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基于液相色谱-串联质谱法调查人尿液中的内源性皮质类固醇谱。

Investigation of endogenous corticosteroids profiles in human urine based on liquid chromatography tandem mass spectrometry.

机构信息

Bioanalysis Research Group, IMIM, Hospital del Mar Medical Research Institute, Doctor Aiguader 88, 08003 Barcelona, Spain; Department of Experimental and Health Sciencies, Universitat Pompeu Fabra, Doctor Aiguader 88, 08003 Barcelona, Spain.

Bioanalysis Research Group, IMIM, Hospital del Mar Medical Research Institute, Doctor Aiguader 88, 08003 Barcelona, Spain.

出版信息

Anal Chim Acta. 2014 Feb 17;812:92-104. doi: 10.1016/j.aca.2013.12.030. Epub 2014 Jan 3.

Abstract

The accurate and precise measurement of endogenous corticosteroids in urine is a powerful tool to understand the biochemical state in several diseases. In this study, a rapid, accurate, and sensitive method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the quantification of 67 endogenous gluco- and mineralo-corticosteroids and progestins has been developed and validated. Sample preparation, chromatographic separation, and mass spectrometric detection were optimized. Urine samples (0.5 mL) were hydrolyzed with β-glucuronidase and the released analytes were extracted by liquid-liquid extraction. The chromatographic separation was performed in 20 min after redisolution of the extract. MS behavior of endogenous corticosteroids was evaluated in order to select the most specific precursor ion (M+H, M+NH4, or M+H-nH2O) for the detection. MS/MS determination was performed under selected reaction monitoring mode using electrospray ionization in positive mode. The method was shown to be linear (r>0.99) in the range of endogenous concentrations for all studied metabolites. Limits of detection (LOD) below 1 ng mL(-1) were typically obtained for analytes with a 3-oxo-4-ene structure whereas LODs below 15 ng mL(-1) were common for the rest of analytes. Recoveries were higher than 80% and intra-assay precisions below 20%, evaluated at three concentration levels, were found for most steroids. No significant or moderate matrix effect, ranging from 54 to 155%, was observed for most of the analytes. The applicability of the method was confirmed by analyzing 24h urine samples collected from twenty healthy volunteers and comparing the results with previously established normal ranges. The wide coverage of corticosteroid metabolism, together with short analysis time, low sample volume, simple sample preparation, and satisfactory quantitative results make this method useful for clinical purposes.

摘要

尿液中内源性皮质甾类激素的准确和精确测量是了解几种疾病生化状态的有力工具。在这项研究中,建立并验证了一种基于液相色谱-串联质谱(LC-MS/MS)的快速、准确和灵敏的方法,用于定量分析 67 种内源性糖质和矿物皮质甾类激素和孕激素。优化了样品制备、色谱分离和质谱检测。用β-葡萄糖醛酸酶水解尿液样品(0.5 mL),并用液液萃取提取释放的分析物。在提取物重新溶解后 20 分钟内完成色谱分离。评估了内源性皮质甾类激素的 MS 行为,以选择用于检测的最特异的前体离子(M+HM+NH4M+H-nH2O)。采用正电喷雾电离,在选择反应监测模式下进行 MS/MS 测定。该方法对于所有研究代谢物,在内源性浓度范围内呈线性(r>0.99)。具有 3-酮-4-烯结构的分析物通常可获得低于 1ng/mL 的检测限(LOD),而其余分析物的 LOD 通常低于 15ng/mL。在三个浓度水平下,大多数类固醇的回收率高于 80%,日内精密度低于 20%。对于大多数分析物,观察到的基质效应无显著或中等,范围为 54%至 155%。通过分析 24 小时尿液样本,该方法的适用性得到了验证,这些样本是从 20 名健康志愿者中收集的,并将结果与之前建立的正常范围进行了比较。该方法广泛涵盖皮质甾类代谢物,分析时间短,样品体积小,样品制备简单,定量结果令人满意,因此可用于临床目的。

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