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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Dynamic liquid-liquid-solid microextraction based on molecularly imprinted polymer filaments on-line coupling to high performance liquid chromatography for direct analysis of estrogens in complex samples
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Dynamic liquid-liquid-solid microextraction based on molecularly imprinted polymer filaments on-line coupling to high performance liquid chromatography for direct analysis of estrogens in complex samples

机译:基于分子印迹聚合物细丝的动态液-液-固微萃取在线耦合至高效液相色谱法,可直接分析复杂样品中的雌激素

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A novel sample preparation technique termed dynamic liquid-liquid-solid microextraction (DLLSME) was developed and on-line coupled to high performance liquid chromatography (HPLC) for direct extraction, desorption, and analysis of trace estrogens in complex samples. The DLLSME consists of the aqueous donor phase, the organic medium phase and the molecularly imprinted polymer filaments (MIPFs) as solid acceptor phase. The organic solvent with lesser density was directly added on top of the aqueous sample, and the dynamic extraction was performed by circulating the organic solvent through the MIPFs inserted into a PEEK tube which served as an extraction and desorption chamber. Afterwards, the extracted analytes on the MIPFs were on-line desorbed and then introduced into the HPLC for analysis. To evaluate the feasibility of the on-line system, a new DLLSME-HPLC method was developed for the analysis of five estrogens in aqueous samples by using 17β-estradiol MIPFs as the solid phase. Under the optimized conditions, the enrichment factors of 51-70, limits of detection of 0.08-0.25. μg/L and precision within 4.5-6.9% were achieved. Furthermore, the proposed method was applied to the analysis of real samples including urine, milk and skin toner, satisfactory recovery (81.9-99.8%) and reproducibility (4.1-7.9%) were obtained. Especially, 0.59. μg/L of 17β-estradiol was determined in female urine sample. The DLLSME offers an attractive alternative for direct analysis of trace analytes in aqueous samples and could potentially be extended to other adsorptive materials.
机译:开发了一种称为动态液-液-固微萃取(DLLSME)的新型样品制备技术,并与高效液相色谱(HPLC)在线耦合,用于直接萃取,解吸和分析复杂样品中的痕量雌激素。 DLLSME由水供体相,有机介质相和分子印迹聚合物长丝(MIPF)组成,后者为固体受体相。将密度较小的有机溶剂直接添加到含水样品的顶部,通过使有机溶剂循环通过插入到用作萃取和解吸室的PEEK管中的MIPF,来进行动态萃取。然后,将MIPF上提取的分析物在线解吸,然后引入HPLC中进行分析。为了评估在线系统的可行性,通过使用17β-雌二醇MIPF作为固相,开发了一种新的DLLSME-HPLC方法来分析水性样品中的5种雌激素。在优化条件下,富集因子为51-70,检出限为0.08-0.25。微克/升,精度在4.5-6.9%之间。此外,该方法用于实际样品的分析,包括尿液,牛奶和皮肤上的碳粉,回收率令人满意(81.9-99.8%),重现性良好(4.1-7.9%)。特别是0.59。在女性尿液样品中测定了17 g-雌二醇的微克/升。 DLLSME为直接分析水性样品中的痕量分析物提供了一种有吸引力的替代方法,并且可能会扩展到其他吸附材料。

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