Ultrasound-assisted dispersive liquid-liquid microextraction for determination of enrofloxacin in surface waters
[Display omitted] •UA-DLLME was applied for clean-up and concentration of ENRO in aqueous samples.•UA-DLLME–HPLC–FLD provides low detection limits (0.11 µg L−1) for river water.•Recovery results in river water sample ranged from 72 to 120 %.•ENRO was detected in the river water analyzed at concentra...
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Veröffentlicht in: | Microchemical journal 2021-01, Vol.160, p.105633, Article 105633 |
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•UA-DLLME was applied for clean-up and concentration of ENRO in aqueous samples.•UA-DLLME–HPLC–FLD provides low detection limits (0.11 µg L−1) for river water.•Recovery results in river water sample ranged from 72 to 120 %.•ENRO was detected in the river water analyzed at concentration of 0.20 µg L−1.
This work describes the development of an HPLC-FLD methodology for the separation of five fluoroquinolones (ciprofloxacin, enrofloxacin, sarafloxacin, norfloxacin and levofloxacin) followed by optimization of the DLLME process for the clean-up and preconcentration of enrofloxacin in samples of seawater and river water. The mobile phase used for the chromatographic separation consisted of methanol: phosphate buffer (NaHPO4 H2O 0.04 M pH 3 with H3PO4 85%), gradient eluted at a ratio of 20:80 (v:v). The mobile phase flow was maintained at 1.2 mL min−1. For the ultrasonic-assisted dispersive liquid-liquid microextraction (UA-DLLME), the following conditions were used: 8 mL of sample with pH adjusted to 8, extraction solvent: 500 μL of chloroform, dispersive solvent: 500 μL of acetonitrile; samples were vortexed and sonicated for 2 min, each. The enrichment factor (EF) was 54.7 and the recovery was 70%, achieving a limit of detection (LOD) of 0.11 µg L−1. Repeatability and intermediate reproducibility presented values of relative standard deviation (RSD) lower than 2%. Finally, the optimized method was applied to the analysis of water and enrofloxacin was detected in both water samples with a concentration of 0.20 µg L−1 in the river and 0.12 µg L−1 in the seawater. However, recovery tests performed to evaluate the water matrices' effects on the extraction performance, presented recoveries of 72 ± 6.1 for river water and 27 ± 8.3 for seawater. These results demonstrate that hereby developed method is only suitable for water samples with a low salinity content. |
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ISSN: | 0026-265X 1095-9149 |
DOI: | 10.1016/j.microc.2020.105633 |