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Multivariate calibration-assisted high-performance liquid chromatography with dual UV and fluorimetric detection for the analysis of natural and synthetic sex hormones in environmental waters and sediments

机译:多元校准辅助高效液相色谱仪,具有紫外和荧光双重检测功能,可分析环境水体和沉积物中的天然和合成性激素

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摘要

A green method is reported based on non-sophisticated instrumental for the quantification of seven natural and synthetic estrogens, three progestagens and one androgen in the presence of real interferences. The method takes advantage of: (1) chromatography, allowing total or partial resolution of a large number of compounds, (2) dual detection, permitting selection of the most appropriate signal for each analyte and, (3) second-order calibration, enabling mathematical resolution of incompletely resolved chromatographic bands and analyte determination in the presence of interferents. Consumption of organic solvents for cleaning, extraction and separation are markedly decreased because of the coupling with MCR-ALS (multivariate curve resolution/alternating least-squares) which allows the successful resolution in the presence of other co-eluting matrix constituents. Rigorous IUPAC detection limits were obtained: 6-24 ng L-1 in water, and 0.1-0.9 ng g(-1) in sediments. Relative prediction errors were 2-10% (water) and 1-8% (sediments). (C) 2015 Elsevier Ltd. All rights reserved.
机译:报道了一种基于非精密仪器的绿色方法,可在存在实际干扰的情况下对7种天然和合成雌激素,3种孕激素和1种雄激素进行定量。该方法具有以下优势:(1)色谱法,可对大量化合物进行全部或部分拆分;(2)双重检测,可为每种分析物选择最合适的信号;(3)二级校准,可实现在存在干扰物的情况下,未完全解析的色谱带的数学分辨率和分析物的测定。由于与MCR-ALS的耦合(多变量曲线分辨率/最小二乘法),在清洁,萃取和分离过程中有机溶剂的消耗显着降低,从而可以在存在其他共洗脱基质成分的情况下成功实现分离。获得了严格的IUPAC检测极限:水中6-24 ng L-1,沉积物中0.1-0.9 ng g(-1)。相对预测误差为2-10%(水)和1-8%(沉积物)。 (C)2015 Elsevier Ltd.保留所有权利。

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