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izvor podataka: crosbi

Simultaneous analysis of opioid analgesics and their metabolites in municipal wastewaters and river water by liquid chromatography–tandem mass spectrometry (CROSBI ID 247062)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Krizman-Matasić, Ivona ; Kostanjevečki, Petra ; Ahel, Marijan ; Terzić, Senka Simultaneous analysis of opioid analgesics and their metabolites in municipal wastewaters and river water by liquid chromatography–tandem mass spectrometry // Journal of Chromatography A, 1533 (2018), 102-111. doi: 10.1016/j.chroma.2017.12.025

Podaci o odgovornosti

Krizman-Matasić, Ivona ; Kostanjevečki, Petra ; Ahel, Marijan ; Terzić, Senka

engleski

Simultaneous analysis of opioid analgesics and their metabolites in municipal wastewaters and river water by liquid chromatography–tandem mass spectrometry

Although published literature provides a clear demonstration of widespread occurrence of opioid analgesics (OAs) in the aquatic environment, analytical methods suitable for a systematic study of this pharmaceutical class, which would include a broad spectrum of opioid analgesics and their metabolites, are still missing. In this work, a comprehensive multiresidue method for quantitative analysis of 27 opioid analgesics and their metabolites, including 2 morphine glucuronide conjugates, was developed and validated for three matrices: raw wastewater (RW), secondary effluent (SE) and river water. The method comprised different classes of opioid analgesics, including natural opiates (morphine and codeine), their semi- synthetic derivatives (hydrocodone, hydromorphone, oxycodone, oxymorphone and buprenorphine) as well as fully synthetic opioids such as methadone, fentanyl, sufentanil, propoxyphene and tramadol. The optimized enrichment procedure involved mixed- mode, strong cation-exchange sorbent in combination with a sequential elution procedure. The extracts were analyzed by reversed-phase liquid chromatography using a Synergy Polar column coupled to electrospray ionization tandem mass spectrometry (LC–MS/MS). Accurate quantification of target OAs was achieved using 19 deuterated analogues as surrogate standards. Method accuracies for RW, SE and river water varied in the range from 91 to 126%, 74 to 120% and 75 to 116%, respectively. Careful optimization of the procedure allowed reliable determination of OAs with method quantification limits in the low ng/L range (RW: 0.3-3.5 ng/L ; SE: 0.2-1.9 ng/L, river water: 0.1-0.8 ng/L. The developed method was applied for analysis of RW, SE and river water samples from Croatia. The concentrations of individual OAs in municipal wastewater varied in a wide range (from < QL to 859 ng/L) and the most prevalent representatives were tramadol, codeine, morphine and methadone and their derivatives. Elevated concentrations of morphine glucuronides (up to 370 ng/L) found in raw municipal wastewater indicated their importance in the overall morphine mass balance.

pharmaceuticals ; opioid analgesics ; liquid chromatography-tandem mass spectrometry ; wastewater ; surface water keywords plus:solid-phase extraction ; urban waste-water ; illicit drugs ; surface waters ; pharmaceuticals ; quantification ; effluents ; abuse ; identification ; contaminants

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Podaci o izdanju

1533

2018.

102-111

objavljeno

0021-9673

1873-3778

10.1016/j.chroma.2017.12.025

Povezanost rada

Biologija, Geologija, Kemija

Poveznice
Indeksiranost