What molecule or particle passes the finishline first? A good way to split a fluid sample into its separate parts is: organize a contest in a micro-channel. The largest parts will pass the optical detector first, the smaller ones follow at short distance. This principle of ‘hydrodynamic chromatography’ is now also possible on a chip. ‘On-chip’ separation is faster, needs tiny samples and uses minimum of harmful solvents. Marko Blom developed this separation chip within the MESA+ research institute of the University of Twente. He presents his PhD-work on December 13, 2002.
The separation channel Blom has developed is not deeper than one micron, it is one millimeter in width and some six to eight centimeters long. It has been fabricated in silicon or silicate glass. Thanks to this compact geometry, the separation is fast: bigger molecules move faster, smaller ones follow. A light-sensitive cell detects the fastest ones first. Colour characteristics provide additional information about the particle or molecule: therefore at the start of the ‘race’, fluorescent markers can be added to the fluid, for example.
Hydrodynamic chromatography (HDC) is a well-known separation technique for particles and large molecules, but the resolution of current methods is far from optimal. HDC is usually applied in a fluid column, filled with non-porous particles that create, with the tiny spaces inbetween, the same effect as a narrow channel. On-chip separation results in a better resolution because the geometry is better defined than the pores between the particles in a conventional column, that are divided in a rather arbitrary way. Within just a few minutes Blom can, for example, fully separate little polystyrene balls. The new chip is particularly interesting for analysis of large molecules like polymers. For biomolecules, it works as well: for example analysis of DNA-components.
Wiebe van der Veen | alfa
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