28 April 2010 Parallel microfluidic arrays for SPRi detection
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Abstract
Surface Plasmon Resonance imaging (SPRi) is a label-free technique for the quantitation of binding affinities and concentrations for a wide variety of target molecules. Although SPRi is capable of determining binding constants for multiple ligands in parallel, current commercial instruments are limited to a single analyte stream and a limited number of ligand spots. Measurement of target concentration also requires the serial introduction of different target concentrations; such repeated experiments are conducted manually and are therefore time-intensive. Likewise, the equilibrium determination of concentration for known binding affinity requires long times due to diffusion-limited kinetics to a surface-immobilized ligand. We have developed an integrated microfluidic array using soft lithography techniques for SPRi-based detection and determination of binding affinities for DNA aptamers against human alphathrombin. The device consists of 264 element-addressable chambers of 700 pL each isolated by microvalves. The device also contains a dilution network for simultaneous interrogation of up to six different target concentrations, further speeding detection times. The element-addressable design of the array allows interrogation of multiple ligands against multiple targets, and analytes from individual chambers may be collected for downstream analysis.
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Eric Ouellet, Eric Ouellet, Christopher Lausted, Christopher Lausted, Tao Lin, Tao Lin, Cheng-Wei Yang, Cheng-Wei Yang, Leroy Hood, Leroy Hood, Eric T. Lagally, Eric T. Lagally, } "Parallel microfluidic arrays for SPRi detection", Proc. SPIE 7682, Photonic Microdevices/Microstructures for Sensing II, 76820F (28 April 2010); doi: 10.1117/12.850522; https://doi.org/10.1117/12.850522
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