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A Parallel Microfluidic Channel Fixture Fabricated Using Laser Ablated Plastic Laminates for Electrochemical and Chemiluminescent Biodetection of DNA

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Date 2012 Jan 26
PMID 22276087
Citations 2
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Abstract

Herein is described the fabrication and use of a plastic multilayer 3-channel microfluidic fixture. Multilayer devices were produced by laser machining of plastic polymethylmethacrylate and polyethyleneterapthalate laminates by ablation. The fixture consisted of an array of nine individually addressable gold or gold/ITO working electrodes, and a resistive platinum heating element. Laser machining of both the fluidic pathways in the plastic laminates, and the stencil masks used for thermal evaporation to form electrode regions on the plastic laminates, enabled rapid and inexpensive implementation of design changes. Electrochemiluminescence reactions in the fixture were achieved and monitored through ITO electrodes. Electroaddressable aryl diazonium chemistry was employed to selectively pattern gold electrodes for electrochemical multianalyte DNA detection from double stranded DNA (dsDNA) samples. Electrochemical detection of dsDNA was achieved by melting of dsDNA molecules in solution with the integrated heater, allowing detection of DNA sequences specific to breast and colorectal cancers with a non-specific binding control. Following detection, the array surface could be renewed via high temperature (95 °C) stripping using the integrated heating element. This versatile and simple method for prototyping devices shows potential for further development of highly integrated, multi-functional bioanalytical devices.

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References
1.
Wang , Polsky , Tian , Chatrathi . Voltammetry on microfluidic chip platforms. Anal Chem. 2000; 72(21):5285-9. DOI: 10.1021/ac000484h. View

2.
Muck A, Svatos A . Chemical modification of polymeric microchip devices. Talanta. 2008; 74(3):333-41. DOI: 10.1016/j.talanta.2007.09.012. View

3.
McDonald J, Duffy D, ANDERSON J, Chiu D, Wu H, Schueller O . Fabrication of microfluidic systems in poly(dimethylsiloxane). Electrophoresis. 2000; 21(1):27-40. DOI: 10.1002/(SICI)1522-2683(20000101)21:1<27::AID-ELPS27>3.0.CO;2-C. View

4.
Wainright A, Nguyen U, Bjornson T, Boone T . Preconcentration and separation of double-stranded DNA fragments by electrophoresis in plastic microfluidic devices. Electrophoresis. 2003; 24(21):3784-92. DOI: 10.1002/elps.200305594. View

5.
Yager P, Edwards T, Fu E, Helton K, Nelson K, Tam M . Microfluidic diagnostic technologies for global public health. Nature. 2006; 442(7101):412-8. DOI: 10.1038/nature05064. View