Pharmacogenomics Laboratory, Centre Hospitalier Universitaire (CHU) de Québec - Université Laval Research Center and Faculty of Pharmacy, Laval University, Québec city, QC, Canada.
Pharmacogenomics Laboratory, Centre Hospitalier Universitaire (CHU) de Québec - Université Laval Research Center and Faculty of Pharmacy, Laval University, Québec city, QC, Canada; Canada Research Chair in Pharmacogenomics, Canada.
J Chromatogr A. 2021 Aug 2;1650:462228. doi: 10.1016/j.chroma.2021.462228. Epub 2021 May 8.
Bioactive 11-oxygenated C adrenal-derived steroids (11-oxy C) are potentially relevant in diverse endocrine and metabolic contexts. We report the development and validation of a liquid chromatography electrospray ionization tandem mass spectrometric method (LC-ESI-MS/MS) for the simultaneous quantification of seven 11-oxy C using 200 µL of plasma or serum. Sample preparation involved chemical derivatization using hydroxylamine after liquid-liquid extraction to improve specificity and sensitivity. The method allowed the quantitation of total 11-oxy C (free + sulfate and glucuronide conjugates) following enzymatic hydrolysis. This included the abundant precursor 11-hydroxyandrostenedione (11OHA4) and the most potent androgenic derivatives 11-keto-testosterone (11KT) and 11-keto-dihydrotestosterone (11KDHT), their abundant metabolites 11-hydroxyandrosterone (11OHAST) and 11-keto-androsterone (11KAST) potentially feeding back into the pool of potent androgens, in addition to 11-keto-androstenedione (11KA4) and 11-hydroxytestosterone (11OHT). Stable isotopes were used as internal standards, and calibrators and quality controls were prepared in the same matrix as the study samples. Performance was validated against the Food and Drug Administration Criteria. The method was sensitive with lower limit of quantification (LLOQ) values of 10 and 20 pg/mL for free and total 11-oxy C, respectively. The applicability was demonstrated in men and women adult donors that showed sex-differences. All steroids were quantified well above LLOQ, except 11KDHT that remained undetectable suggesting interfering endogenous molecules present in non-derivatized samples in which a peak was observed. By providing accurate and reliable quantitative data, this method will permit to evaluate how profiling of 11-oxy C will be most informative as diagnostic, prognostic and/or theranostic tools.
生物活性 11-氧代 C 肾上腺衍生类固醇(11-oxy C)在各种内分泌和代谢背景下可能具有相关性。我们报告了一种液相色谱-电喷雾串联质谱法(LC-ESI-MS/MS)的开发和验证,该方法可同时定量分析 7 种 11-oxy C,使用 200µL 血浆或血清。样品制备涉及在液液萃取后使用羟胺进行化学衍生化,以提高特异性和灵敏度。该方法允许在酶水解后定量测定总 11-oxy C(游离+硫酸盐和葡萄糖醛酸缀合物)。这包括丰富的前体 11-羟基雄烯二酮(11OHA4)和最有效的雄激素衍生物 11-酮睾酮(11KT)和 11-酮二氢睾酮(11KDHT),以及它们丰富的代谢物 11-羟基雄甾酮(11OHAST)和 11-酮雄甾酮(11KAST),这些代谢物可能反馈到强效雄激素池中,此外还有 11-酮雄烯二酮(11KA4)和 11-羟睾酮(11OHT)。稳定同位素用作内标,校准品和质控品在与研究样本相同的基质中制备。性能符合食品和药物管理局标准。该方法具有较高的灵敏度,游离和总 11-oxy C 的定量下限(LLOQ)值分别为 10 和 20 pg/mL。该方法在男性和女性成年供体中具有适用性,显示出性别差异。所有类固醇的定量值均远高于 LLOQ,除 11KDHT 外,11KDHT 仍无法检测到,表明在未经衍生化的样品中存在干扰内源性分子,在未经衍生化的样品中观察到一个峰。通过提供准确可靠的定量数据,该方法将能够评估 11-oxy C 谱分析作为诊断、预后和/或治疗工具的信息性如何。