University of Applied Sciences and Arts Northwestern Switzerland, School of Life Sciences, Gründenstrasse 40, CH-4132 Muttenz, Switzerland.
University of Applied Sciences and Arts Northwestern Switzerland, School of Life Sciences, Gründenstrasse 40, CH-4132 Muttenz, Switzerland; Swiss Federal Institute of Technology Zürich (ETH Zürich), Department of Environmental Systems Science, Institute of Biogeochemistry and Pollution Dynamics, CH-8092 Zürich, Switzerland.
Sci Total Environ. 2018 Jan 1;610-611:1164-1172. doi: 10.1016/j.scitotenv.2017.08.114. Epub 2017 Aug 30.
A highly sensitive and robust method was developed for routine analysis of two progestin metabolites, 17α-hydroxypregnanolone (17OH-Δ5P) and pregnanediol (PD), and 31 other natural and synthetic steroids and related metabolites (estrogens, androgens, corticosteroids, progestins) in river water, as well as influents and effluents of municipal wastewater treatment plants (WWTP) using HPLC-MS/MS combined with solid-phase extraction. For the various matrixes considered, the optimized method showed satisfactory performance with recoveries of 70-120% for most of target steroids. The method detection limits (MDLs) ranged from 0.01 to 3ng/L for river water, 0.02 to 10ng/L for WWTP effluents, and 0.1 to 40ng/L for influents with good linearity and reproducibility. The developed method was successfully applied for the analysis of steroids in rivers and WWTP influent and effluents. WWTP influents concentrations of 17OH-Δ5P and PD were 51-256ng/L and up to 400ng/L, respectively, along with androstenedione (concentration range: 38-220ng/L), testosterone (11-26ng/L), estrone (2.3-37ng/L), 17β-estradiol (N.D.-8.7ng/L), 17α-hydroxyprogesterone (N.D.-66ng/L), medroxyprogesterone acetate (N.D.-5.3ng/L), and progesterone (2.0-22ng/L), while only androstenedione (ADD), estrone (E1), and estriol (E3) were detected in effluent with concentrations ranging up to 1.7ng/L, 0.90ng/L and 0.8ng/L, respectively. In river water samples, only ADD and E1 were detected with concentrations up to 1.0ng/L and 0.91ng/L. Our procedure represents the first method for analyzing 17OH-Δ5P and PD in environmental samples along with a large series of steroids.
建立了一种灵敏、稳健的方法,用于高效液相色谱-串联质谱法(HPLC-MS/MS)结合固相萃取,分析河流水中两种孕激素代谢物(17α-羟孕烯醇酮(17OH-Δ5P)和孕烷二醇(PD))以及 31 种天然和合成甾体及相关代谢物(雌激素、雄激素、皮质类固醇、孕激素)的常规分析,以及城市污水处理厂(WWTP)的进水和出水。对于所考虑的各种基质,该优化方法对于大多数目标甾体的回收率为 70-120%,表现出令人满意的性能。方法检测限(MDL)范围为河流水中 0.01-3ng/L,WWTP 出水中 0.02-10ng/L,进水为 0.1-40ng/L,具有良好的线性和重现性。所建立的方法成功地应用于河流和 WWTP 进水和出水的甾体分析。WWTP 进水 17OH-Δ5P 和 PD 的浓度分别为 51-256ng/L 和高达 400ng/L,同时还有雄烯二酮(浓度范围:38-220ng/L)、睾酮(11-26ng/L)、雌酮(2.3-37ng/L)、17β-雌二醇(未检出-8.7ng/L)、17α-羟孕酮(未检出-66ng/L)、醋酸甲羟孕酮(未检出-5.3ng/L)和孕酮(2.0-22ng/L),而只有雄烯二酮(ADD)、雌酮(E1)和雌三醇(E3)在出水中被检出,浓度分别高达 1.7ng/L、0.90ng/L 和 0.8ng/L。在河水水样中,仅检测到 ADD 和 E1,浓度高达 1.0ng/L 和 0.91ng/L。我们的方法代表了第一个分析环境样品中 17OH-Δ5P 和 PD 以及大量甾体的方法。