Focal volume confinement by submicrometer-sized fluidic channels.

Anal Chem

School of Applied & Engineering Physics, Cornell University, Ithaca, New York 14853, USA.

Published: March 2004

AI Article Synopsis

  • Microfluidic channels under 1 microm in size were created in fused silica, allowing for sensitive detection of single molecules and improved fluorescence correlation spectroscopy.
  • These channels provide observation volumes that are around 100 times smaller than traditional methods, enabling better detection even at higher concentrations.
  • The design enables fast analyte flow using electrokinetic forces, leading to quicker detection times and enhanced statistical accuracy in analyzing single molecules, with potential applications in drug screening and genomic studies.

Article Abstract

Microfluidic channels with two lateral dimensions smaller than 1 microm were fabricated in fused silica for high-sensitivity single-molecule detection and fluorescence correlation spectroscopy. The effective observation volumes created by these channels are approximately 100 times smaller than observation volumes using conventional confocal optics and thus enable single-fluorophore detection at higher concentrations. Increased signal-to-noise ratios are also attained because the molecules are restricted to diffuse through the central regions of the excitation volume. Depending on the channel geometries, the effective dimensionality of diffusion is reduced, which is taken into account by simple solutions to diffusion models with boundaries. Driven by electrokinetic forces, analytes could be flowed rapidly through the observation volume, drastically increasing the rate of detection events and reducing data acquisition times. The statistical accuracy of single-molecule characterization is improved because all molecules are counted and contribute to the analysis. Velocities as high as 0.1 m/s were reached, corresponding to average molecular residence times in the observation volume as short as 10 micros. Applications of these nanofabricated devices for high-throughput, single-molecule detection in drug screening and genomic analysis are discussed.

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http://dx.doi.org/10.1021/ac035088oDOI Listing

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