Service Central d'Analyse du CNRS-USR59, Chemin du Canal, 69360 Solaize, France.
Anal Bioanal Chem. 2010 Jul;397(6):2295-302. doi: 10.1007/s00216-010-3787-4. Epub 2010 May 7.
The aim of this study was to develop an efficient, sensitive and reliable analytical method for the determination of traces of steroid hormones (including oestrogen, androgens and progestagens) and corticosteroids in soil. A method of sample preparation involving pressurized liquid extraction (PLE) and solid-phase extraction (SPE) was developed for the determination of six steroids and five corticosteroids in soils, followed by analysis by liquid chromatography-tandem mass spectrometry. The conditions employed for PLE involved acetone/methanol (50:50) as the extracting solvent, a temperature of 80 degrees C, two cycles and a static time of 5 min. The extraction was followed by a SPE clean-up based on a polymeric phase. With use of protocol, a residual matrix effect was, however, highlighted. The limit of detection in soil was 0.08-0.89 ng/g for steroids and 0.09-2.84 ng/g for corticosteroids.
本研究旨在开发一种高效、灵敏、可靠的分析方法,用于测定土壤中痕量的甾体激素(包括雌激素、雄激素和孕激素)和皮质类固醇。采用加压液体萃取(PLE)和固相萃取(SPE)相结合的样品制备方法,对土壤中的六种甾体激素和五种皮质类固醇进行了测定,然后采用液相色谱-串联质谱法进行分析。PLE 的条件为丙酮/甲醇(50:50)作为提取溶剂,温度 80℃,循环两次,静态时间 5min。萃取后采用聚合物相进行 SPE 净化。然而,使用该方案时,残留基质效应明显。甾体激素在土壤中的检测限为 0.08-0.89ng/g,皮质类固醇为 0.09-2.84ng/g。