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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous quantification of 17α-OH progesterone, 11-deoxycortisol, Δ4-androstenedione, cortisol and cortisone in newborn blood spots using liquid chromatography-tandem mass spectrometry
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Simultaneous quantification of 17α-OH progesterone, 11-deoxycortisol, Δ4-androstenedione, cortisol and cortisone in newborn blood spots using liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法同时定量新生儿血斑中的17α-OH孕酮,11-脱氧皮质醇,Δ4-雄烯二酮,皮质醇和可的松

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摘要

Adrenal steroid profiling, including 17α-OH progesterone (17OHP), 11-deoxycortisol (S), Δ4-androstenedione (Δ4-A) and cortisol (F) in blood spots by tandem mass spectrometry, is used for newborn screening to detect congenital adrenal hyperplasia (CAH). Pre-analytical sample processing is critical for assay specificity and accuracy; however, it is laborious and time-consuming. This study describes the development and validation of a new Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) method for the simultaneous quantification of five steroids: 17OHP, S, Δ4-A, F and cortisone (E) in blood spots from newborns. Whole blood was eluted from a 5.00. mm dried blood spot by an aqueous solution containing the deuterium-labeled internal standards d8-17OHP and d4-cortisol. The steroids extracted from blood spot into aqueous solution were subsequently purified via Extelut mini NT1 column using diethylether. The extracts were evaporated and quantified using LC-MS/MS. The detection limit was 0.25. ng/mL for 17OHP and S, 0.4. ng/mL for Δ4-A and 0.5. ng/mL for F and E. The limit of quantification was 0.5. ng/mL for 17OHP, S and Δ4-A and 1. ng/mL for F and E. Precision for 17OHP, S, Δ4-A at concentrations of 0.5, 2, and 8. ng/mL (n= 5) in fortified steroid free serum samples was 1.3-3.5% (intra-assay CV) and 7-14.8% (inter-assay CV). Precision for F and E at concentrations of 5 and 20. ng/mL was 1.5-4.8% (intra-assay, CV%) and 6-15% (inter-assay, CV%). Accuracy was calculated at concentrations of 0.5, 2, and 8. ng/mL for 17OHP, S and Δ4-A and ranged from -0.3 to 0.2%, while for F and E it ranged from -3.2 to 0.2%. Relative recoveries at concentration 2. ng/mL and 8. ng/mL for 17OHP, S, Δ4-A and at 5. ng/mL and 20. ng/mL for F and E ranged from 55% to 80%. Reference intervals were estimated for all steroids in newborns (on day 3). The steroid profile assay herein described is sensitive, specific and accurate and involves a simple pre-analytical sample manipulation; it is therefore suitable for routine analysis and provides data for samples within normal range as well as those with elevated levels. For the first time to our knowledge, cortisone levels are reported in dried blood spots from newborns.
机译:串联质谱法测定血液斑点中的肾上腺类固醇谱,包括17α-OH孕酮(17OHP),11-脱氧皮质醇(S),Δ4-雄烯二酮(Δ4-A)和皮质醇(F),用于新生儿筛查以检测先天性肾上腺增生(CAH)。分析前样品处理对于测定的特异性和准确性至关重要。然而,这是费力且费时的。这项研究描述了一种新的液相色谱-串联质谱(LC-MS / MS)方法的开发和验证,该方法可同时定量来自血红蛋白斑点中的五种类固醇:17OHP,S,Δ4-A,F和可的松(E)新生儿。全血从5.00洗脱。用含有氘标记的内标d8-17OHP和d4-皮质醇的水溶液干燥血斑。从血斑中提取到水溶液中的类固醇随后通过二乙醚通过Extelut mini NT1柱进行纯化。蒸发提取物并使用LC-MS / MS定量。检出限为0.25。 ng / mL的17OHP和S为0.4。对于Δ4-A和0.5为ng / mL。 F和E为ng / mL。定量限为0.5。对于17OHP,S和Δ4-A为ng / mL,对于F和E为1. ng / mL。对于浓度为0.5、2和8的17OHP,S,Δ4-A,精度为ng / mL(n = 5)。强化的不含类固醇的血清样本为1.3-3.5%(测定内CV)和7-14.8%(测定间CV)。浓度为5和20时F和E的精密度为ng / mL,为1.5-4.8%(测定内,CV%)和6-15%(测定间,CV%)。对于17OHP,S和Δ4-A,在0.5、2和8 ng / mL的浓度下计算出准确度,范围为-0.3至0.2%,而对于F和E,范围为-3.2至0.2%。 17OHP,S,Δ4-A的浓度为2. ng / mL和8. ng / mL时的相对回收率,F和E的浓度为5. ng / mL和20 ng / mL时的相对回收率在55%至80%之间。估计新生儿中所有类固醇的参考间隔(第3天)。本文所述的类固醇激素谱测定法灵敏,特异且准确,涉及简单的分析前样品操作。因此,它适用于常规分析,并提供正常范围内以及高水平样品的数据。据我们所知,首次报道了新生儿干血斑中可的松的水平。

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