Exploring the aquatic photodegradation of two ionisable fluoroquinolone antibiotics – Gatifloxacin and balofloxacin: Degradation kinetics, photobyproducts and risk to the aquatic environment
Creators
- 1. Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ (United Kingdom)
- 2. Key Laboratory for Ecological Environment in Coastal Areas (SOA), National Marine Environmental Monitoring Center, Dalian 116023 (China)
- 3. The Environmental Research Institute, MOE Key Laboratory of Environmental Theoretical Chemistry, South China Normal University, Guangzhou 510006 (China)
Description
Highlights: • Distinct photochemistry of two dissociated FQs (H2FQs+, HFQs0 and FQs−) was reported. • HFQs0 had the highest apparent photolytic efficiency and ·OH oxidation reactivity. • Relevance and pathways of these reactions were clarified based on key photoproducts. • Antibacterial activity of GAT to E. coli. persisted even after notable photolysis. Fluoroquinolone antibiotics (FQs) are ubiquitous and ionisable in surface waters. Here we investigate gatifloxacin (GAT) and balofloxacin (BAL), two widely used FQs, and determine the photochemical reactivity of their respective dissociation species that arise at different pH to understand the relevance and pathways of phototransformation reactions. Simulated-sunlight experiments and matrix calculations showed that neutral forms (HFQs0) of the two antibiotics had the highest apparent photolytic efficiency and hydroxyl-radical oxidation reactivity. Based on the pH-dependent photochemical reactivities, the solar apparent photodegradation half-lives (t1/2) in sunlit surface waters ranged from 14.5–169 min and was 1–2 orders of magnitude faster than hydroxyl-radical induced oxidation (t1/2 = 20.9–29.8 h). The corresponding pathways were proposed based on the identification of key intermediates using HPLC-ESI-MS/MS. The apparent photodegradation induced defluorination, decarboxylation, and piperazinyl oxidation and rearrangement, whereas hydroxyl-radical oxidation caused hydroxylated defluorination and piperazinyl hydroxylation. The photomodified toxicity of GAT and BAL was examined using an Escherichia coli activity assay. E. coli activity was not affected by BAL, but was significantly affected by the photo-modified solutions of GAT, indicating that primary photo-degradates have a comparable or higher antibacterial activity than the parent GAT. In fresh water and seawater this antibacterial activity remained high for up to 24 h, even after GAT had undergone significant photodegradation (>1 half-life), indicating the potential impact of this chemical on microbial communities in aquatic systems.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2018.03.279Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2018.03.279;
- PII
- S0048969718310386;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 633
- Journal Page Range
- p. 1192-1197
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53026536
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ANTIBIOTICS; AQUATIC ECOSYSTEMS; DECARBOXYLATION; DISSOCIATION; ESCHERICHIA COLI; FRESH WATER; HAZARDS; HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROXYL RADICALS; HYDROXYLATION; OXIDATION; PH VALUE; PHOTOCHEMISTRY; PHOTOLYSIS; SEAWATER; SIMULATION; SURFACE WATERS; TOXICITY
- Descriptors DEC
- ANTI-INFECTIVE AGENTS; BACTERIA; CHEMICAL REACTIONS; CHEMISTRY; CHROMATOGRAPHY; DECOMPOSITION; DRUGS; ECOSYSTEMS; HYDROGEN COMPOUNDS; LIQUID COLUMN CHROMATOGRAPHY; MICROORGANISMS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PHOTOCHEMICAL REACTIONS; RADICALS; SEPARATION PROCESSES; WATER
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.