4.6 Article

Enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1218, 期 29, 页码 4746-4754

出版社

ELSEVIER
DOI: 10.1016/j.chroma.2011.05.046

关键词

2-Arylpropionic acids; Non-steroidal anti-inflammatory drugs (NSAIDs); Enantiomeric fraction; Chiral analysis; Profens

资金

  1. Australian Research Council (ARC) [DP0772864]
  2. Ministry of Higher Education, Malaysia
  3. Australian Research Council [DP0772864] Funding Source: Australian Research Council

向作者/读者索取更多资源

A highly sensitive and reliable method for the enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples has been developed. These three pharmaceuticals are chiral molecules and the variable presence of their individual (R)- and (S)-enantiomers is of increasing interest for environmental analysis. An indirect method for enantioseparation was achieved by the derivatization of the (R)- and (S)-enantiomers to amide diastereomers using (R)-1-phenylethylamine ((R)-1-PEA). After initial solid phase extraction from aqueous samples, derivatization was undertaken at room temperature in less than 5 min. Optimum recovery and clean-up of the amide diastereomers from the derivatization solution was achieved by a second solid phase extraction step. Separation and detection of the individual diastereomers was undertaken by gas chromatography-tandem mass spectrometry (GC-MS/MS). Excellent analyte separation and peak shapes were achieved for the derivatized (R)- and (S)-enantiomers for all three pharmaceuticals with peak resolution. R-s is in the range of 2.87-4.02 for all diastereomer pairs. Furthermore, the calibration curves developed for the (S)-enantiomers revealed excellent linearity (r(2) >= 0.99) for all three compounds. Method detection limits were shown to be within the range of 0.2-3.3 ng L-1 for individual enantiomers in ultrapure water, drinking water, surface water and a synthetic wastewater. Finally, the method was shown to perform well on a real tertiary treated wastewater sample, revealing measurable concentrations of both (R)- and (S)-enantiomers of ibuprofen, naproxen and ketoprofen. Isotope dilution using racemic D-3-ibuprofen, racemic D-3-ketoprofen and racemic D-3-naproxen was shown to be an essential aspect of this method for accurate quantification and enantiomeric fraction (EF) determination. This approach produced excellent reproducibility for EF determination of triplicate tertiary treated wastewater samples. (C) 2011 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据