Selective trace enrichment by immunoaffinity capillary electrochromatography on-line with capillary zone electrophoresis - laser-induced fluorescence

被引:0
|
作者
Thomas, DH
Rakestraw, DJ
Schoeniger, JS
Lopez-Avila, V
Van Emon, J
机构
[1] Sandia Natl Labs, Livermore, CA 94551 USA
[2] Midwest Res Inst, Calif Operat, Mt View, CA USA
[3] US EPA, Natl Exposure Res Lab, Human Exposure Res Branch, Las Vegas, NV 89193 USA
关键词
immunoaffinity; capillary; electrochromatography; miniaturization;
D O I
10.1002/(SICI)1522-2683(19990101)20:1<57::AID-ELPS57>3.0.CO;2-J
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Limited by the lack of a sensitive, universal detector, many capillary-based liquid-phase separation techniques might benefit from techniques that overcome modest concentration sensitivity by preconcentrating large injection volumes. The work presented employs selective solid-phase extraction by immunoaffinity capillary electrochromatography (IACEC) to enhance detection limits. A model analyte, fluorescein isothiocyanate (FITC) biotin, is electrokinetically applied to a capillary column packed with an immobilized anti-biotin-IgG support. After selective extraction by the immunoaffinity capillary, the bound analyte is eluted, migrates by capillary zone electrophoresis (CZE), and is detected by laser-induced fluorescence. The column is regenerated and reused many times. We evaluate the performance of IACEC for selective trace enrichment of analytes prior to CZE. The calibration curve for FITC-biotin bound versus application time is linear from 10 to 300 seconds. Recovery of FITC-biotin spiked into a diluted urinary metabolites solution was 89.4% Versus spiked buffer, with a precision of 1.8% relative standard deviation (RSD).
引用
收藏
页码:57 / 66
页数:10
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