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Analysis of estrogens in river water and effluents using solid-phase extraction and gas chromatography–negative chemical ionisation mass spectrometry of the pentafluorobenzoyl derivatives

2001; Elsevier BV; Volume: 923; Issue: 1-2 Linguagem: Inglês

10.1016/s0021-9673(01)00955-4

1873-3778

Xiao-Yao Xiao, David V. McCalley, J. McEvoy,

Effects and risks of endocrine disrupting chemicals

A procedure was developed for the analysis of estrogens in environmental water and effluents. Samples were extracted by passing through polymer-impregnated solid-phase extraction discs or C18 cartridges, followed by gas chromatography–negative chemical ionisation mass spectrometry of the pentafluorobenzoyl derivatives. The derivatives were stable and gave diagnostic negative molecular ions as the base peak for each of the major estrogens studied. The absolute recovery of estrogens spiked into clean groundwater using the disc procedure was 84–116% at the 10 ng l−1 level (calculation not based on use of internal standards). Using doubly deuterated estradiol as internal standard added prior to extraction, the % relative standard deviation of estrogen extraction and analysis in spiked groundwater at the 10 ng l−1 level was 2.6–9.8%. Detection limits were 0.2 ng l−1 or below for the major estrogens, based on a 2.5 litre sample. The most abundant estrogen was estrone, with concentrations over the range 6.4–29 ng l−1 in effluents, and 0.2 to 17 ng l−1 in water from the River Thames.