It's not often that someone can claim that going from a positive to a negative is a step forward, but that's the case for a team of scientists from the National Institute of Standards and Technology (NIST) and private industry. In a recent paper,* the group significantly extended the reach of their novel microfluidic system for analyzing the chemical components of complex samples. The new work shows how the system, meant to analyze real-world, crude mixtures such as dirt or whole blood, can work for negatively charged components as well as it has in the past for positively charged ones.
In previous work,** NIST researchers Elizabeth Strychalski and David Ross, in collaboration with Alyssa Henry of Applied Research Associates Inc. (Alexandria, Va.), demonstrated the use of a technique called GEMBE (for "gradient elution moving boundary electrophoresis") for analyzing complex samples. The NIST-developed system combines a simple microfluidic structure (two reservoirs connected by a microchannel), electrophoresis (which uses electricity to move sample components through a fluid) and pressure-driven flow.
Analyzing complex samples can be difficult because components in these samples (such as the fat globules in milk or proteins in blood) can "foul" or contaminate microfluidic channels. The traditional solution has been to remove contaminants with costly, time-consuming sample preparation prior to analysis.
GEMBE solves this problem by pumping fluid through the microchannel using a controlled pressure in the direction opposite to electrophoresis. This opposing pressure-driven flow acts as a "fluid gate" between the sample reservoir and the microchannel. Gradually reducing the pressure of the counterflow opens the "gate" a little bit at a time. A specific sample component is detected when the pressure flow becomes weak enoughi.e. the "gate" opens wide enoughthat the component's electrophoretic motion pushes it against the pressure-driven
|Contact: Michael E. Newman|
National Institute of Standards and Technology (NIST)