Vulliet Emmanuelle, Wiest Laure, Baudot Robert, Grenier-Loustalot Marie-Florence
Service Central d'Analyse du CNRS-USR59, Chemin du Canal, B.P. 22, F-69360 Solaize, France.
J Chromatogr A. 2008 Nov 7;1210(1):84-91. doi: 10.1016/j.chroma.2008.09.034. Epub 2008 Sep 16.
Most analytical methodologies currently available for the determination of steroids in water only identify a few representative compounds (mainly estrogens). In this context, a multi-residue methodology based on liquid chromatography-tandem mass spectrometry was developed for the determination of 26 steroids including natural and synthetic estrogens, progestagens and androgens. The method described involves limited sample preparation as it includes a filtration followed by a single solid-phase extraction step using a C18 cartridge. The analytical procedure allows the determination of the target analytes in the lower ng/L range, with recoveries above 80%. The methodology was successfully applied to the analysis of steroids in several surface and ground-waters. In all the waters, estrogens, androgens and/or progestagens were determined.
目前大多数可用于测定水中类固醇的分析方法仅能识别少数几种代表性化合物(主要是雌激素)。在此背景下,开发了一种基于液相色谱 - 串联质谱的多残留方法,用于测定包括天然和合成雌激素、孕激素和雄激素在内的26种类固醇。所述方法的样品制备过程有限,包括过滤,然后使用C18柱进行单一固相萃取步骤。该分析程序能够测定低至纳克/升范围内的目标分析物,回收率高于80%。该方法已成功应用于多种地表水和地下水中类固醇的分析。在所有水样中,均检测到了雌激素、雄激素和/或孕激素。