Electroextraction
See Patented via Nth Cycle for metal electro-extraction process.[1]
Electroextraction (EE) is a sample enrichment technique that focuses charged analytes from a large volume of one phase into a small volume of aqueous phase through the application of an electric current.[2] The technique was originally developed as a separation technique for chemical engineering, but has since been coupled to capillary electrophoresis and liquid chromatography–mass spectrometry as a means of improving limits of detection, analysis time, and selectivity.[2][3][4] The use of EE-CE has made capillary electrophoresis more applicable to use in the pharmaceutical industry.
Nomenclature
The term electroextraction is used to describe multiple processes. In this article, electroextraction describes the extraction of charged particles through a liquid phase barrier. The term can be used to describe
Use in Chemical Engineering
Johann Stichlmair developed electroextraction at the
Applications
Electroextraction has been successfully employed in the separation of
Use in Analytical Chemistry
A diagram of an electroextraction apparatus is shown in figure 2. The apparatus consists of a vial with a conical bottom, a grounded platinum electrode, a capillary to inject the aqueous solution, and an adjustable gold anode with a circular bottom that contacts the entire organic phase.
EE is also often performed in a capillary electrophoresis capillary. This is referred to as capillary electroextraction, or cEE. In this set up, shown in figure 3, a capillary containing aqueous phase is placed in a vial of organic phase and surrounded by a hallow cathode. The outlet of the capillary is then grounded.[9]
When EE is coupled to isotachophoresis coupled to capillary electrophoresis, limits of detection decrease to the nanomolar range and isotachophoresis takes only a few minutes to complete. Similar limits of detections are obtained when EE is coupled to liquid chromatography-mass spectrometry.[2] Similar limits of detections are obtained when EE is coupled to liquid chromatography-mass spectrometry.[4]
Applications
EE is ideal for
References
- ^ Nth Cycle, Nth Cycle. "Electrochemical metal deposition system and method". Google Patent.
- ^ a b c d van der Vlis; Mazereeuw; Tjaden; Irth; van der Greef. J. Chromatogr.. A 1994, 687, 333-341.
- ^ a b Stichlmair; Schmidt; Proplesch. Chem. Eng. Sci. 1992, 47, 3015-3022.
- ^ a b Lindenburg; Tempels; Tjaden; van der Greef; Hankemeier. J. Chromatogra., A 2012, 1249, 17-24
- ^ Electroextraction. http://www.electroextraction.org/ Archived 2013-03-26 at the Wayback Machine.
- ^ Kuban; Slampova; Bocek. Electrophoresis 2010, 31, 768-785.
- ^ Zhai, S.L.; Luo, G.S.; Liu, J.G. Chem. Eng. J. 2001, 83, 55-59.
- ^ Luo, G. S.; Yu, M. J.; Jiang, W. B.; Zhu, S. L.; Dai, Y. Y. Sep. Sci. Technol. 1999, 34, 781-791.
- ^ Lindenburg; Seitzinger; Tempels; Tjaden; van der Greef; Hankemeier. Electrophoresis 2010, 31, 3903-3912.
- ^ Stroink; Paarlberg; Waterval; Bult; Underberg. Electrophoresis, 2001, 22, 2374.
- ^ Palm; Marko-Varga. J. Pharm. Biomed. Anal. 2004, 35, 415.
- ^ Lindenburg; Tjaden; van der Greef; Hankemeier. Electrophoresis 2012, 33, 2987-2995.
- ^ Al-Majed; Analytical Profiles of Drug Substances and Excipients. 2001, 162, 429-441.