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Enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples.
J Chromatogr A. 2011 Jul 22; 1218(29):4746-54.JC

Abstract

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.

Authors+Show Affiliations

UNSW Water Research Centre, School of Civil and Environmental Engineering, University of New South Wales, Sydney, Australia. nor.hashim@student.unsw.edu.auNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21645900

Citation

Hashim, Nor H., and Stuart J. Khan. "Enantioselective Analysis of Ibuprofen, Ketoprofen and Naproxen in Wastewater and Environmental Water Samples." Journal of Chromatography. A, vol. 1218, no. 29, 2011, pp. 4746-54.
Hashim NH, Khan SJ. Enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples. J Chromatogr A. 2011;1218(29):4746-54.
Hashim, N. H., & Khan, S. J. (2011). Enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples. Journal of Chromatography. A, 1218(29), 4746-54. https://doi.org/10.1016/j.chroma.2011.05.046
Hashim NH, Khan SJ. Enantioselective Analysis of Ibuprofen, Ketoprofen and Naproxen in Wastewater and Environmental Water Samples. J Chromatogr A. 2011 Jul 22;1218(29):4746-54. PubMed PMID: 21645900.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective analysis of ibuprofen, ketoprofen and naproxen in wastewater and environmental water samples. AU - Hashim,Nor H, AU - Khan,Stuart J, Y1 - 2011/05/20/ PY - 2010/11/08/received PY - 2011/02/08/revised PY - 2011/05/12/accepted PY - 2011/6/8/entrez PY - 2011/6/8/pubmed PY - 2011/9/21/medline SP - 4746 EP - 54 JF - Journal of chromatography. A JO - J Chromatogr A VL - 1218 IS - 29 N2 - 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. SN - 1873-3778 UR - https://www.unboundmedicine.com/medline/citation/21645900/Enantioselective_analysis_of_ibuprofen_ketoprofen_and_naproxen_in_wastewater_and_environmental_water_samples_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0021-9673(11)00688-1 DB - PRIME DP - Unbound Medicine ER -