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A liquid chromatography-tandem mass spectrometry assay for the profiling of classical and 11-oxygenated androgens in saliva

机译:液相色谱 - 串联质谱法测定唾液中经典和11-氧化雄激素的分析

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Background Classical and 11-oxygenated androgens both contribute to the androgen pool. Regular monitoring of the androgen status is required in disorders of steroidogenesis, and multiplexing of androgens improves the diagnostic ability of an assay. Due to the cheap non-invasive collection, saliva is advantageous when multiple samples are required. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) offers sensitive, simultaneous quantification of steroids with short run times. Here, we have developed an LC-MS/MS assay for the simultaneous measurement of 17-hydroxyprogesterone, androstenedione, testosterone, 11 beta-hydroxyandrostenedione and 11-ketotestosterone in saliva. Methods Samples (300 mu L unstimulated whole saliva) were prepared by supported liquid extraction with dichloromethane and were reconstituted in 40% methanol. After online solid phase extraction with C18 cartridges, liquid chromatography was performed on a C8 column using a water/methanol gradient containing 0.1% formic acid and 2 mmol/L ammonium acetate. A Waters TQ-S mass spectrometer was used for quantification. Results Total run time was 6.4 min. For all analytes, recovery was between 89% and 109%, ion suppression between 86% and 105%. Intra- and inter-assay comparisons showed a coefficient of variation <10% and the bias between measured and nominal concentration varied between -8% and 10%. Interference with a large set of natural and synthetic steroids was excluded. The assay was applied for the measurement of the androgen profile in healthy men (n = 17) and women (n = 10) which confirmed the sensitivity of the assay to be appropriate. Conclusion We present a novel LC-MS/MS assay for the comprehensive profiling of classical and 11-oxygenated androgens with potential for routine clinical application.
机译:背景技术古典和11-氧化雄激素既有助于雄激素池。定期监测雄激素状态是在类定量发生的紊乱中所必需的,并且雄激素的复用改善了测定的诊断能力。由于廉价的非侵入性收集,唾液是有利的,当需要多个样品时。液相色谱 - 串联质谱(LC-MS / MS)提供敏感,同时定量类固醇,短时间内。在这里,我们开发了用于同时测量17-羟基孕酮,雄甾酮,睾酮,11β-羟基(唾液中11-酮甾体酮的LC-MS / MS测定。方法采用二氯甲烷的液体萃取制备样品(300μl未刺激的整个唾液),并在40%甲醇中重构。在用C18盒式施用在线固相萃取后,使用含有0.1%甲酸的水/甲醇梯度和2mmol / L乙酸铵在C8柱上进行液相色谱。 Waters TQ-S质谱仪用于定量。结果总运行时间为6.4分钟。对于所有分析物,回收率为89%至109%,离子抑制在86%和105%之间。分析和测定间比较显示出变异系数<10%,测量和标称浓度之间的偏差在-8%和10%之间变化。排除了大量天然和合成类固醇的干扰。施用测定用于测量健康男性(n = 17)和女性(n = 10)的雄激素曲线,这证实了测定的敏感性是合适的。结论我们提出了一种新的LC-MS / MS测定,用于常规和11-氧化雌激素的综合性探讨,具有常规临床应用的潜力。

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