Abstract
Microfluidics and integrated microsystems are the current focus of unusually intense interest and activity on the part of academia, industry, and governmental agencies, an assertion substantiated by the solid attendance at the 2003 International Conference on Micro Total Analysis Systems (µTAS) [45] and by the recent publication of various books on this topic [46], both at a time when the economy in general, and the technology sector in particular, are at relative low points. Significant advances have been realized since the concept of µTAS was developed more than a decade ago as a means to enhance versatility and functionality relative to discrete chemical sensor devices [41]. Functional examples of the µTAS concept include on-chip PCR (polymerase chain reaction) [28, 44, 72], DNA analysis and sequencing [14, 58, 76], immunoassays [10, 19, 57], protein separations [23, 48, 64], and intra- and inter-cellular analysis [29, 53, 63]. Advantages of these µ-TAS over bench-top instruments include low reagent consumption, small sample volumes, high separation efficiencies, short reaction times, ease of automation, and potential for massproduction with low cost [41].
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Fan, Z.H., Ricco, A.J. (2006). Plastic Microfluidic Devices for DNA and Protein Analyses. In: Ferrari, M., Ozkan, M., Heller, M.J. (eds) BioMEMS and Biomedical Nanotechnology. Springer, Boston, MA. https://doi.org/10.1007/978-0-387-25843-0_9
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DOI: https://doi.org/10.1007/978-0-387-25843-0_9
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