Microfluidic large-scale integration: The evolution of design rules for biological automation

被引:562
作者
Melin, Jessica [1 ]
Quake, Stephen R.
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Howard Hughes Med Inst, Stanford, CA 94305 USA
来源
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE | 2007年 / 36卷
关键词
soft lithography; biological automation; polydimethylsiloxane;
D O I
10.1146/annurev.biophys.36.040306.132646
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microfluidic large-scale integration (mLSI) refers to the development of microfluidic chips with thousands of integrated micromechanical valves and control components. This technology is utilized in many areas of biology and chemistry and is a candidate to replace today's conventional automation paradigm, which consists of fluid-handling robots. We review the basic development of mLSI and then discuss design principles of mLSI to assess the capabilities and limitations of the current state of the art and to facilitate the application of mLSI to areas of biology. Many design and practical issues, including economies of scale, parallelization strategies, multiplexing, and multistep biochemical processing, are discussed. Several microfluidic components used as building blocks to create effective, complex, and highly integrated microfluidic networks are also highlighted.
引用
收藏
页码:213 / 231
页数:19
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