Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS

An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentr...

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Veröffentlicht in:Analytical and bioanalytical chemistry 2021-08, Vol.413 (20), p.5147-5160
Hauptverfasser: Marasco Júnior, César Augusto, da Silva, Bianca Ferreira, Lamarca, Rafaela Silva, de Lima Gomes, Paulo Clairmont Feitosa
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container_issue 20
container_start_page 5147
container_title Analytical and bioanalytical chemistry
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creator Marasco Júnior, César Augusto
da Silva, Bianca Ferreira
Lamarca, Rafaela Silva
de Lima Gomes, Paulo Clairmont Feitosa
description An automated method was developed using on-line solid-phase extraction (SPE) as a sample preparation step, coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS), for determination of pharmaceutical compounds in wastewater samples at nanograms per liter to micrograms per liter concentration levels. This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10 -6 to 1 μg L -1 , while the MQL values were from 0.001 to 3 μg L -1 . Matrix effects were minimized by isotope dilution calibration. Application of the method to 20 wastewater samples showed that caffeine was the most frequently detected compound, with the highest concentration of 715 μg L -1 , while other pharmaceutical compounds were detected in fewer samples and at lower concentrations (up to 8.51 μg L -1 ). Graphical abstract
doi_str_mv 10.1007/s00216-021-03481-7
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This method is suitable for use in routine analysis, especially in environmental applications, avoiding cross-contamination and requiring minimal sample handling. Results can be obtained rapidly, with a chromatographic run time of only 24 min (including sample preparation and chromatographic analysis). Using a 50 μL injection volume, the method was validated according to international guidelines, considering parameters included in terms of method detection (MDL) and quantification limit (MQL), linearity, inter-day and intra-day precisions, and matrix effects. Assessment of chromatographic efficiency considered peak resolution and asymmetry, and carryover was evaluated to ensure analytical reliability and the ability to reuse the SPE cartridge. The intra- and inter-day precisions were lower than 10 and 17%, respectively. The MDL values ranged from 1×10 -6 to 1 μg L -1 , while the MQL values were from 0.001 to 3 μg L -1 . Matrix effects were minimized by isotope dilution calibration. 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subjects Analysis
Analytical Chemistry
Automation
Biochemistry
Caffeine
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Chromatography
Contamination
Dilution
Drugs
Extraction (Chemistry)
Food Science
Ions
Laboratory Medicine
Liquid chromatography
Mass spectrometry
Mass spectroscopy
Methods
Monitoring/Environmental Analysis
Pharmaceuticals
Reliability analysis
Research Paper
Sample preparation
Solid phases
Wastewater
title Automated method to determine pharmaceutical compounds in wastewater using on-line solid-phase extraction coupled to LC-MS/MS
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