Element-specific detection in capillary electrophoresis using X-ray fluorescence spectroscopy

被引:22
作者
Mann, SE [1 ]
Ringo, MC [1 ]
Shea-McCarthy, G [1 ]
Penner-Hahn, J [1 ]
Evans, CE [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
关键词
D O I
10.1021/ac9909608
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
X-ray fluorescence spectroscopy is demonstrated here as a novel, element-specific detector for capillary electrophoresis, Monochromatic 10 keV X-rays from a synchrotron light source are used to excite core electrons, causing emission of characteristic K alpha X-ray fluorescence (XRF) lines. Using this technique, XRF energies provide elemental identification, while XRF intensities can be used to quantitate the metal composition of each eluent. An X-ray transparent polymer coupling is used to create a window for the on-line, X-ray detection. This coupling contributes no measurable extra-column variance, and electrophoretic mobilities for the metal complexes used as model solutes are highly reproducible. The combination of XRF detection with capillary electrophoresis (CE-XRF) creates the first on-line detection system that is element-specific, nondestructive, and directly applicable to a broad range of applications including nonelectroactive species. CE-XRF is successfully demonstrated here for high binding-constant complexes of Fe(III), Co(II), Cu(II), and Zn(II), Within a single injection, electropherograms are obtained for each element of interest, with the element identity obtained directly from the emission energy. In contrast with ICPMS, this detection technique is directly on-line and does not require volatilization of the eluent, As a result, element-specific detection is not limited by the sample or the buffer volatility or atomization efficiency. Simultaneous XRF and UV absorbance detection can be used to provide an on-line determination of metal/chelate ratios. Although XRF detection limits are presently only in the 0.1 mM (0.5 ng) range, both collection geometry and incident intensity have yet to be optimized. Further optimization is expected to enhance this detection limit by another 2-3 orders of magnitude. As a result, the advent of XRF detection combined with the separating power of CE presents new possibilities for on-line, element-specific analysis.
引用
收藏
页码:1754 / 1758
页数:5
相关论文
共 31 条
[1]   Chemical profiles and monitoring dynamics at an individual nerve cell in Planorbis corneus with electrochemical detection [J].
Anderson, BB ;
Ewing, AG .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1999, 19 (1-2) :15-32
[2]   GRADIENT ELUTION FOR MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY [J].
BALCHUNAS, AT ;
SEPANIAK, MJ .
ANALYTICAL CHEMISTRY, 1988, 60 (07) :617-621
[3]   Capillary zone electrophoresis of proteins [J].
Dolník, V .
ELECTROPHORESIS, 1997, 18 (12-13) :2353-2361
[4]   PROTOCOL FOR RESOLVING PROTEIN MIXTURES IN CAPILLARY ZONE ELECTROPHORESIS [J].
GORDON, MJ ;
LEE, KJ ;
ARIAS, AA ;
ZARE, RN .
ANALYTICAL CHEMISTRY, 1991, 63 (01) :69-72
[5]  
Holland LA, 1998, ANAL COMMUN, V35, p1H
[6]   Structural and functional aspects of metal sites in biology [J].
Holm, RH ;
Kennepohl, P ;
Solomon, EI .
CHEMICAL REVIEWS, 1996, 96 (07) :2239-2314
[7]   Ultrahigh-voltage capillary zone electrophoresis [J].
Hutterer, KM ;
Jorgenson, JW .
ANALYTICAL CHEMISTRY, 1999, 71 (07) :1293-1297
[8]  
JENKINS R, 1998, XRAY FLUORESCENCE SP
[9]  
Kalinin BD, 1998, IND LAB+, V64, P85
[10]   ARSENIC SPECIATION IN SEAFOOD SAMPLES WITH EMPHASIS ON MINOR CONSTITUENTS - AN INVESTIGATION USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH DETECTION BY INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY [J].
LARSEN, EH ;
PRITZL, G ;
HANSEN, SH .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1993, 8 (08) :1075-1084