LC-HRMS of derivatized urinary estrogens and estrogen metabolites in postmenopausal women

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Lancia N.F. Darville , Jayden K. Cline , Carrie Rozmeski , Yessica C. Martinez , Shannan Rich , Steven A. Eschrich , Kathleen M. Egan , Lusine Yaghjyan , John M. Koomen
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引用次数: 3

Abstract

In order to undertake an epidemiologic study relating levels of parent estrogens (estrone and estradiol) and estrogen metabolites (EMs) to other breast cancer risk factors, we have optimized methods for EM quantification with ultra high performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS). A two-step approach was adopted; the first step comprised method development and evaluation of the method performance. The second step consisted of applying this method to quantify estrogens in postmenopausal women and determine if the observed patterns are consistent with the existing literature and prior knowledge of estrogen metabolism. First, 1-methylimidazole-2-sulfonyl chloride (MIS) was used to derivatize endogenous estrogens and estrogen metabolites in urine from study participants. Since C18 reversed phase columns have not been able to separate all the structurally related EMs, we used a C18-pentafluorophenyl (PFP) column. The parent estrogens and EMs were baseline resolved with distinct retention times on this C18-PFP column using a 30 min gradient. This method was used to quantify the parent estrogens and 13 EMs in urine samples collected in an initial pilot study involving males as well as pre- and peri-menopausal females to assess a range of EM levels in urine samples and enable comparison to the previous literature for assay evaluation. Detection limits ranged from 1 − 20 pg/mL depending on the EM. We evaluated matrix effects and interference as well as the intra- and inter-batch reproducibility including hydrolysis, extraction, derivatization and LC-MS analysis using charcoal-stripped human urine as a matrix. Methods were then applied to the measurement of estrogens in urine samples from 169 postmenopausal women enrolled in an epidemiological study to examine relationships between breast cancer risk, the intestinal microbiome, and urinary EMs. The results from our cohort are comparable to previous reports on urinary EMs in postmenopausal women and enabled thorough evaluation of the method.

绝经后妇女衍生性尿雌激素和雌激素代谢物的LC-HRMS
为了开展母体雌激素(雌酮和雌二醇)和雌激素代谢物(EMs)水平与其他乳腺癌危险因素之间的流行病学研究,我们优化了超高效液相色谱-高分辨率质谱(UHPLC-HRMS)的EM定量方法。采取了两步办法;第一步包括方法开发和方法性能评估。第二步是应用该方法量化绝经后妇女的雌激素,并确定观察到的模式是否与现有文献和先前对雌激素代谢的认识一致。首先,1-甲基咪唑-2-磺酰氯(MIS)被用于衍生研究参与者尿液中的内源性雌激素和雌激素代谢物。由于C18反相色谱柱无法分离所有结构相关的em,我们使用了C18-五氟苯基(PFP)色谱柱。母体雌激素和EMs在C18-PFP柱上以30分钟梯度以不同的保留时间基线分离。该方法用于量化在最初的试点研究中收集的尿液样本中的母体雌激素和13种EM,该研究涉及男性以及绝经前和围绝经期女性,以评估尿液样本中的EM水平范围,并与先前的文献进行比较,以进行分析评估。检测限范围为1 - 20 pg/mL,取决于EM。我们评估了基质效应和干扰,以及批内和批间的重现性,包括水解、提取、衍生化和LC-MS分析,使用炭剥离的人尿作为基质。然后应用方法测量了169名绝经后妇女尿液样本中的雌激素,这些妇女参加了一项流行病学研究,以检查乳腺癌风险、肠道微生物群和尿液EMs之间的关系。我们队列研究的结果与先前关于绝经后妇女泌尿系统EMs的报告相比较,并对该方法进行了全面的评估。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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