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An ultrasound-assisted ionic liquid (IL) salting-out microextraction system was developed and applied for the extraction of quinolone antibiotics from urine. A precipitate was formed from the salt and IL, and it acted as the sorbent for the analytes. The precipitate containing the analyte was separated by filtration, redissolved, and the solution then was evaporated. The resulting extract was redissolved for high-performance liquid chromatographic analysis. Several parameters, including type and volume of IL, the type and amount of salts, sample pH, temperature and extraction time were optimized. Under the optimal experimental conditions, the limits of detection for fleroxacin and ciprofloxacin were 3.12 and 4.97 μg L−1, respectively. When the present method was applied to real urine sample analysis, the analyte recoveries ranged from 82.3 to 106.8%. This ultrasound-assisted IL salting-out microextraction system had the characteristics of high recoveries, shorter separation time and easy-to-perform collection procedure, which yielded the method to have potential for wide application. [ABSTRACT FROM AUTHOR]

Salting-out homogenous extraction followed by ionic liquid/ionic liquid dispersive liquid-liquid micro-extraction system was developed and applied to the extraction of sulfonamides in blood. High-performance liquid chromatography was applied to the determination of the analytes. The blood sample was centrifuged to obtain the serum. After the proteins in the serum were removed in the presence of acetonitrile, ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate, dipotassium hydrogen phosphate, ionic liquid 1-Hexyl-3-methylimidazolium hexafluorophosphate were added into the resulting solution. After the resulting mixture was ultrasonically shaken and centrifuged, the precipitate was separated. The acetonitrile was added in the precipitate and the analytes were extracted into the acetonitrile phase. The parameters affecting the extraction efficiency, such as volume of ionic liquid, amount of dipotassium hydrogen phosphate, volume of dispersant, extraction time and temperature were investigated. The limits of detection of sulfamethizole (STZ), sulfachlorpyridazine (SCP), sulfamethoxazole (SMX) and Sulfisoxazole (SSZ) were 4.78, 3.99, 5.21 and 3.77 μg L −1 , respectively. When the present method was applied to the analysis of real blood samples, the recoveries of analytes ranged from 90.0% to 113.0% and relative standard deviations were lower than 7.2%. [ABSTRACT FROM AUTHOR]

Ionic liquid/anionic surfactant aqueous two-phase system was developed and applied for the extraction of Sudan I–IV. High-performance liquid chromatography was applied to the determination of the analytes. The aqueous two-phase system (ATPS) was formed in the present of C 4 [MIM]BF 4 , sodium dodecyl benzene sulphonate and (NH 4 ) 2 SO 4 . The parameters affecting the extraction efficiency, such as volume of ionic liquid, amount of sodium dodecyl benzene sulphonate, ionic strength, pH value of system, extraction time and temperature were investigated. The limits of detection for Sudan I, II, III and IV were 5.45, 4.66, 3.68, 4.20 μg kg −1 , respectively. When the present method was applied to the analysis of candy samples, the recoveries of the analytes ranged from 82.3% to 112.1% and relative standard deviations were lower than 7.41%. [ABSTRACT FROM AUTHOR]

Ionic liquid/anionic surfactant aqueous two-phase system was developed and applied for the extraction of sulfonamides in blood. High-performance liquid chromatography was applied to the determination of the analytes. The blood sample was centrifuged and added to sodium dodecyl sulfate (SDS), ionic liquid 1-Hexyl-3-MethylImidazolium Chloride([C 6 MIM] Cl), K 2 HPO 4 . After the resulting mixture was ultrasonically shaken and centrifuged, the aqueous two phase system was formed and analytes were extracted into the upper phase. The parameters affecting the extraction efficiency, such as volume of ionic liquid, amount of sodium dodecyl sulfate, ionic strength, pH value of system, extraction time and temperature were investigated. The limits of detection of Sulfamethyldiazine (SMZ), Sulfamethizole (STZ), sulfachlorpyridazine (SCP), sulfamethoxazole (SMX) and Sulfisoxazole (SSZ) were 3.29, 4.13, 3.74, 2.45 and 3.60 μg L − 1 , respectively. When the present method was applied to the analysis of real blood samples, the recoveries of analytes ranged from 85.5 to 110.9% and relative standard deviations were lower than 6.9%. [ABSTRACT FROM AUTHOR]

Abstract: An ionic liquid-anionic surfactant based aqueous two-phase extraction was developed and applied for the extraction of tetracycline, oxytetracycline and chloramphenicol in honey. The honey sample was mixed with Na2EDTA aqueous solution. The sodium dodecyl sulfate, ionic liquid 1-octyl-3-methylimidazolium bromide and sodium chloride were added in the mixture. After the resulting mixture was ultrasonically shaken and centrifuged, the aqueous two phase system was formed and analytes were extracted into the upper phase. The parameters affecting the extraction efficiency, such as the volume of ionic liquid, the category and amount of salts, sample pH value, extraction time and temperature were investigated. The limits of detection of tetracycline, oxytetracycline and chloramphenicol were 5.8, 8.2 and 4.2μgkg−1, respectively. When the present method was applied to the analysis of real honey samples, the recoveries of analytes ranged from 85.5 to 110.9% and relative standard deviations were lower than 6.9%. [Copyright &y& Elsevier]

Abstract: Ultrasound-assisted ionic liquid/ionic liquid-dispersive liquid–liquid microextraction (UA-IL/IL-DLLME) high-performance liquid chromatography was developed and applied to the extraction, separation and determination of sulfonamides in infant formula milk powder samples. The hydrophobic IL and hydrophilic IL were used as extraction solvent and dispersion solvent, respectively. The extraction procedure was induced by the formation of cloudy solution, which was composed of fine drops of [C6MIM][PF6] dispersed entirely into sample solution with help of [C4MIM][BF4]. The purification of sample and concentration of target analytes were performed simultaneously. The introduction of ion-pairing agent (NH4PF6) was beneficial to the improvement of recoveries for IL phase and analytes. The experimental parameters of the UA-IL/IL-DLLME, including concentration of [C6MIM][PF6] and [C4MIM][BF4] in sample solution, ultrasound extraction time, pH value of sample solution and amount of ion-pairing agent (NH4PF6), were evaluated. The limits of detection for sulfamerazine, sulfamethizole, sulfachlorpyridazine, sulfamonomethoxine, sulfmethoxazole and sulfisoxazole were 2.94, 9.26, 16.7, 5.28, 3.35 and 6.66μgkg−1, respectively. When the present method was applied to the analysis of infant formula milk powder samples, the recoveries of the analytes ranged from 90.4% to 114.8% and relative standard deviations were lower than 7.5%. The proposed method was compared with the ionic liquid-homogeneous liquid–liquid microextraction, ionic liquid-ultrasound-assisted emulsification–microextraction and ionic liquid-temperature-controlled-DLLME. The results indicated that the proposed method is effective for the extraction of the sulfonamides in milk powder samples. [Copyright &y& Elsevier]