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Solid-phase extraction using molecularly imprinted polymer for selective extraction of natural and syntetic estrogens from aqueous samples

机译:使用分子印迹聚合物固相萃取从水性样品中选择性萃取天然和合成雌激素

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摘要

A method is proposed for the clean-up and preconcentration of natural and synthetic estrogens from aqueous samples employing molecularly imprinted polymer (MIP) as selective sorbent for solid-phase extraction (SPE). The selectivity of the MIP was checked toward several selected natural and synthetic estrogens such as estrone (E1), 17β-estradiol (β-E2), 17α-estradiol (α-E2), estriol (E3), 17α-ethinylestradiol (EE2), dienestrol (DIES) and diethylstilbestrol (DES). Ultrahigh pressure liquid chromatography (UHPLC) coupled to a TSQ triple quadrupole mass spectrometry (QqQ) was used for analysis of target analytes. The chromatographic separation of the selected compounds was performed in less than 2 min under isocratic conditions. The method was applied to the analysis of estrogens in spiked river and tap water samples. High recoveries (>82%) for estrone, 17β-estradiol, 17α-estradiol, estriol and 17α-ethinylestradiol were obtained. Lower but still satisfactory recoveries (>48%) were achieved for dienestrol and diethylstilbestrol. The method was validated and found to be linear in the range 50-500 ng L-1 with correlation coefficients (R2) greater than 0.995 and repeatability relative standard deviation (RSD) below 8% in all cases. For analysis of 100-ml sample, the method detection limits (LOD) ranged from 4.5 to 9.8 ng L-1 and the limit of quantitation (LOQ) from 14.9 to 32.6 ng L-1. To demonstrate the potential of the MIP obtained, a comparison with commercially available C18 SPE was performed. Molecularly imprinted SPE showed higher recoveries than commercially available C18 SPE for most of the compounds. These results showed the suitability of the MIP-SPE method for the selective extraction of a class of structurally related compounds such as natural and synthetic estrogens.
机译:提出了一种使用分子印迹聚合物(MIP)作为固相萃取(SPE)的选择性吸附剂从水性样品中纯化和预浓缩天然和合成雌激素的方法。检查MIP对几种选定的天然和合成雌激素的选择性,例如雌酮(E1),17β-雌二醇(β-E2),17α-雌二醇(α-E2),雌三醇(E3),17α-乙炔雌二醇(EE2) ,己烯雌酚(DIES)和己烯雌酚(DES)。超高压液相色谱(UHPLC)与TSQ三重四极杆质谱(QqQ)耦合用于分析目标分析物。在等度条件下,不到2分钟即可完成所选化合物的色谱分离。该方法用于加标的河水和自来水样品中的雌激素分析。获得了雌酮,17β-雌二醇,17α-雌二醇,雌三醇和17α-炔雌醇的高回收率(> 82%)。己烯雌酚和己烯雌酚的回收率较低,但仍令人满意(> 48%)。该方法经过验证,发现在50-500 ng L-1范围内是线性的,在所有情况下相关系数(R2)均大于0.995,可重复性相对标准偏差(RSD)低于8%。对于100 ml样品的分析,方法的检测限(LOD)为4.5至9.8 ng L-1,定量限(LOQ)为14.9至32.6 ng L-1。为了证明获得的MIP的潜力,与市售C18 SPE进行了比较。对于大多数化合物,分子印迹SPE的回收率高于市售C18 SPE。这些结果表明,MIP-SPE方法适用于选择性提取一类结构相关化合物,例如天然和合成雌激素。

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