First Evidence for Occurrence of Hydroxylated Human Metabolites of Diclofenac and Aceclofenac in Wastewater Using QqLIT-MS and QqTOF-MS
- 26 September 2008
- journal article
- research article
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 80 (21) , 8135-8145
- https://doi.org/10.1021/ac801167w
Abstract
The two nonsteroidal anti-inflammatory drugs diclofenac (DCF) and aceclofenac (ACF) were monitored for the first time together with their major human phase-I metabolites, namely, 4′-hydroxydiclofenac (4′-OH-DCF) and 4′-hydroxyaceclofenac (4′-OH-ACF), in untreated and treated sewage samples, collected from a municipal wastewater treatment plant which operated a continuous activated sludge (CAS) treatment in parallel with membrane bioreactor (MBR) technology. Mean concentrations of DCF and 4′-OH-DCF in the influent samples amounted to 349 and 237 ng/L, respectively, whereas levels of 4′-OH-ACF (average, 59 ng/L) exceeded those of its parent drug ∼2-fold (31 ng/L). Removal rates of 26 and 56% were achieved for 4′-OH-DCF following CAS and MBR treatment, respectively. The most efficient elimination was observed for 4′-OH-ACF in the MBR with only 4% of the influent concentration remaining in the treated sewage. Biodegradation experiments in batch reactors loaded with mixed liquor demonstrated that ACF underwent rapid ester cleavage to liberate DCF, thus constituting a possible source of DCF release during biological sewage treatment. Studies on the microbial metabolism of DCF (295 Da) in controlled laboratory settings allowed us to identify three novel aerobic biotransformation products. Structure elucidation by means of ultraperformance liquid chromatography-electrospray ionization-hybrid quadrupole-time-of-flight-mass spectrometry in conjunction with H/D-exchange experiments unequivocally identified them as deriving from nitrosation of the hydroxyl group in the carboxylic acid moiety (324 Da) and from nitration of one of the aromatic ring systems (340 Da). A third microbial metabolite emerging in the test medium was assigned as dichlorobenzoic acid (190 Da), possibly formed by N-dealkylation of DCF and subsequent carboxylation. Taken together, this work constitutes the first report on the occurrence of ACF and the human metabolites 4′-OH-DCF and 4′-OH-ACF in wastewater, underpinning the need of incorporating metabolites excreted by humans in monitoring surveys as part of a risk evaluation for environmentally relevant pharmaceuticals.This publication has 35 references indexed in Scilit:
- Isolation and characterization of a new human urinary metabolite of diclofenac applying LC–NMR–MS and high-resolution mass analysesJournal of Pharmaceutical and Biomedical Analysis, 2008
- Simultaneous determination of aceclofenac and its three metabolites in plasma using liquid chromatography–tandem mass spectrometryJournal of Pharmaceutical and Biomedical Analysis, 2008
- Comparison of sulfonated and other micropollutants removal in membrane bioreactor and conventional wastewater treatmentWater Research, 2007
- Acetylation and nitrosation of ciprofloxacin by environmental strains of mycobacteriaCanadian Journal of Microbiology, 2007
- Analysis of pharmaceuticals in wastewater and removal using a membrane bioreactorAnalytical and Bioanalytical Chemistry, 2006
- Transformation of the Antibacterial Agent Norfloxacin by Environmental MycobacteriaApplied and Environmental Microbiology, 2006
- Strategies for characterization of drug metabolites using liquid chromatography–tandem mass spectrometry in conjunction with chemical derivatization and on-line H/D exchange approachesJournal of Pharmaceutical and Biomedical Analysis, 2005
- A multi-centre, double-blind comparative study of the efficacy and safety of aceclofenac and diclofenar in the treatment of rheumatoid arthritisCurrent Medical Research and Opinion, 1995
- Cytochrome P450TB (CYP2C): A major monooxygenase catalyzing diclofenac 4′-hydroxylation in human liverLife Sciences, 1993
- Dissolution and Partition Thermodynamic Functions of Some Nonsteroidal Anti-Inflammatory DrugsJournal of Pharmaceutical Sciences, 1986