Determination of sulfonamide residues in water samples by in-line solid-phase extraction-capillary electrophoresis

被引:70
作者
Lara, Francisco J. [1 ]
Garcia-Campana, Ana M. [1 ]
Neusuess, Christian [2 ]
Ales-Barrero, Fermin [1 ]
机构
[1] Univ Granada, Dept Analyt Chem, Fac Sci, E-18071 Granada, Spain
[2] Aalen Univ, Fac Chem, D-73430 Aalen, Germany
关键词
Sulfonamides; Water samples; Capillary electrophoresis; In-line solid-phase extraction; Analyte concentrator; ELECTROSPRAY-MASS-SPECTROMETRY; ION-EXCHANGE PRECONCENTRATION; SWINE WASTE-WATER; OPEN-TUBULAR CAPILLARIES; LIQUID-CHROMATOGRAPHY; SURFACE-WATER; ONLINE PRECONCENTRATION; AQUATIC ENVIRONMENT; QUANTITATIVE-DETERMINATION; MULTIRESIDUE DETERMINATION;
D O I
10.1016/j.chroma.2009.01.097
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An in-line solid-phase extraction-capillary electrophoresis method with UV-vis detection was developed for the monitoring of residues of five sulfonamides (sulfadoxin, sulfadimethoxine, sulfamerazine, sulfachloropyridazine and sulfamethoxazole) in tap, bottled mineral and river waters. For this purpose an analyte concentrator was constructed, based on the introduction of a small portion of a solid-phase extraction sorbent into the electrophoretic capillary to carry out an in-line concentration step, improving sensitivity. A detailed study was carried out to optimize parameters affecting the in-line solid-phase extraction process. such as the design of the concentrator device, type of sorbent and conditions of elution and injection. The proposed method is simple for the environmental monitoring of these antibiotic residues in waters, allowing the direct injection of the samples without any off-line pretreatment and achieving limits of detection between 0.3 and 0.6 mu g/L. Recoveries ranging 52.2-109.2% and relative standard deviations below 13.4% were obtained. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3372 / 3379
页数:8
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