Trace analysis of fluoxetine and its metabolite norfluoxetine. Part II: Enantioselective quantification and studies of matrix effects in raw and treated wastewater by solid phase extraction and liquid chromatography-tandem mass spectrometry

被引:37
作者
Barclay, Victoria K. H. [1 ]
Tyrefors, Niklas L. [1 ]
Johansson, I. Monika [1 ,2 ]
Pettersson, Curt E. [1 ]
机构
[1] Uppsala Univ, Div Analyt Pharmaceut Chem, SE-75123 Uppsala, Sweden
[2] Med Prod Agcy, SE-75103 Uppsala, Sweden
关键词
Matrix effects; LC-MS/MS; Chiral analysis; Wastewater; Isotope-labeled compound; Fluoxetine and norfluoxetine; SEROTONIN REUPTAKE INHIBITORS; SURFACE WATERS; ELECTROSPRAY-IONIZATION; PHARMACEUTICAL RESIDUES; HUMAN PLASMA; SEWAGE; SUPPRESSION; ENVIRONMENT; ENANTIOMERS; ASSAYS;
D O I
10.1016/j.chroma.2011.12.084
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
The isotope-labeled compounds fluoxetine-d(5) and norfluoxetine-d(5) were used to study matrix effects caused by co-eluting compounds originating from raw and treated wastewater samples, collected in Uppsala, Sweden. The matrix effects were investigated by the determination of matrix factors (MF) and by a post-column infusion method. The matrix factors were determined to be 38-47% and 71-86% for the enantiomers of norfluoxetine-d(5) and fluoxetine-d(5), respectively. The influence of matrix effects when quantifying the enantiomers of the active pharmaceutical ingredient and the metabolite in wastewater samples with LC-MS/MS is discussed and methods to overcome the problem are presented. The enantiomeric concentrations of fluoxetine and its human metabolite norfluoxetine, quantified by a one-point calibration method, were 12-52 pM (3.5-16 ng L-1) in raw wastewater and 4-48 pM (1.2-15 ng L-1) in treated wastewater. Furthermore, the calculated enantiomeric fractions (EF) of the substances were found to be between 0.68 and 0.71 in both matrices. Neither the EF values for fluoxetine nor those for norfluoxetine were significantly different in the raw wastewater compared to the treated wastewater. Interestingly, the concentration of (S)-fluoxetine was found to be higher than the concentration of (R)fluoxetine in both raw and treated wastewater. These results are different from other results presented in the literature, which shows that the relative concentrations of the enantiomers of a chiral active pharmaceutical ingredient might be significantly different in wastewater samples from different treatment systems. We report, for the first time, the concentrations of the enantiomers of norfluoxetine in wastewater samples. The concentrations of (S)-norfluoxetine were found to be higher than the concentration of (R)-norfluoxetine in the raw as well as in the treated wastewater samples. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 114
页数:10
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