Multi-residue enantioselective determination of emerging drug contaminants in seawater by solid phase extraction and liquid chromatography-tandem mass spectrometry.
McKenzie, Katie; Moffat, Colin F; Petrie, Bruce
Colin F Moffat
This study proposes a new multi-residue enantioselective method for the determination of emerging drug contaminants in sea water by solid phase extraction (SPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). To achieve satisfactory enantiomeric separation with a vancomycin stationary phase it was essential to limit sodium chloride in extracted samples to [less than] 1 µg injection-1. This was achieved through a straightforward SPE method using a 50 mL water wash volume and analyte elution in acetonitrile. A Chiral-V enantioselective column (150 x 2.1mm; 2.7µm particle size) operated in polar ionic mode enabled simultaneous drug separations in 30 minutes. Analytes with enantioresolution E$ were the stimulants amphetamine and methamphetamine, the beta-agonist salbutamol, the beta-blockers propranolol, sotalol and acebutolol, the anti-depressants fluoxetine, venlafaxine, desmethylvenlafaxine and citalopram, and the antihistamine chlorpheniramine. Method quantitation limits were [less than] 10 ng L-1 and method trueness was 80-110% for most analytes. The method was applied to samples from the Forth and Clyde estuaries, Scotland. Chiral drugs were present at concentrations in the range 4-159 ng L-1 and several were in non-racemic form (enantiomeric fraction G 0.50) demonstrating enantiomer enrichment. This emphasises the need for further enantiospecific drug exposure and effect studies in the marine environment.
|Journal Article Type||Article|
|Publisher||Royal Society of Chemistry|
|Peer Reviewed||Peer Reviewed|
|Institution Citation||MCKENZIE, K., MOFFAT, C.F. and PETRIE, B. . Multi-residue enantioselective determination of emerging drug contaminants in seawater by solid phase extraction and liquid chromatography-tandem mass spectrometry. Analytical methods [online], Accepted Manuscripts. Available from: https://doi.org/10.1039/d0ay00801j|
|Keywords||Liquid chromatography; Tandem mass spectrometry; Chiral; Pharmaceutical; Drug|
MCKENZIE 2020 Multi-residue
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