Fully automated online solid phase extraction coupled directly to liquid chromatography-tandem mass spectrometry - Quantification of sulfonamide antibiotics, neutral and acidic pesticides at low concentrations in surface waters

被引:159
作者
Stoob, K
Singer, HP
Goetz, CW
Ruff, M
Mueller, SR
机构
[1] Swiss Fed Inst Aquat Sci & Technol, Eawag Water & Agr Dept, CH-8600 Dubendorf, Switzerland
[2] Swiss Fed Inst Technol, ETH, Zurich, Switzerland
关键词
fully automated online extraction; acetyl sulfonamide antibiotics; sulcotrione; mesotrione; ESA OXA metabolites; biocides;
D O I
10.1016/j.chroma.2005.08.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fully automated online solid phase extraction-liquid chromatography-tandem mass spectrometry (SPE-LC-MS/MS) instrumental setup has been developed for the quantification of sulfonamide antibiotics and pesticides in natural water. The direct coupling of an online solid phase extraction cartridge (Oasis HLB) to LC-MS/MS was accomplished using column switching techniques. High sensitivity in the low ng/L range was achieved by large volume injections of 18 mL with a combination of a tri-directional autosampler and a dispenser system. This setup allowed high sample throughput with a minimum of investment costs. Special emphasis was placed on low cross contamination. The chosen approach is suitable for research as well as for monitoring applications. The flexible instrumental setup was successfully optimised for different important groups of bioactive chemicals resulting in three trace analytical methods for quantification of (i) sulfonamide antibiotics and their acetyl metabolites; (ii) neutral pesticides (triazines, phenylureas, amides, chloracetanilides) and (iii) acidic pesticides (phenoxyacetic acids and triketones). Absolute extraction recoveries from 85 to 112% were obtained for the different analytes. More than 500 samples could be analyzed with one extraction cartridge. The inter-day precision of the method was excellent indicated by relative standard deviations between 1 and 6%. High accuracy was achieved by the developed methods resulting in maximum deviation relative to the spiked amount of 8-15% for the different analytes. Detection limits for various environmental samples were between 0.5 and 5 ng/L. Matrix induced ion suppression was in general smaller than 25%. The performance of the online methods was demonstrated with measurements of concentration dynamics of sulfonamide antibiotics and pesticides concentrations in a little creek during rain fall events. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 147
页数:10
相关论文
共 43 条
[1]   Trace determination of priority pesticides in water by means of high-speed on-line solid-phase extraction-liquid chromatography-tandem mass spectrometry using turbulent-flow chromatography columns for enrichment and a short monolithic column for fast liquid chromatographic separation [J].
Asperger, A ;
Efer, J ;
Koal, T ;
Engewald, W .
JOURNAL OF CHROMATOGRAPHY A, 2002, 960 (1-2) :109-119
[2]   Simultaneous analysis of multiple classes of antibiotics by ion trap LC/MS/MS for assessing surface water and groundwater contamination [J].
Batt, AL ;
Aga, DS .
ANALYTICAL CHEMISTRY, 2005, 77 (09) :2940-2947
[3]   Veterinary medicines in the environment [J].
Boxall, ABA ;
Fogg, LA ;
Blackwell, PA ;
Kay, P ;
Pemberton, EJ ;
Croxford, A .
REVIEWS OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, VOL 180, 2004, 180 :1-91
[4]   Simultaneous determination of neutral and acidic pesticides in natural waters at the low nanogram per liter level [J].
Bucheli, TD ;
Gruebler, FC ;
Muller, SR ;
Schwarzenbach, RP .
ANALYTICAL CHEMISTRY, 1997, 69 (08) :1569-1576
[5]   Spherical clay conglomerates:: A novel stationary phase for solid phase extraction and "reversed-phase" liquid chromatography [J].
Bucheli, TD ;
Müller, SR ;
Reichmuth, P ;
Haderlein, SB ;
Schwarzenbach, RP .
ANALYTICAL CHEMISTRY, 1999, 71 (11) :2171-2178
[6]   Strategic survey of therapeutic drugs in the rivers Po and Lambro in northern Italy [J].
Calamari, D ;
Zuccato, E ;
Castiglioni, S ;
Bagnati, R ;
Fanelli, R .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (07) :1241-1248
[7]   New hydrophilic materials for solid-phase extraction [J].
Fontanals, N ;
Marcé, RM ;
Borrull, F .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2005, 24 (05) :394-406
[8]   Quantification of the new triketone herbicides, sulcotrione and mesotrione, and other important herbicides and metabolites, at the ng/l level in surface waters using liquid chromatography-tandem mass spectrometry [J].
Freitas, LG ;
Götz, CW ;
Ruff, M ;
Singer, HP ;
Müller, SR .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (02) :277-286
[9]   Determination of polar pesticides with atmospheric pressure chemical ionisation mass spectrometry-mass spectrometry using methanol and/or acetonitrile for solid-phase desorption and gradient liquid chromatography [J].
Geerdink, RB ;
Kooistra-Sijpersma, A ;
Tiesnitsch, J ;
Kienhuis, PGM ;
Brinkman, UAT .
JOURNAL OF CHROMATOGRAPHY A, 1999, 863 (02) :147-155
[10]   Determination of phenylurea herbicides in natural waters at concentrations below 1 ng 1-1 using solid-phase extraction, derivatization, and solid-phase microextraction gas chromatography mass spectrometry [J].
Gerecke, AC ;
Tixier, C ;
Bartels, T ;
Schwarzenbach, RP ;
Müller, SR .
JOURNAL OF CHROMATOGRAPHY A, 2001, 930 (1-2) :9-19