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Advanced oxidation processes on doxycycline degradation: monitoring of antimicrobial activity and toxicity

  • Global toxicity assessment: chemicals, environmental samples, and analytical methods
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Abstract

Advanced oxidation processes (AOPs) have been highly efficient in degrading contaminants of emerging concern (CEC). This study investigated the efficiency of photolysis, peroxidation, photoperoxidation, and ozonation at different pH values to degrade doxycycline (DC) in three aqueous matrices: fountain, tap, and ultrapure water. More than 99.6% of DC degradation resulted from the UV/H2O2 and ozonation processes. Also, to evaluate the toxicity of the original solution and throughout the degradation time, antimicrobial activity tests were conducted using Gram-positive (Bacillus subtilis) and Gram-negative (Escherichia coli) bacteria, and acute toxicity test using the bioluminescent marine bacterium (Vibrio fischeri). Antimicrobial activity reduced as the drug degradation increased in UV/H2O2 and ozonation processes, wherein the first process only 6 min was required to reduce 100% of both bacteria activity. In ozonation, 27.7 mg L−1 of ozone was responsible for reducing 100% of the antimicrobial activity. When applied the photoperoxidation process, an increase in the toxicity occurred as the high levels of degradation were achieved; it means that toxic intermediates were formed. The ozonated solutions did not present toxicity.

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Acknowledgements

The authors gratefully acknowledge CNPq and FAPESP for scholarships granted to M. Spina-Cruz and M.G. Maniero (2013/07817-2), respectively, and the financial support provided by FAPESP (2013/04656-8 and 2013/09543-7) and CNPq (479131/2013-9 and 459078/2014-3).

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Correspondence to José Roberto Guimarães.

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Responsible editor: Vítor Pais Vilar

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Spina-Cruz, M., Maniero, M.G. & Guimarães, J.R. Advanced oxidation processes on doxycycline degradation: monitoring of antimicrobial activity and toxicity. Environ Sci Pollut Res 26, 27604–27619 (2019). https://doi.org/10.1007/s11356-018-2149-1

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  • DOI: https://doi.org/10.1007/s11356-018-2149-1

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