Chemistry and Physics Faculty Articles
Title
Interfacing Capillary-Based Separations to Mass Spectrometry Using Desorption Electrospray Ionization
Document Type
Article
Publication Date
2-14-2011
Publication Title
Analytical Chemistry
ISSN
0003-2700
Volume
83
Issue/No.
6
First Page
1955
Last Page
1959
Abstract
The powerful hybrid analysis method of capillary-based separations followed by mass spectrometric analysis gives substantial chemical identity and structural information. It is usually carried out using electrospray ionization. However, the salts and detergents used in the mobile phase for electrokinetic separations suppress ionization efficiencies and contaminate the inlet of the mass spectrometer. This report describes a new method that uses desorption electrospray ionization (DESI) to overcome these limitations. Effluent from capillary columns is deposited on a rotating Teflon disk that is covered with paper. As the surface rotates, the temporal separation of the eluting analytes (i.e., the electropherogram) is spatially encoded on the surface. Then, using DESI, surface-deposited analytes are preferentially ionized, reducing the effects of ion suppression and inlet contamination on signal. With the use of this novel approach, two capillary-based separations were performed: a mixture of the rhodamine dyes at milligram/milliliter levels in a 10 mM sodium borate solution was separated by capillary electrophoresis, and a mixture of three cardiac drugs at milligram/milliliter levels in a 12.5 mM sodium borate and 12.5 mM sodium dodecyl sulfate solution was separated by micellar electrokinetic chromatography. In both experiments, the negative effects of detergents and salts on the MS analyses were minimized.
Additional Comments
Air Force Office of Scientific Research grant #: FA 9550-10-1-0235; NSF grant #: PBEZP2-133126
NSUWorks Citation
Barbula, G. K., Safi, S., Chingin, K., Perry, R. H., & Zare, R. N. (2011). Interfacing Capillary-Based Separations to Mass Spectrometry Using Desorption Electrospray Ionization. Analytical Chemistry, 83, (6), 1955 - 1959. https://doi.org/10.1021/ac102648k. Retrieved from https://nsuworks.nova.edu/cnso_chemphys_facarticles/187
DOI
10.1021/ac102648k
Comments
©2011 American Chemical Society