Separation of proteins on surface-modified poly(dimethylsiloxane) microfluidic devices

Electrophoresis. 2004 Sep;25(17):3024-31. doi: 10.1002/elps.200405986.

Abstract

Separation and detection of proteins have been realized on nonionic surfactant-modified poly(dimethylsiloxane) (PDMS) microfabricated devices with end-column amperometric detection. The hydrophobic PDMS channels are turned into hydrophilic ones after being modified with Brij35 and facilitate the separation of proteins. The coating can remarkably reduce the adsorption of large protein molecules and is stable in the range of pH 6-12. The detection of proteins in such channels needs less rinsing time and thus efficiency is raised. Even large molecules of proteins can also be detected with better reproducibility and enhanced plate numbers. The relative standard deviation (RSD) of the migration time for glucose oxidase (GOD) is 2.2% (n = 19). Separation of GOD and myoglobin has been developed in modified channels. Predominant operational variables, such as the coating conditions, the concentration of surfactant and buffer, are studied in detail.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dimethylpolysiloxanes*
  • Electrochemistry / methods
  • Electrophoresis / methods
  • Indicators and Reagents
  • Microchemistry
  • Microchip Analytical Procedures / methods
  • Microfluidic Analytical Techniques / methods
  • Myoglobin / isolation & purification*
  • Reproducibility of Results
  • Surface Properties

Substances

  • Dimethylpolysiloxanes
  • Indicators and Reagents
  • Myoglobin