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Improved dispersive liquid–liquid microextraction based on the solidification of floating organic droplet method with a binary mixed solvent applied for determination of nicotine and cotinine in urine

机译:改进的基于分散有机液滴固化方法的分散液-液微萃取,采用二元混合溶剂测定尿液中的尼古丁和可替宁

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A fast, simple and environmentally friendly method to determine nicotine and cotinine in urine has been developed using dispersive liquida€“liquid microextraction based on solidification of floating organic droplet (DLLME-SFO) with a binary mixed extractant as the pretreatment method and high performance liquid chromatography with an ultraviolet detector (HPLC-UVD) as the analysis system. The nicotine and cotinine in urine samples were extracted using the binary mixed solvent of undecanol and CHCl3 (v/v = 1:1) during the DLLME-SFO procedure. The employment of the mixed solvent had significantly improved the extraction efficiency of cotinine. Several crucial experiment parameters were evaluated, including the type and volume of extract solvent, type of dispersive solvent, pH of the aqueous phase, concentration of sodium chloride in the urine samples and extraction time. Under the optimal conditions, good linearity was observed in the range of 0.01a€“5.00 ??g mLa?’1 for nicotine and cotinine with correlation coefficients of 0.9993 and 0.9996 respectively, and the method detection limit (MLD) was 0.002 ??g mLa?’1 for both analytes. The proposed method was applied to urine sample analysis and the spiked recoveries of nicotine and cotinine were in the range of 78.0a€“105.0% and 72.0a€“86.7% respectively, with the relative standard deviations (RSDs) in the range of 6.02a€“7.28% and 2.94a€“8.43% respectively.
机译:已经开发了一种快速,简单且环境友好的测定尿液中尼古丁和可替宁的方法,该方法使用分散液和液体微萃取,该液体微萃取基于浮动有机液滴(DLLME-SFO)的固化,采用二元混合萃取剂作为预处理方法和高性能液体。用紫外检测器(HPLC-UVD)作为分析系统进行色谱分离。在DLLME-SFO程序中,使用十一烷醇和CHCl3(v / v = 1:1)的二元混合溶剂提取尿液样本中的尼古丁和可替宁。混合溶剂的使用显着提高了可替宁的提取效率。评估了几个关键的实验参数,包括提取溶剂的类型和体积,分散溶剂的类型,水相的pH值,尿液样品中氯化钠的浓度和提取时间。在最佳条件下,烟碱和可替宁在0.01a?5.00?g?mLa?'1范围内观察到良好的线性,相关系数分别为0.9993和0.9996,方法检出限(MLD)为0.002? g mLa?'1表示两种分析物。将该方法应用于尿液样品分析,尼古丁和可替宁的加标回收率分别在78.0a“ 105.0%”和72.0a“ 86.7%之间,相对标准偏差(RSDs)在6.02范围分别为“ 7.28%”和“ 2.94”“ 8.43%”。

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