School of Chemistry, College of Science, University of Tehran, Tehran, Iran.
J Sep Sci. 2021 Oct;44(19):3626-3635. doi: 10.1002/jssc.202100495. Epub 2021 Aug 16.
Four new thymol-based ternary deep eutectic solvents were prepared and evaluated as the extractive phase in air-bubbles assisted dispersive liquid-liquid microextraction for extraction of tetracycline, doxycycline, and oxytetracycline from the water before high-performance liquid chromatography. The maximum extraction efficiencies were obtained using 400 μL of [choline chloride]:[thymol]:[nonanoic acid] in the molar ratio of 1:2:2 at pH = 5. The solvent was characterized by FTIR and NMR spectroscopy. The hydrophobicity of the deep eutectic solvent and its effect on the pH of water samples after mixing was also studied. Besides, the extraction efficiency of the ternary deep eutectic solvent was compared with that of two binary thymol-based deep eutectic solvents, including [choline chloride]:[thymol] and [thymol]:[nonanoic acid] at the same conditions. Under optimal conditions, limits of detection and quantification were 1.2-8.0 and 3.8-26.6 μg/L, respectively. The linear ranges were 18.2-500 μg/L for oxytetracycline, 26.6-500 μg/L for tetracycline, and 3.8-500 μg/L for doxycycline with the determination coefficients > 0.9912. Intra- and inter-day relative standard deviations were 1.2-3.8 and 7.7-11.2%, respectively. The developed method was applied to the analysis of tetracyclines in unspiked and spiked environmental water samples, and the obtained recoveries were 74.5-95.4% with relative standard deviations of 1.2-4.0%.
四种新的基于麝香草酚的三元深共晶溶剂被制备并评价为在空气泡辅助分散液-液微萃取中的萃取相,用于从水相中萃取四环素、强力霉素和土霉素,然后进行高效液相色谱分析。在 pH = 5 时,使用 400 μL 的 [胆碱氯化物]:[麝香草酚]:[壬酸]摩尔比为 1:2:2 的溶剂,可获得最大的萃取效率。深共晶溶剂的特征通过傅里叶变换红外光谱和核磁共振波谱进行了表征。还研究了深共晶溶剂的疏水性及其对混合后水样 pH 值的影响。此外,还在相同条件下,将三元深共晶溶剂的萃取效率与两种基于麝香草酚的二元深共晶溶剂,包括 [胆碱氯化物]:[麝香草酚]和 [麝香草酚]:[壬酸]的萃取效率进行了比较。在最佳条件下,土霉素的检测限和定量限分别为 1.2-8.0 和 3.8-26.6 μg/L,线性范围为 18.2-500 μg/L;四环素的检测限和定量限分别为 26.6-500 μg/L 和 3.8-500 μg/L;强力霉素的检测限和定量限分别为 3.8-500 μg/L 和 3.8-500 μg/L,相关系数均大于 0.9912。日内和日间相对标准偏差分别为 1.2-3.8%和 7.7-11.2%。该方法被应用于未加标和加标环境水样中四环素的分析,获得的回收率为 74.5-95.4%,相对标准偏差为 1.2-4.0%。