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首页> 外文期刊>Analytica chimica acta >Nano polypyrrole-coated magnetic solid phase extraction followed by dispersive liquid phase microextraction for trace determination of megestrol acetate and levonorgestrel
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Nano polypyrrole-coated magnetic solid phase extraction followed by dispersive liquid phase microextraction for trace determination of megestrol acetate and levonorgestrel

机译:纳米聚吡咯涂层磁性固相萃取,然后用分散液相微萃取法测定乙酸孕甾酮和左炔诺孕酮的含量

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摘要

The aim of the present work is combination of the advantages of magnetic solid phase extraction (MSPE) and dispersive liquid phase microextraction (DLLME) followed by filtration-based phase separation. A new pretreatment method was developed for trace determination of megestrol acetate and levonorgestrel by liquid chromatography/ultraviolet detection in biological and wastewater samples. After magnetic solid phase extraction, the eluent of MSPE was used as the disperser solvent for DLLME. Emulsion resulted from DLLME procedure was passed through the in-line filter for phase separation. Finally the retained analytes in the filter was washed with mobile phase of liquid chromatography and transferred to the column for separation. This approach offers the preconcentration factors of 3680 and 3750 for megestrol acetate and levonorgestrel, respectively. This guarantees determination of the organic compounds at trace levels. The important parameters influencing the extraction efficiency were studied and optimized. Under the optimal extraction conditions, a linear range of 0.05-50 ng mL(-1) (R-2 > 0.998) and limit of detection of 0.03 ng mL(-1) were obtained for megestrol acetate and levonorgestrel. Under optimal conditions, the method was successfully applied for determination of target analytes in urine and wastewater samples and satisfactory results were obtained ( RSDs < 6.8%). (C) 2015 Elsevier B.V. All rights reserved.
机译:本工作的目的是结合磁性固相萃取(MSPE)和分散液相微萃取(DLLME)的优势,然后进行基于过滤的相分离。开发了一种新的预处理方法,用于通过液相色谱/紫外检测生物和废水样品中的乙酸甲孕酮和左炔诺孕酮。磁性固相萃取后,将MSPE的洗脱液用作DLLME的分散剂。 DLLME程序产生的乳液通过在线过滤器进行相分离。最后,用液相色谱的流动相洗涤过滤器中保留的分析物,并转移到色谱柱中进行分离。该方法分别为醋酸孕甾酮和左炔诺孕酮提供了3680和3750的预浓缩系数。这保证了痕量水平上有机化合物的测定。研究和优化了影响萃取效率的重要参数。在最佳提取条件下,乙酸甲孕酮和左炔诺孕酮的线性范围为0.05-50 ng mL(-1)(R-2> 0.998),检出限为0.03 ng mL(-1)。在最佳条件下,该方法已成功应用于尿液和废水样品中目标分析物的测定,并获得了满意的结果(相对标准偏差<6.8%)。 (C)2015 Elsevier B.V.保留所有权利。

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