Nanoliter-volume 1H NMR detection using periodic stopped-flow capillary electrophoresis

被引:105
作者
Olson, DL
Lacey, ME
Webb, AG
Sweedler, JV
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Beckman Inst, Urbana, IL 61801 USA
关键词
D O I
10.1021/ac990117+
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Recent advances in the analysis of nanoliter volumes using H-1 NMR microcoils have led to the application of microcoils as detectors for capillary electrophoresis (CE), Custom NMR probes consisting of 1-mm-long solenoidal microcoils are fabricated from 50-mu m diameter wire wrapped around capillaries to create nanoliter-volume detection cells. For geometries in which the capillary and static magnetic field are not parallel, the electrophoretic current induces a magnetic field gradient which degrades the spectroscopic information obtainable from CE/NMR. To reduce this effect and allow longer analyte observation times, the electrophoretic voltage is periodically interrupted so that 1-min high-resolution NMR spectra are obtained for every 15 s of applied voltage. The limits of detection (LODs; based on S/N = 3) for CE/NMR for arginine are 57 ng (330 pmol; 31 mM) and for triethylamine (TEA) are 9 ng (88 pmol; 11 mM). Field-amplified stacking is used for sample preconcentration. As one example, a 290-nL injection of a mixture of arginine and TEA both at 50 mM (15 nmol of each injected) is stacked severalfold for improved concentration LODs while achieving a separation efficiency greater than 50 000. Dissolving a sample in a mixture of 10% H2O/90% D2O allows H2O to serve as the nearly ideal neutral tracer and allows direct observation of the parabolic and flat flow profiles associated, with gravimetric and electrokinetic injection, respectively. The unique capabilities of CE and the rich spectral information provided by NMR spectroscopy combine to yield a valuable analytical tool, especially in the study of mass-limited samples.
引用
收藏
页码:3070 / 3076
页数:7
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