On-line hyphenation of solid-phase extraction to chromatographic separation of sulfonamides with fused-core columns in sequential injection chromatography

被引:31
作者
Batista, Alex D. [1 ]
Chocholous, Petr [2 ]
Satinsky, Dalibor [2 ]
Solich, Petr [2 ]
Rocha, Fabio R. P. [1 ]
机构
[1] Univ Sao Paulo, Ctr Energia Nucl Agr, BR-13400970 Piracicaba, SP, Brazil
[2] Charles Univ Prague, Fac Pharm, Dept Analyt Chem, Hradec Kralove, Czech Republic
基金
巴西圣保罗研究基金会;
关键词
SPE-SIC; Sequential Injection Chromatography; Pentafluorophenylpropyl; F5; Fused core; Sulfonamides; On-line SPE; Anion-exchange; PERFORMANCE LIQUID-CHROMATOGRAPHY; CAPILLARY-ZONE-ELECTROPHORESIS; MASS-SPECTROMETRY; ENVIRONMENTAL WATERS; SAMPLE PREPARATION; WASTE-WATER; ANTIBIOTICS; MICROEXTRACTION; METABOLITES; URINE;
D O I
10.1016/j.talanta.2014.07.056
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
On-line sample pretreatment (clean-up and analyte preconcentration) is for the first time coupled to sequential injection chromatography. The approach combines anion-exchange solid-phase extraction and the highly effective pentafluorophenylpropyl (F5) fused-core particle column for separation of eight sulfonamide antibiotics with similar structures (sulfathiazole, sulfanilamide, sulfacetamide, sulfadiazine, sulfamerazine, sulfadimidine, sulfamethoxazole and sulfadimethoxine). The stationary phase was selected after a critical comparison of the performance achieved by three fused-core reversed phase columns (Ascentis (R) Express RP-Amide, Phenyl-Hexyl, and F5) and two monolithic columns (Chromolith (R) High Resolution RP-18 and CN). Acetonitrile and acetate buffer pH 5.0 at 0.60 mL min(-1) were used as mobile phase to perform the separations before spectrophotometric detection. The first mobile phase was successfully used as eluent from SPE column ensuring transfer of a narrow zone to the chromatographic column. Enrichment factors up to 39.2 were achieved with a 500 mu L sample volume. The developed procedure showed analysis time < 10.5 min, resolutions > 1.83 with peak symmetry <= 1.52, LODs between 4.9 and 27 mu g L-1, linear response ranges from 30.0 to 1000.0 mu g L-1 (r(2) > 0.996) and RSDs of peak heights <2.9% (n=6) at a 100 mu g L-1 level and enabled the screening control of freshwater samples contaminated at the 100 mu g L-1 level. The proposed approach expanded the analytical potentiality of SIC and avoided the time-consuming batch sample pretreatment step, thus minimizing risks of sample contamination and analyte losses. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 149
页数:8
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