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Simultaneous determination of three naturally occurring estrogens in environmental waters by high-performance liquid chromatography

✍ Scribed by Chengjun Wang; Chunmei Xu; Fan Chen; Xuejiao Tang


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
115 KB
Volume
34
Category
Article
ISSN
1615-9306

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✦ Synopsis


Abstract

A simple, sensitive and accurate reversed‐phase high‐performance liquid chromatographic (HPLC) method for simultaneous determination of three naturally occurring estrogenic steroids including estrone (E1), 17β‐estradiol (E2) and estriol (E3) in environmental water samples was developed. Analytes were extracted with ethyl acetate solvents and preconcentrated prior to HPLC analysis. Separations were accomplished in <20 min using a reversed‐phase C~18~ column (4.6×250 mm id, 5 μm) with a gradient elution of mobile phase containing 3.0 mM ammonium acetate/acetonitrile mixtures (flow rate, 1.0 mL/min). UV light absorption responses at 205 nm were linear over a wide concentration range from 100 000 μg/L to the detection limits of 0.96 μg/L E1, 0.64 μg/L E2 and 0.78 μg/L E3. Quantitation was carried out by the peak area method. The relative standard deviation for the analysis of three estrogens was <3.0%. This method was applied for the simultaneous determination of estrogens in environmental water samples collected in Zhejiang, China. The higher concentrations of both E2 and E3 were found in Tang River and West Lake waters, and E1 was detected in lake water only. All three estrogens were below the detection limits in rain waters.


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