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
关键词
DEVICES; POLY(DIMETHYLSILOXANE); INTERFACE;
D O I
10.1039/c2lc40258k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microfluidic chips with a high density of control elements are required to improve device performance parameters, such as throughput, sensitivity and dynamic range. In order to realize robust and accessible high-density microfluidic chips, we have fabricated a monolithic PDMS valve architecture with three layers, replacing the commonly used two-layer design. The design is realized through multi-layer soft lithography techniques, making it low cost and easy to fabricate. By carefully determining the process conditions of PDMS, we have demonstrated that 8 x 8 and 6 x 6 mu m(2) valve sizes can be operated at around 180 and 280 kPa differential pressure, respectively. We have shown that these valves can be fabricated at densities approaching 1 million valves per cm(2), substantially exceeding the current state of the art of microfluidic large-scale integration (mLSI) (thousands of valves per cm(2)). Because the density increase is greater than two orders of magnitude, we describe this technology as microfluidic very large scale integration (mVLSI), analogous to its electronic counterpart. We have captured and tracked fluorescent beads, and changed the electrical resistance of a fluidic channel by using these miniaturized valves in two different experiments, demonstrating that the valves are leakproof. We have also demonstrated that these valves can be addressed through multiplexing.
引用
收藏
页码:2803 / 2806
页数:4
相关论文
共 23 条
[1]  
Anderson MJ, 2005, BIOPHYS J, V88, p55A
[2]   Electromechanical properties of pressure-actuated poly(dimethylsiloxane) microfluidic push-down valves [J].
Chen, Hao ;
Gu, Wei ;
Cellar, Nick ;
Kennedy, Robert ;
Takayama, Shuichi ;
Meiners, Jens-Christian .
ANALYTICAL CHEMISTRY, 2008, 80 (15) :6110-6113
[3]   Control and detection of chemical reactions in microfluidic systems [J].
deMello, Andrew J. .
NATURE, 2006, 442 (7101) :394-402
[4]   Whole-genome molecular haplotyping of single cells [J].
Fan, H. Christina ;
Wang, Jianbin ;
Potanina, Anastasia ;
Quake, Stephen R. .
NATURE BIOTECHNOLOGY, 2011, 29 (01) :51-+
[5]   An integrated microfluidic processor for single nucleotide polymorphism-based DNA computing [J].
Grover, WH ;
Mathies, RA .
LAB ON A CHIP, 2005, 5 (10) :1033-1040
[6]  
Heyries KA, 2011, NAT METHODS, V8, P649, DOI [10.1038/NMETH.1640, 10.1038/nmeth.1640]
[7]  
Jensen C., 2010, JALA, V15, P455
[8]   Protein Crystallization Using Microfluidic Technologies Based on Valves, Droplets and SlipChip [J].
Li, Liang ;
Ismagilov, Rustem F. .
ANNUAL REVIEW OF BIOPHYSICS, VOL 39, 2010, 39 :139-158
[9]   Solving the "world-to-chip" interface problem with a microfluidic matrix [J].
Liu, J ;
Hansen, C ;
Quake, SR .
ANALYTICAL CHEMISTRY, 2003, 75 (18) :4718-4723
[10]   Self-contained, fully integrated biochip for sample preparation, polymerase chain reaction amplification, and DNA microarray detection [J].
Liu, RH ;
Yang, JN ;
Lenigk, R ;
Bonanno, J ;
Grodzinski, P .
ANALYTICAL CHEMISTRY, 2004, 76 (07) :1824-1831