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Two-phase elect rod riven membrane extraction combined with liquid chromatography for the determination of tricyclic antidepressants in aqueous matricest

机译:两相电杆裂膜分离-液相色谱法测定水性基质中的三环类抗抑郁药

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摘要

A two-phase low-voltage electrodriven membrane extraction (EME) method combined with high performance liquid chromatography (HPLC) was developed for the determination of tricyclic antidepressants (TCAs) in aqueous matrices. Three TCAs, namely imipramine (IMI), amitriptyline (AMI) and chlorpromazine (CHLO) were used as target analytes. The drugs were extracted from aqueous sample solutions through a porous polypropylene membrane filter impregnated with 2-nitrophenyl octyl ether (NPOE) that served as a supported liquid membrane (SLM), and into an acceptor phase with a potential difference of 10 V applied over the SLM. EME parameters such as the type of organic solvent, the pH of sample solution, the extraction voltage, extraction time and stirring rate were evaluated and optimized. Optimal extractions were accomplished using NPOE as the organic solvent, a sample solution of pH 6, an extraction time of 10 min, and 10 V as the driving force with the whole assembly agitated at 1200 rpm. Under the optimized extraction conditions, the method demonstrated good linearity with coefficients of determination, r2 a 0.9987 in the concentration range of 0.5-1000 μg L~(-1) for water, and 1.0-1000 μg L~(-1) for urine and good limits of detection in the range of 0.05-0.08 μg L~(-1) and 0.1-0.3 jig L~(-1) in water and urine samples, respectively. The method showed high enrichment factors in the range of 91-128 and high relative recoveries in the range of 98.4-103.1% and 86.7-107.4%, for water and urine samples, respectively with RSDs of <9.0% (n = 3). This method was successfully applied to the determination of the drugs in water and human urine samples. The proposed method offered good features such as simplicity, easy handling, fast extraction time, low voltage and minimum organic solvent consumption which meet the green chemistry concept.
机译:建立了两相低压电驱动膜萃取(EME)与高效液相色谱(HPLC)相结合的方法,用于测定水性基质中的三环类抗抑郁药(TCA)。三种TCA,即丙咪嗪(IMI),阿米替林(AMI)和氯丙嗪(CHLO)被用作目标分析物。药物从水溶液样品中提取出来,通过多孔聚丙烯膜过滤器浸渍了2-硝基苯基辛基醚(NPOE),该膜用作支撑液膜(SLM),并进入一个受体相,该相上的电位差为10V。 SLM。评估并优化了EME参数,例如有机溶剂的类型,样品溶液的pH值,萃取电压,萃取时间和搅拌速率。使用NPOE作为有机溶剂,pH值为6的样品溶液,10分钟的提取时间以及10 V作为驱动力(以1200 rpm搅拌整个组件)完成了最佳提取。在最佳提取条件下,该方法具有良好的线性和测定系数,在0.5-1000μgL〜(-1)的浓度范围内,对于尿液,在1.0-1000μgL〜(-1)的浓度范围内,r2 = 0.9987。在水和尿液样品中的检出限分别为0.05-0.08μgL〜(-1)和0.1-0.3 jig L〜(-1)。该方法显示水和尿液样品的富集系数在91-128范围内,相对回收率分别在98.4-103.1%和86.7-107.4%范围内,相对标准偏差<9.0%(n = 3)。该方法已成功应用于水和人尿样品中药物的测定。所提出的方法具有良好的功能,如简单,易于操作,提取时间短,电压低和有机溶剂消耗最少,符合绿色化学概念。

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