首页> 外文期刊>Iranian Journal of Pharmaceutical Research >Determination of Two Antiepileptic Drugs in Urine by Homogenous Liquid-Liquid Extraction Performed in A Narrow Tube Combined With Dispersive Liquid-liquid Microextraction Followed by Gas Chromatography-flame Ionization Detection
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Determination of Two Antiepileptic Drugs in Urine by Homogenous Liquid-Liquid Extraction Performed in A Narrow Tube Combined With Dispersive Liquid-liquid Microextraction Followed by Gas Chromatography-flame Ionization Detection

机译:窄管均匀液萃取-分散液-液微萃取-气相色谱-火焰电离检测联用测定尿中两种抗癫痫药

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A simple and efficient homogenous liquid-liquid extraction method performed in a narrow tube combined with dispersive liquid-liquid microextraction method has been presented for the simultaneous determination of two antiepileptic drugs in urine followed by gas chromatography with flame ionization detection. In this method, a mixture of acetonitrile and urine sample (homogenous solution) is loaded into a column partially filled with solid sodium chloride. By passing the homogenous solution through the salt layer, acetonitrile is separated from the aqueous solution as the fine droplets and collected on top of the column as a separated phase. The obtained organic phase is removed and mixed with an extraction solvent, and then the resulting mixture is rapidly injected into an alkaline solution. Various experimental parameters affecting performance of the proposed method such as type and volume of extraction solvent, pH, and flow rate in homogenous liquid-liquid extraction step, and type and volume of extraction solvent and ionic strength in dispersive liquid-liquid microextraction step were investigated. The relative standard deviation of the proposed method was 8% (n = 6, C = 1 ?μg L-1 of each analyte). The limits of detection for phenobarbital and carbamazepine were 0.017 and 0.010 ?μg L-1 and the limits of quantification were 0.056 and 0.033 ?μg mL-1, respectively.
机译:提出了一种在窄管中进行的简单有效的均质液-液萃取方法与分散液-液微萃取方法相结合的方法,用于同时测定尿液中的两种抗癫痫药,然后进行气相色谱-火焰电离检测。在这种方法中,将乙腈和尿液样品(均相溶液)的混合物装入部分装有固体氯化钠的色谱柱中。通过使均匀溶液通过盐层,将乙腈作为细小液滴从水溶液中分离出来,并作为分离相收集在塔顶。除去获得的有机相,并与萃取溶剂混合,然后将所得混合物快速注入碱性溶液中。研究了影响该方法性能的各种实验参数,如均相液-液萃取步骤中萃取溶剂的类型和体积,pH值和流速,以及分散液-液微萃取步骤中萃取溶剂的类型和体积以及离子强度。该方法的相对标准偏差<8%(每种分析物的n = 6,C = 1μgL-1)。苯巴比妥和卡马西平的检出限分别为0.017和0.010μgL-1,定量限为0.056和0.033μgmL-1。

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