Hydroxyl radical induced degradation of ibuprofen

Sci Total Environ. 2013 Mar 1:447:286-92. doi: 10.1016/j.scitotenv.2013.01.007. Epub 2013 Feb 11.

Abstract

Pulse radiolysis experiments were used to characterize the intermediates formed from ibuprofen during electron beam irradiation in a solution of 0.1mmoldm(-3). For end product characterization (60)Co γ-irradiation was used and the samples were evaluated either by taking their UV-vis spectra or by HPLC with UV or MS detection. The reactions of OH resulted in hydroxycyclohexadienyl type radical intermediates. The intermediates produced in further reactions hydroxylated the derivatives of ibuprofen as final products. The hydrated electron attacked the carboxyl group. Ibuprofen degradation is more efficient under oxidative conditions than under reductive conditions. The ecotoxicity of the solution was monitored by Daphnia magna standard microbiotest and Vibrio fischeri luminescent bacteria test. The toxic effect of the aerated ibuprofen solution first increased upon irradiation indicating a higher toxicity of the first degradation products, then decreased with increasing absorbed dose.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aliivibrio fischeri / drug effects
  • Animals
  • Chromatography, High Pressure Liquid
  • Daphnia / drug effects
  • Ecotoxicology / methods
  • Gamma Rays
  • Hydroxyl Radical / chemistry*
  • Hydroxylation
  • Ibuprofen / chemistry*
  • Ibuprofen / radiation effects
  • Ibuprofen / toxicity
  • Luminescence
  • Mass Spectrometry
  • Pulse Radiolysis
  • Solutions / toxicity
  • Spectrophotometry, Ultraviolet
  • Water Pollutants, Chemical / chemistry*
  • Water Pollutants, Chemical / toxicity

Substances

  • Solutions
  • Water Pollutants, Chemical
  • Hydroxyl Radical
  • Ibuprofen