What is
Capillary Electrophoresis (CE)?
Background Of CE
Why Use CE?
What is Potential Gradient Detection?
Capillary electrophoresis(CE), similar to chromatography, is a technique for chemical analysis. It is generating tremendous interests in industrial labs due to its high sensitivity, high separation efficiency and rapid rate of analysis for many industrial applications. CE is able to accurately determine chemical compositions and detect trace impurities.
Even small deviations from process specification or minute amounts of contaminants can seriously affect product quality and yield in high technology manufacturing industries, such as semiconductor manufacturing and pharmaceutical production. CE enables composition or contaminant analysis to be accomplished fast, easily and accurately!
Capillary electrophoresis (CE) is a modern variant of electrophoresis in instrumentation. Electrophoresis is a separation technique based on the differential migration of electrically charged molecules or particles in a conductive liquid-based medium under the influence of an electric field. A distinctive feature of capillary electrophoresis is the use of small capillaries which have large ratios of area-to-volume. Efficient heat dissipation allows the use of high voltage which speeds the separation. All the capillary electrophoresis modes above can share the same instrumental setup, such as our portable CE system (Model CE-P1) or our conventional CE systems (CE-L1 with an detector).
Another format of capillary electrophoresis is performed on a microchip, namely microchip capillary electrophoresis. In addition, a lab-on-a-chip system can be used for accomplishing more complicated analytical tasks requiring highly integrated instrumentation.
Capillary electrophoresis, as a modern analytical technique, has been applied for inorganic ion analysis, environmental monitoring, water analysis, clinical analysis, food analysis, drug screening and biochemical analysis.
Potential gradient detection (PGD) is based on the changes in the electric field strength between zone boundaries during electrophoresis. The electric field strength is inversely proportional to the ionic mobility. Therefore, PGD originates from the differences in mobility between migrating zones, and is applicable to all charge-carrying compounds. It is similar to conductivity detection, but it does not need alternating or direct current. To measure the potential changes, two sensing electrodes are put longitudinally along the separation capillary. When sample components pass through the region between the two sensing electrodes, the potential from the two sensing electrodes will change and the analytes can be detected.