Study of different atmospheric-pressure interfaces for LC-MS/MS determination of acrylamide in water at sub-ppb levels

被引:24
作者
Marin, Jose M. [1 ]
Pozo, Oscar J. [1 ]
Sancho, Juan V. [1 ]
Pitarch, Elena [1 ]
Lopez, Francisco J. [1 ]
Hernandez, Felix [1 ]
机构
[1] Univ Jaume 1, Res Inst Pesticides & Water, E-12071 Castellon, Spain
来源
JOURNAL OF MASS SPECTROMETRY | 2006年 / 41卷 / 08期
关键词
atmospheric-pressure interfaces; liquid chromatography; tandem mass spectrometry; acrylamide; water;
D O I
10.1002/jms.1063
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid, sensitive and selective method based on LC-MS/MS has been developed for the direct determination of acrylamide residues in water in compliance with the current European Union (EU) 98/83 Drinking Water Directive. Given the high polarity of acrylamide, the application of a rapid on-line solid phase extraction step, commonly used for preconcentrating low analyte levels, was not found to be completely satisfactory. Therefore, an alternative approach based on the use of direct large-volume injection into the LC-MS/MS system has been used. Three atmospheric-pressure interfaces (ESI, APCI and Ion Sabre APCI) were checked to reach the required sensitivity (0.1 mu g/l). All three interfaces were tested by analysis of six different water samples (surface water, groundwater, drinking water and three treated water samples) spiked at three concentration levels each (0.1, 1 and 10 mu g/l). When using ESI, poor sensitivity and high matrix effects were observed. This situation improved when APCI was used as the interface because no matrix effect was found, although sensitivity was not completely satisfactory. The best results were obtained by interfacing the Ion Sabre APCI; its higher sensitivity for acrylamide (LOD 0.03 mu g/l) and the absence of matrix effects recommended its selection. Using this approach, satisfactory recoveries (90-97%) and precision (< 12%) were obtained for all water samples studied. Besides, the acquisition of two different MS/MS transitions allowed not only the quantification but also the confirmation of acrylamide in water at concentration levels around 0.1 mu g/l. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1041 / 1048
页数:8
相关论文
共 24 条
[1]  
Castle L, 2005, J AOAC INT, V88, P274
[2]   Determination of acrylamide in drinking water by large-volume direct injection and ion-exclusion chromatography-mass spectrometry [J].
Cavalli, S ;
Polesello, S ;
Saccani, G .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1039 (1-2) :155-159
[3]  
*EUR COUNC, 1998, 9883EC EU
[4]  
*EUR UN, 2002, 2002657EC EUR UN
[5]   Evaluation of different quantitative approaches for the determination of noneasily ionizable molecules by different atmospheric pressure interfaces used in liquid chromatography tandem mass spectrometry:: Abamectin as case of study [J].
Grimalt, S ;
Pozo, OJ ;
Marín, JM ;
Sancho, JV ;
Hernández, F .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2005, 16 (10) :1619-1630
[6]   Strategies for quantification and confirmation of multi-class polar pesticides and transformation products in water by LC-MS2 using triple quadrupole and hybrid quadrupole time-of-flight analyzers [J].
Hernández, F ;
Pozo, OJ ;
Sancho, JV ;
López, FJ ;
Marín, JM ;
Ibáñez, M .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2005, 24 (07) :596-612
[7]   Comparison of different mass spectrometric techniques combined with liquid chromatography for confirmation of pesticides in environmental water based on the use of identification points [J].
Hernández, F ;
Ibáñez, M ;
Sancho, JV ;
Pozo, OJ .
ANALYTICAL CHEMISTRY, 2004, 76 (15) :4349-4357
[8]  
International Agency for Research on Cancer, 1994, MOM EV CARC RISKS HU, P389
[9]  
Jemal M, 1999, RAPID COMMUN MASS SP, V13, P61, DOI 10.1002/(SICI)1097-0231(19990115)13:1<61::AID-RCM451>3.0.CO
[10]  
2-2