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Analytical method development for the determination of emerging contaminants in water using supercritical-fluid chromatography coupled with diode-array detection
被引:17
|作者:
del Carmen Salvatierra-Stamp, Vilma
[1
]
Ceballos-Magana, Silvia G.
[2
]
Gonzalez, Jorge
[1
]
Ibarra-Galvan, Valentin
[1
]
Muniz-Valencia, Roberto
[1
]
机构:
[1] Univ Colima, Fac Ciencias Quim, Coquimatlan 28400, Colima, Mexico
[2] Univ Colima, Fac Ciencias, Colima 28045, Mexico
关键词:
Emerging contaminants;
Supercritical-fluid chromatography;
Solid-phase extraction;
Environmental water samples;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
SOLID-PHASE EXTRACTION;
TANDEM MASS-SPECTROMETRY;
WASTE-WATER;
SAMPLES;
D O I:
10.1007/s00216-015-8581-x
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
An analytical method using supercritical-fluid chromatography coupled with diode-array detection for the determination of seven emerging contaminants-two pharmaceuticals (carbamazepine and glyburide), three endocrine disruptors (17 alpha-ethinyl estradiol, bisphenol A, and 17 beta-estradiol), one bactericide (triclosan), and one pesticide (diuron)-was developed and validated. These contaminants were chosen because of their frequency of use and their toxic effects on both humans and the environment. The optimized chromatographic separation on a Viridis BEH 2-EP column achieved baseline resolution for all compounds in less than 10 min. This separation was applied to environmental water samples after sample preparation. The optimized sample treatment involved a preconcentration step by means of solid-phase extraction using C18-OH cartridges. The proposed method was validated, finding recoveries higher than 94 % and limits of detection and limits of quantification in the range of 0.10-1.59 mu g L-1 and 0.31-4.83 mu g L-1, respectively. Method validation established the proposed method to be selective, linear, accurate, and precise. Finally, the method was successfully applied to environmental water samples.
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页码:4219 / 4226
页数:8
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