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Development of a solid-phase extraction—enzyme-linked immunosorbent assay method for the determination of estrone in water
Estrone has been identified as a potential endocrine-disrupting chemical (EDC). To facilitate its analysis, a highly selective and sensitive enzyme-linked immunosorbent assay (ELISA) method with a simple solid-phase extraction (SPE) for analysis of estrone in aquatic environments has been developed....
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Published in: | Analytica chimica acta 2004-02, Vol.503 (2), p.171-177 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Estrone has been identified as a potential endocrine-disrupting chemical (EDC). To facilitate its analysis, a highly selective and sensitive enzyme-linked immunosorbent assay (ELISA) method with a simple solid-phase extraction (SPE) for analysis of estrone in aquatic environments has been developed. The specific polyclonal antibody was produced against a conjugate of estrone-3-hemisuccinate and keyhole limpet hemocyanin (KLH). The obtained ELISA showed specific recognition of estrone, without cross-reactions for three other major estrogenic compounds (17β-estradiol, estriol, and 17α-ethynylestradiol) commonly found in water. The ELISA had a limit of detection of 0.14
μg/l estrone in water. Combining a SPE method to extract and pre-concentrate estrone from water samples and ELISA to specifically quantify estrone content, the SPE-ELISA can detect estrone down to 1.25
ng/l level in water. Good recovery with spiked river water was obtained with this SPE-ELISA method. The developed SPE-ELISA system was applied to analyze the real influent and effluent samples of sewage treatment plant in Penrith (Australia) and the results correlated well with those obtained using GC and HPLC methods. The developed SPE-ELISA method is capable of being applied for the specific detection and routine monitoring of estrone in environmental water samples. |
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ISSN: | 0003-2670 1873-4324 |
DOI: | 10.1016/j.aca.2003.10.026 |