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首页> 外文期刊>Analytica chimica acta >Quantitative metabolic profiling of 21 endogenous corticosteroids in urine by liquid chromatography-triple quadrupole-mass spectrometry
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Quantitative metabolic profiling of 21 endogenous corticosteroids in urine by liquid chromatography-triple quadrupole-mass spectrometry

机译:液相色谱-三重四极杆质谱法测定尿液中21种内源性皮质类固醇的代谢谱

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Since corticosteroid metabolism may be affected by disease states, the accurate and precise measurement of endogenous corticosteroids in urine is necessary to understand their biochemical roles. An efficient quantitative profiling of 21 endogenous corticosteroids in urine has been validated by liquid chromatography-tandem mass spectrometry (LC-MS/MS). After enzymatic hydrolysis with β-glucuronidase, samples were purified using a solid-phase extraction cartridge and then separated through a sub-2 μm particle C18 column (2.1 mm x 50 mm, 1.9 μm) and quantified within 12.1 min using a triple quadrupole MS with electrospray ionization in positive ion mode. All corticosteroids resulted in the base-line separation, which is even achieved for stereo-isomers, such as α-/β-cortol, α-/β-cortolone, and allo-tetrahydrocortisol/tetrahydrocortisol. Overall recoveries ranged from 85% to 106% with limit of quantification ranged from 0.5 to 2.0 ng mL~(-1) for the corticosteroids examined. The precision (% CV) and accuracy (% bias) of the assay were 1.7-7.8% and 95.1-105.4%, respectively, in 0.5-200 ngmL~(-1) calibration ranges (r~2 > 0.9903), for quality-control samples containing 21 endogenous corticosteroids at three different urinary concentrations. Clinical application included quantitative analysis from patients with both prostate cancer and benign prostatic hyperplasia with altered Cortisol concentrations. The described LC-MS/MS method eliminates interference from other urine components, has excellent chromatographic resolution achieved by a small particle LC column with a sufficient sensitivity to allow the profiling of both gluco- and mineralo-corticosteroids at a time.
机译:由于皮质类固醇的代谢可能受疾病状态的影响,因此尿液中内源性皮质类固醇的准确和精确测量对于了解其生化作用是必要的。液相色谱-串联质谱法(LC-MS / MS)验证了尿液中21种内源性皮质类固醇的有效定量分析。用β-葡萄糖醛酸苷酶酶促水解后,使用固相萃取柱纯化样品,然后通过亚2μm粒径的C18柱(2.1 mm x 50 mm,1.9μm)分离,并在12.1分钟内使用三重四极杆MS进行定量在正离子模式下进行电喷雾电离。所有皮质类固醇都会导致基线分离,甚至对于立体异构体(例如α-/β-皮质醇,α-/β-皮质酮和别-四氢皮质醇/四氢皮质醇)都可以实现基线分离。所检测的皮质类固醇的总回收率为85%至106%,定量限为0.5至2.0 ng mL〜(-1)。在0.5-200 ngmL〜(-1)的校准范围内(r〜2> 0.9903),测定的精密度(%CV)和准确性(%偏差)分别为1.7-7.8%和95.1-105.4% -对照样品,其中包含21种内源性皮质类固醇激素,尿液浓度为三种不同。临床应用包括对前列腺癌和良性前列腺增生患者皮质醇浓度变化的定量分析。所描述的LC-MS / MS方法消除了来自其他尿液成分的干扰,通过小粒径LC色谱柱具有出色的色谱分离度,并且具有足够的灵敏度,可以同时分析糖皮质激素和矿物质-皮质类固醇。

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