Field-amplified sample stacking for the detection of chemical warfare agent degradation products in low-conductivity matrices by capillary electrophoresis-mass spectrometry

被引:35
作者
Lagarrigue, Manie [2 ]
Bossee, Anne [2 ]
Begos, Arlette [2 ]
Delaunay, Nathalie [1 ]
Varenne, Anne [1 ]
Gareil, Pierre [1 ]
Bellier, Bruno [2 ]
机构
[1] Ecole Natl Super Chim Paris, Lab Electrochim & Chim Analyt, F-75231 Paris, France
[2] Ctr Etud Bouchet, Dept Analyt Chim, F-91710 Vert Le Petit, France
关键词
alkylphosphonic acids; capillary electrophoresis-mass spectrometry (CE-MS); chemical warfare agent degradation products; environmental matrices; field-amplified sample stacking;
D O I
10.1016/j.chroma.2007.11.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Preconcentration of chemical warfare agent degradation products (alkylphosphonic acids and alkyl alkylphosphonic acids) in low-conductivity matrices (purified water, tap water and local river water) by field-amplified sample stacking (FASS) was developed for capillary electrophoresis (CE) coupled to ion trap mass spectrometry. FASS was performed by adding a mixture of HCOONH4 and NH4OH in appropriate concentrations to the sample. This allowed to control the conductivity and the pH of the sample in order to obtain FASS performances that are independent of analyte concentration. The influence of different parameters on FASS (sample to background electrolyte (BGE) conductivity ratio, injection volume and concentration of BGE) was studied to determine the optimal conditions and was rationalized by using the theoretical model developed by Burgi and Chien. A good correlation was obtained between the bulk electroosmotic velocity predicted by this model and the experimental value deduced from the migration time of the electroosmotic flow marker detected by mass spectrometry (MS). This newly developed method was successfully applied to the analysis of tap water and local river water fortified with the analytes and provided a 10-fold sensitivity enhancement in comparison to the signal obtained without preconcentration procedure. The quite satisfactory repeatability and linearity for peak areas obtained in the 0.5-5 mu g mL(-1) concentration range allow quantitative analysis to be implemented. Limits of detection of 0.25-0.5 mu g mL(-1) for the alkyl alkylphosphonic acids and of 0.35-5 mu g mL(-1) for the alkylphosphonic acids were reached in tap water and river water. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 247
页数:9
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