Broad range analysis of endocrine disruptors and pharmaceuticals using gas chromatography and liquid chromatography tandem mass spectrometry
被引:211
作者:
Trenholm, Rebecca A.
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So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USASo Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Trenholm, Rebecca A.
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Vanderford, Brett J.
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So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USASo Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Vanderford, Brett J.
[1
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Holady, Janie C.
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So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USASo Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Holady, Janie C.
[1
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Rexing, David J.
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So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USASo Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Rexing, David J.
[1
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Snyder, Shane A.
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So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USASo Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Snyder, Shane A.
[1
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机构:
[1] So Nevada Water Author, Water Qual Res & Dev Dept, Henderson, NV 89015 USA
Endocrine disrupting compounds (EDCs) and pharmaceuticals and personal care products (PPCPs) have been globally detected in impacted natural waters. The detection of trace quantities of EDCs and PPCPs in the environment is of great concern since some of these compounds have known physiological responses at low concentrations. EDCs can have a wide range of polarities, acidic and basic moieties, and exist in trace quantities, which often requires numerous complex extractions, large sample collection volumes, and multiple instrumental analyses. A comprehensive method has been developed allowing for the analysis of 58 potential EDCs in various water matrices using a single solid-phase extraction (SPE) of a 1 L sample with subsequent analyses using both gas chromatography and liquid chromatography, each coupled with tandem mass spectrometry (GC-MS/MS and LC-MS/MS). Instrument detection limits ranged between 0.12-7.5 pg with corresponding method reporting limits of 1-10 ng l(-1) in water. Recoveries for most compounds were between 50%, and 112% with good reproducibility (RSD 6-22%). (c) 2006 Elsevier Ltd. All rights reserved.