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基于 LC-MS/MS 的标准化甾体激素谱分析。

Standardized LC-MS/MS based steroid hormone profile-analysis.

机构信息

BIOCRATES Life Sciences AG, Innrain 66, A-6020 Innsbruck, Austria.

出版信息

J Steroid Biochem Mol Biol. 2012 Apr;129(3-5):129-38. doi: 10.1016/j.jsbmb.2011.12.001. Epub 2011 Dec 27.

Abstract

In order to overcome many limitations of immunoassays, high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) has the potential to find its place in the clinical laboratory medicine for quantification of steroid hormones. A prerequisite for the application of a new analytical procedure in clinical diagnostics is standardization to minimize analytical intra- and interlaboratory variability and inaccuracy. We evaluate a newly standardized HPLC-MS/MS assay in kit-format, developed for routine determination of 16 steroid hormones in human serum samples. Fifteen metabolites can be measured quantitatively, which include aldosterone, androstenedione, androsterone, corticosterone, cortisol, cortisone, 11-deoxycortisol, dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulfate (DHEAS), 17β-estradiol (E2), estrone (E1), etiocholanolone, 17α-hydroxyprogesterone (17OHP), progesterone, and testosterone. 11-Deoxycorticosterone is the only compound rated as semi-quantitative in this kit. The sample preparation is performed by solid phase extraction (SPE) on a 96-well plate. The standardized assay has been validated for human serum in terms of lower and upper limit of quantification (LLOQ 0.01-32 ng/mL, ULOQ 5-8000 ng/mL), linear correlation coefficient of calibration (R(2)>0.9966), intra- and inter-day precision (intra-day 1.1-8.8%, inter-day 5.2-14.8% and 8.2-18.6% for 11-deoxycorticosterone), accuracy (intra-day 88.3-115.5% and 109.3-128.2% for 11-deoxycorticosterone, inter-day 91.4-117.2% and 102.3-137.1% for 11-deoxycorticosterone), analytical total error (3.6-17.8%), proficiency test accuracy (85.4-113.4%), recovery (68-99%), and metabolite stability (freeze/thaw stability 95.5-108.1%, short term stability 86.9-107.2%). Inter-assay comparison with a routine reference HPLC-MS/MS assay and seven immunoassays demonstrates the outstanding high performance of this HPLC-MS/MS based kit by improvements in accuracy for progesterone, androstenedione, and 17OHP. Finally, results of two metyrapone tests demonstrate the potential of the standardized HPLC-MS/MS assay for the analysis of a comprehensive steroid hormone profile in clinical diagnostics.

摘要

为了克服免疫分析的许多局限性,高效液相色谱-串联质谱(HPLC-MS/MS)有可能在临床实验室医学中找到其在定量类固醇激素方面的位置。新分析程序在临床诊断中的应用的前提是标准化,以最大程度地减少分析的实验室内和实验室间变异性和不准确性。我们评估了一种新的以试剂盒形式开发的标准化 HPLC-MS/MS 分析方法,用于常规测定人血清样品中的 16 种类固醇激素。可定量测量 15 种代谢物,包括醛固酮、雄烯二酮、雄酮、皮质酮、皮质醇、可的松、11-脱氧皮质醇、脱氢表雄酮(DHEA)、脱氢表雄酮硫酸盐(DHEAS)、17β-雌二醇(E2)、雌酮(E1)、表雄酮、17α-羟孕酮(17OHP)、孕酮和睾酮。在该试剂盒中,11-脱氧皮质酮是唯一被评为半定量的化合物。样品制备通过固相萃取(SPE)在 96 孔板上进行。该标准化分析方法已针对人血清进行了验证,包括定量下限(LLOQ 0.01-32ng/mL,ULOQ 5-8000ng/mL)、校准的线性相关系数(R(2)>0.9966)、日内和日间精密度(11-脱氧皮质酮的日内 1.1-8.8%,日间 5.2-14.8%和 8.2-18.6%)、准确度(11-脱氧皮质酮的日内 88.3-115.5%和 109.3-128.2%,日间 91.4-117.2%和 102.3-137.1%)、分析总误差(3.6-17.8%)、能力验证准确度(85.4-113.4%)、回收率(68-99%)和代谢物稳定性(冻融稳定性 95.5-108.1%,短期稳定性 86.9-107.2%)。与常规参考 HPLC-MS/MS 分析方法和七种免疫分析方法的间室比较表明,该基于 HPLC-MS/MS 的试剂盒通过提高孕酮、雄烯二酮和 17OHP 的准确性,具有出色的高性能。最后,两项甲吡酮试验的结果表明,标准化 HPLC-MS/MS 分析方法在临床诊断中分析全面类固醇激素谱的潜力。

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