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Determination of 5-fluorocytosine, 5-fluorouracil, and 5-fluorouridine in hospital wastewater by liquid chromatography-mass spectrometry
P. Škvára, S. Santana-Viera, S. Montesdeoca-Esponda, E. Mordačíková, JJ. Santana-Rodríguez, A. Vojs Staňová
Language English Country Germany
Document type Journal Article
Grant support
APVV-16-0124
Slovak Research and Development Agency
UK/193/2018
Comenius University
Spanish Ministry of Economy
CTM2015-66095-C2-1-R
Industry and Competitiveness
LM2018099
Ministry of Education, Youth and Sports of the Czech Republic
- MeSH
- Water Pollutants, Chemical analysis MeSH
- Solid Phase Extraction MeSH
- Flucytosine analysis MeSH
- Fluorouracil analysis MeSH
- Molecular Structure MeSH
- Hospitals * MeSH
- Wastewater chemistry MeSH
- Tandem Mass Spectrometry MeSH
- Uridine analogs & derivatives analysis MeSH
- Chromatography, High Pressure Liquid MeSH
- Publication type
- Journal Article MeSH
Chemotherapeutics are pharmaceutical compounds the occurrence of which in the environment is of growing concern because of the increase in treatments against cancer diseases. They can reach the aquatic ecosystems after passing through wastewater treatment plants without complete removal. One of the most frequently used chemotherapeutics is 5-fluorouracil which exhibits a strong cytostatic effect. In this paper, an analytical methodology was developed, validated, and applied to determine 5-fluorouracil, its precursor, 5-fluorocytosine, and its major active metabolite, 5-fluorouridine, in hospital wastewater samples. Due to the expected low concentrations after dilution and interferences present in such a complex matrix, a very selective and sensitive detection method is required. Moreover, an extraction method must be implemented prior to the determination in order to purify the sample extract and preconcentrate the target analytes at micrograms per liter concentration levels. Solid-phase extraction followed by liquid chromatography with tandem mass spectrometry was the combination of choice and all included parameters were studied. Under optimized conditions for wastewater samples analysis, recoveries from 63 to 108% were obtained, while intraday and interday relative standard deviations never exceeded 20 and 25%, respectively. Limits of detection between 61 and 620 ng/L were achieved. Finally, the optimized method was applied to samples from hospital wastewater effluents.
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