Determination of polar organophosphorus pesticides in aqueous samples by direct injection using liquid chromatography-tandem mass spectrometry

被引:103
作者
Ingelse, BA [1 ]
van Dam, RCJ [1 ]
Vreeken, RJ [1 ]
Mol, HGJ [1 ]
Steijger, OM [1 ]
机构
[1] TNO, NL-3700 AJ Zeist, Netherlands
关键词
water analysis; pesticides; organophosphorus compounds;
D O I
10.1016/S0021-9673(01)00660-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It was demonstrated that four out of six of the very polar organophosphorus pesticides (OPs), i.e. acephate, methamidophos, monocrotophos, omethoate, oxydemeton-methyl and vamidothion, could not be extracted from water using commonly available SPE cartridges. Tn addition, GC analysis on all six compounds was found to be troublesome due to their polar and thermolabile character. This initiated the development of an alternative highly sensitive and selective method for the determination of the above mentioned very polar OPs in water, based on LC-MS. Large volume (1 ml) water samples were directly injected onto an RP18 HPLC column with a polar endcapping. The latter was essential for obtaining retention and maintaining colunm performance under 100% aqueous conditions during the sampling. The compounds were ionized using atmospheric pressure chemical ionization and detected on a tandem mass spectrometer operated in multiple reaction-monitoring mode. The detection limits were in the range of 0.01-0.03 mug/l. Compared to conventional GC methods, the developed LC-MS procedure is very straightforward, fast and more reliable. This application demonstrates the applicability of LC-MS for analysis of polar OPs in surface, ground and drinking water, as a more favourable alternative to GC. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:67 / 78
页数:12
相关论文
共 27 条
[1]   Monitoring of pesticides in river water based on samples previously stored in polymeric cartridges followed by on-line solid-phase extraction liquid chromatography diode array detection and confirmation by atmospheric pressure chemical ionization mass spectrometry [J].
Aguilar, C ;
Ferrer, I ;
Borrull, F ;
Marcé, RM ;
Barceló, D .
ANALYTICA CHIMICA ACTA, 1999, 386 (03) :237-248
[2]   Solid phase extraction procedure of polar benzene- and naphthalenesulfonates in industrial effluents followed by unequivocal determination with ion pair chromatography/electrospray-mass spectrometry [J].
Alonso, MC ;
Castillo, M ;
Barceló, D .
ANALYTICAL CHEMISTRY, 1999, 71 (13) :2586-2593
[3]   DETERMINATION OF ACIDIC PESTICIDES IN WATER BY A BENCHTOP ELECTROSPRAY LIQUID-CHROMATOGRAPHY MASS-SPECTROMETER [J].
CRESCENZI, C ;
DICORCIA, A ;
MARCHESE, S ;
SAMPERI, R .
ANALYTICAL CHEMISTRY, 1995, 67 (13) :1968-1975
[4]   Development of a method based on liquid chromatography electrospray mass spectrometry for analyzing imidazolinone herbicides in environmental water at part-per-trillion levels [J].
D'Ascenzo, G ;
Gentili, A ;
Marchese, S ;
Perret, D .
JOURNAL OF CHROMATOGRAPHY A, 1998, 800 (01) :109-119
[5]   GRAPHITIZED CARBON-BLACK EXTRACTION CARTRIDGES FOR MONITORING POLAR PESTICIDES IN WATER [J].
DICORCIA, A ;
SAMPERI, R ;
MARCOMINI, A ;
STELLUTO, S .
ANALYTICAL CHEMISTRY, 1993, 65 (07) :907-912
[6]  
*DIR GEN HLTH CONS, SANCO82500 DIR GEN H
[7]   Comparison of various sample handling and analytical procedures for the monitoring of pesticides and metabolites in ground waters [J].
Fernandez-Alba, AR ;
Agüera, A ;
Contreras, M ;
Peñuela, G ;
Ferrer, I ;
Barceló, D .
JOURNAL OF CHROMATOGRAPHY A, 1998, 823 (1-2) :35-47
[8]   Multiresidue procedures for determination of triazine and organophosphorus pesticides in water by use of large-volume PTV injection in gas chromatography [J].
Forcada, M ;
Beltran, J ;
López, FJ ;
Hernández, F .
CHROMATOGRAPHIA, 2000, 51 (5-6) :362-368
[9]   Reversed-phase ion-pair chromatography coupled to electrospray ionisation mass spectrometry by on-line removal of the counter-ions [J].
Forngren, BH ;
Samskog, J ;
Gustavsson, SÅ ;
Tyrefors, N ;
Markides, KE ;
Långström, B .
JOURNAL OF CHROMATOGRAPHY A, 1999, 854 (1-2) :155-162
[10]  
Hatrik S, 1996, J CHROMATOGR A, V733, P217