Department of Chemistry, Tarbiat Modares University, Tehran, Iran.
J Sep Sci. 2012 Feb;35(4):571-9. doi: 10.1002/jssc.201100869.
Electromembrane extraction followed by high-performance liquid chromatography coupled with ultraviolet detection was validated for the determination and quantification of salbutamol (SB) and terbutaline in aqueous samples. A 200-V electrical field was applied to extract the analytes from 2.5 mL sample solution with pH 3.0, through an organic phase which consisted of 80% 2-nitrophenyl octyl ether, 10% di-(2-ethylhexyl) phosphate and 10% tris-(2-ethylhexyl)phosphate as supported liquid membrane into an acidic acceptor solution with pH 1.0, located inside the lumen of a hollow fiber. To achieve the best extraction conditions, the organic membrane composition was optimized separately and other parameters, such as extraction time, applied voltage and pH in sample solution and acceptor phase were studied using experimental design. Under optimal conditions, extraction recoveries of 53 and 43% were obtained for SB and terbutaline, respectively, which corresponded to preconcentration factors of 89 for SB and 72 for terbutaline. The method offers acceptable linearity with correlation coefficient higher than 0.9947 and relative standard deviation less than 4.7%. Finally, it was applied for analysis of drugs in wastewater samples.
采用电渗析萃取结合高效液相色谱-紫外检测法,对水相样品中的沙丁胺醇(SB)和特布他林进行了测定和定量分析。在 200 V 的电场作用下,pH 值为 3.0 的 2.5 mL 样品溶液中的分析物通过有机相萃取,有机相由 80% 2-硝基苯基辛基醚、10% 二(2-乙基己基)磷酸酯和 10% 三(2-乙基己基)磷酸酯组成,进入位于中空纤维内腔的 pH 值为 1.0 的酸性接受溶液中。为了达到最佳萃取条件,分别优化了有机膜组成,同时还使用实验设计研究了萃取时间、施加电压以及样品溶液和接受相中的 pH 值等其他参数。在最佳条件下,SB 和特布他林的萃取回收率分别为 53%和 43%,对应的预浓缩因子分别为 89 和 72。该方法具有可接受的线性度,相关系数高于 0.9947,相对标准偏差小于 4.7%。最后,该方法被应用于废水样品中药物的分析。