Related Experiment Video
Updated: Jun 20, 2026

High-throughput and Comprehensive Drug Surveillance Using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry
Published on: April 23, 2019
Characterization of Ozonation Transformation Products of Flutamide and Azathioprine by UHPLC-Ion
Josep García-Martínez1, Cristina Corpa2, Guillermo Nieto2
1Department of Chemistry, Centre for Analysis and Synthesis, Lund University, P.O. Box 124, Lund 22100, Sweden.
Abstract:
Ozonation is one of the most promising advanced oxidation processes to be implemented as quaternary treatment for the removal of micropollutants in wastewater treatment plants. However, there are some knowledge gaps that limit its implementation. First, the removal efficiency is not known for all pollutants, and second, knowledge about degradation byproducts is limited, as well as the toxicity of the treated waters. In this work, the removal efficiency of azathioprine and flutamide is studied, as well as the transformation products formed during ozonation. A lab-scale reactor was used for ozonation of the drugs in pure water, with ambient air as the source for ozone generation and liquid chromatography-ion mobility-high-resolution mass spectrometry for time-resolved process monitoring. Notably, azathioprine and flutamide were not completely removed by ozonation, with 49-54% remaining after the treatment. Furthermore, two transformation products of azathioprine and three of flutamide were identified, including previously unreported nitroaromatic transformation products of flutamide. While both parent compounds showed relatively low predicted toxicity, transformation products of flutamide exhibited higher predicted chronic toxicity. These results highlight the importance of considering transformation products during ozonation and suggest possible nitration reactions when ozone is generated from ambient air. Further experiments are needed to confirm this.
More Related Videos
05:46Identification of Pharmaceuticals in The Aquatic Environment Using HPLC-ESI-Q-TOF-MS and Elimination of Erythromycin Through Photo-Induced Degradation
Published on: August 1, 2018
11:00Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry (UPLC-HRMS)
Published on: May 20, 2013
Related Concept Videos
Mass Spectrometry: Aromatic Compound Fragmentation
Phase I Reactions: Oxidation of Aliphatic and Aromatic Carbon-Containing Systems
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
Atomic Fluorescence Spectroscopy