期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 409, 期 23, 页码 5441-5450出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-017-0467-7
关键词
Ibuprofen; Carbamazepine; Fish metabolites; Carboxylesterases; Bile; High-resolution mass spectrometry
资金
- EU through the FP7 project GLOBAQUA [603629]
- MEC [NET-SCARCE] [CTM2015-69780-REDC]
- Generalitat de Catalunya [2014 SGR 418]
- MINECO [CTM 2010-16611]
The widespread occurrence of pharmaceuticals in the aquatic environment has raised concerns about potential adverse effects on exposed wildlife. Very little is currently known on exposure levels and clearance mechanisms of drugs in marine fish. Within this context, our research was focused on the identification of main metabolic reactions, generated metabolites, and caused effects after exposure of fish to carbamazepine (CBZ) and ibuprofen (IBU). To this end, juveniles of Solea senegalensis acclimated to two temperature regimes of 15 and 20 A degrees C for 60 days received a single intraperitoneal dose of these drugs. A control group was administered the vehicle (sunflower oil). Bile samples were analyzed by ultra-high-performance liquid chromatography-high-resolution mass spectrometry on a Q Exactive (Orbitrap) system, allowing to propose plausible identities for 11 metabolites of CBZ and 13 metabolites of IBU in fish bile. In case of CBZ metabolites originated from aromatic and benzylic hydroxylation, epoxidation, and ensuing O-glucuronidation, O-methylation of a catechol-like metabolite was also postulated. Ibuprofen, in turn, formed multiple hydroxyl metabolites, O-glucuronides, and (hydroxyl)-acyl glucuronides, in addition to several taurine conjugates. Enzymatic responses after drug exposures revealed a water temperature-dependent induction of microsomal carboxylesterases. The metabolite profiling in fish bile provides an important tool for pharmaceutical exposure assessment.
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