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Journal of Chromatography A
Volume 1124, Issues 1-2, 18 August 2006, Pages 68-81
ExTech 2006 - 8th International Symposium on Advances in Extraction Techniques
 
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doi:10.1016/j.chroma.2006.05.024    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2006 Elsevier B.V. All rights reserved.

Multi-residue analysis of pharmaceuticals in wastewater by ultra-performance liquid chromatography–quadrupole–time-of-flight mass spectrometry

Mira Petrovica, b, Corresponding Author Contact Information, E-mail The Corresponding Author, Meritxell Grosb and Damia Barcelob

aCatalan Institution for Research and Advanced Studies (ICREA), Passeig Lluis Companys 23, 08010 Barcelona, Spain bIIQAB-CSIC, Department of Environmental Chemistry, Jordi Girona 18-26, 08034 Barcelona, Spain

Available online 6 June 2006.

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Abstract

In this work, a new multi-residue method using ultra-performance liquid chromatography (UPLC) quadrupole-time-of-flight mass spectrometry (Q–TOF–MS) was developed for screening and confirmation of 29 pharmaceutical compounds belonging to different therapeutical classes: analgesics and antiinflammatories, lipid regulating agents cholesterol lowering statin agents, psychiatric drugs, anti ulcer agents, histamine H2 receptor antagonist, antibiotics and beta-blockers. UPLC uses columns packed with 1.7 μm particles and enables elution of sample components in much narrower, more concentrated bands, resulting in better chromatographic resolution and increased peak height. The typical peak width was 5–10 s at base, permitting very good separation of all compounds in 10 min, which represented an approximate three-fold reduction in the analysis time in comparison to conventional high-performance liquid chromatography (HPLC). Unequivocal identification of target pharmaceutical compounds was based on accurate mass measurement of the molecular ions in the TOF mode and by performing collision induced dissociation (CID) in the Q–TOF mode in order to generate accurate mass measurement of the product ions. Using lock mass correction the accurate masses calculated for the product ions deviated from the theoretical masses by 0.2 to 1.3 mDa (root mean square (RMS) value = 0.67) and 0.7–6.4 ppm (RMS = 3.53), respectively. Quantitation was carried out working in the TOF mode using the narrow window extracted ion chromatograms (nwXICs) of each compound (extracted using a 20 mDa window) yielding relative standard deviation (RSD) from 0.5 to 5.3% (run-to-run) and from 2.1 to 9.1% (day-to-day) and instrumental detection limits (IDLs) from 1 to 200 pg. Analysis of wastewater treatment plant (WWTP) samples gave method detection limits (MDLs) ranging from 10 to 500 ng/L. The UPLC–Q–TOF method was successfully applied to analyze pharmaceutical residues in WWTP samples.

Keywords: Quadrupole–time-of-flight mass spectrometry; Pharmaceuticals; Environmental analysis; Ultra-performance liquid chromatography

Article Outline

1. Introduction
2. Experimental
2.1. Chemicals and reagents
2.2. UPLC–Q–TOF
2.3. Sample preparation
2.4. Validation of the analytical procedure
3. Results and discussion
3.1. Performance of UPLC
3.2. Q–TOF screening and confirmation
3.3. Quantitative analysis
3.4. Matrix effect in UPLC-Q–TOF
3.5. Analysis of real wastewater samples
4. Conclusions
Acknowledgements
References






Journal of Chromatography A
Volume 1124, Issues 1-2, 18 August 2006, Pages 68-81
ExTech 2006 - 8th International Symposium on Advances in Extraction Techniques
 
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