Development of fast and robust multiresidual LC-MS/MS method for determination of pharmaceuticals in soils
Language English Country Germany Media print-electronic
Document type Journal Article, Validation Study
PubMed
27044290
DOI
10.1007/s11356-016-6487-6
PII: 10.1007/s11356-016-6487-6
Knihovny.cz E-resources
- Keywords
- Extraction efficiency, Extraction method, Liquid chromatography-tandem mass spectrometry, Matrix effects, Sediments, Sludge, Validation,
- MeSH
- 2-Propanol MeSH
- Acetonitriles MeSH
- Chromatography, Liquid methods MeSH
- Soil Pollutants analysis MeSH
- Pharmaceutical Preparations analysis MeSH
- Environmental Monitoring methods MeSH
- Sewage chemistry MeSH
- Soil chemistry MeSH
- Tandem Mass Spectrometry methods MeSH
- Publication type
- Journal Article MeSH
- Validation Study MeSH
- Names of Substances
- 2-Propanol MeSH
- acetonitrile MeSH Browser
- Acetonitriles MeSH
- Soil Pollutants MeSH
- Pharmaceutical Preparations MeSH
- Sewage MeSH
- Soil MeSH
The aim of this study was to develop a simple extraction procedure and a multiresidual liquid chromatography-tandem mass spectrometry method for determination of a wide range of pharmaceuticals from various soil types. An extraction procedure for 91 pharmaceuticals from 13 soil types, followed by liquid chromatography-tandem mass spectrometry analysis, was optimized. The extraction efficiencies of three solvent mixtures for ultrasonic extraction were evaluated for 91 pharmaceuticals. The best results were obtained using acetonitrile/water (1/1 v/v with 0.1 % formic acid) followed by acetonitrile/2-propanol/water (3/3/4 v/v/v with 0.1 % formic acid) for extracting 63 pharmaceuticals. The method was validated at three fortification levels (10, 100, and 1000 ng/g) in all types of representative soils; recovery of 44 pharmaceuticals ranged between 55 and 135 % across all tested soils. The method was applied to analyze actual environmental samples of sediments, soils, and sludge, and 24 pharmaceuticals were found above limit of quantification with concentrations ranging between 0.83 ng/g (fexofenadine) and 223 ng/g (citalopram).
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