Determination of dichloroanilines in human urine by GC–MS, GC–MS–MS, and GC–ECD as markers of low-level pesticide exposure
| Autor: | J Begerow, H Hajimiragha, L Dunemann, K Wittke |
|---|---|
| Rok vydání: | 2001 |
| Předmět: |
Urine
Propanil Mass spectrometry Sensitivity and Specificity Gas Chromatography-Mass Spectrometry Bridged Bicyclo Compounds chemistry.chemical_compound Animals Humans Linuron Oxazoles Detection limit Aniline Compounds Chromatography Molecular Structure Herbicides Chemistry Hydantoins Phenylurea Compounds Environmental Exposure General Chemistry Aminoimidazole Carboxamide Fungicides Industrial Electron capture detector Diuron Cattle Procymidone Gas chromatography Gas chromatography–mass spectrometry Quantitative analysis (chemistry) Biomarkers |
| Zdroj: | Journal of Chromatography B: Biomedical Sciences and Applications. 755:215-228 |
| ISSN: | 0378-4347 |
| DOI: | 10.1016/s0378-4347(01)00078-0 |
| Popis: | Methods for the determination of 3,4-dichloroaniline (3,4-DCA) and 3,5-dichloroaniline (3,5-DCA) as common markers of eight non-persistent pesticides in human urine are presented. 3,5-DCA is a marker for the exposure to the fungicides vinclozolin, procymidone, iprodione, and chlozolinate. Furthermore the herbicides diuron, linuron, neburon, and propanil are covered using their common marker 3,4-DCA. The urine samples were treated by basic hydrolysis to degrade all pesticides, metabolites, and their conjugates containing the intact moieties completely to the corresponding dichloroanilines. After addition of the internal standard 4-chloro-2-methylaniline, simultaneous steam distillation extraction (SDE) followed by liquid-liquid extraction (LLE) was carried out to produce, concentrate and purify the dichloroaniline moieties. Gas chromatography (GC) with mass spectrometric (MS) and tandem mass spectrometric (MS-MS) detection and also detection with an electron-capture detector (ECD) after derivatisation with heptafluorobutyric anhydride (HFBA) were employed for separation, detection, and identification. Limit of detection of the GC-MS-MS and the GC-ECD methods was 0.03 and 0.05 microg/l, respectively. Absolute recoveries obtained from a urine sample spiked with the internal standard, 3,5-, and 3,4-DCA, ranged from 93 to 103% with 9-18% coefficient of variation. The three detection techniques were compared concerning their performance, expenditure and suitability for their application in human biomonitoring studies. The described procedure has been successfully applied for the determination of 3,4- and 3,5-DCA in the urine of nonoccupationally exposed volunteers. The 3,4-DCA levels in these urine samples ranged between 0.13 and 0.34 microg/g creatinine or 0.11 and 0.56 microg/l, while those for 3,5-DCA were between 0.39 and 3.33 microg/g creatinine or 0.17 and 1.17 microg/l. |
| Databáze: | OpenAIRE |
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