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采用自动化在线固相萃取高效液相色谱串联质谱法测定血浆游离间甲肾上腺素

Plasma free metanephrine measurement using automated online solid-phase extraction HPLC tandem mass spectrometry.

作者信息

de Jong Wilhelmina H A, Graham Kendon S, van der Molen Jan C, Links Thera P, Morris Michael R, Ross H Alec, de Vries Elisabeth G E, Kema Ido P

机构信息

Department of Pathology and Laboratory Medicine, University Medical Center, University of Groningen, Groningen, The Netherlands.

出版信息

Clin Chem. 2007 Sep;53(9):1684-93. doi: 10.1373/clinchem.2007.087114.

Abstract

BACKGROUND

Quantification of plasma free metanephrine (MN) and normetanephrine (NMN) is considered to be the most accurate test for the clinical chemical diagnosis of pheochromocytoma and follow-up of pheochromocytoma patients. Current methods involve laborious, time-consuming, offline sample preparation, coupled with relatively nonspecific detection. Our aim was to develop a rapid, sensitive, and highly selective automated method for plasma free MNs in the nanomole per liter range.

METHODS

We used online solid-phase extraction coupled with HPLC-tandem mass spectrometric detection (XLC-MS/MS). Fifty microliters plasma equivalent was prepurified by automated online solid-phase extraction, using weak cation exchange cartridges. Chromatographic separation of the analytes and deuterated analogs was achieved by hydrophilic interaction chromatography. Mass spectrometric detection was performed in the multiple reaction monitoring mode using a quadrupole tandem mass spectrometer in positive electrospray ionization mode.

RESULTS

Total run-time including sample cleanup was 8 min. Intra- and interassay analytical variation (CV) varied from 2.0% to 4.7% and 1.6% to 13.5%, respectively, whereas biological intra- and interday variation ranged from 9.4% to 45.0% and 8.4% to 23.2%. Linearity in the 0 to 20 nmol/L calibration range was excellent (R(2) > 0.99). For all compounds, recoveries ranged from 74.5% to 99.6%, and detection limits were <0.10 nmol/L. Reference intervals for 120 healthy adults were 0.07 to 0.33 nmol/L (MN), 0.23 to 1.07 nmol/L (NMN), and <0.17 nmol/L (3-methoxytyramine).

CONCLUSIONS

This automated high-throughput XLC-MS/MS method for the measurement of plasma free MNs is precise and linear, with short analysis time and low variable costs. The method is attractive for routine diagnosis of pheochromocytoma because of its high analytical sensitivity, the analytical power of MS/MS, and the high diagnostic accuracy of free MNs.

摘要

背景

血浆游离甲氧基肾上腺素(MN)和去甲氧基肾上腺素(NMN)的定量分析被认为是嗜铬细胞瘤临床化学诊断及患者随访中最准确的检测方法。目前的方法需要繁琐、耗时的离线样品制备,且检测相对缺乏特异性。我们的目标是开发一种快速、灵敏且高选择性的自动化方法,用于检测纳摩尔每升范围内的血浆游离甲氧基肾上腺素。

方法

我们采用在线固相萃取结合高效液相色谱 - 串联质谱检测(XLC - MS/MS)。使用弱阳离子交换柱,通过自动化在线固相萃取对50微升血浆当量进行预纯化。通过亲水相互作用色谱实现分析物和氘代类似物的色谱分离。使用四极杆串联质谱仪在正电喷雾电离模式下的多反应监测模式进行质谱检测。

结果

包括样品净化在内的总运行时间为8分钟。批内和批间分析变异(CV)分别在2.0%至4.7%和1.6%至13.5%之间,而生物日内和日间变异范围为9.4%至45.0%和8.4%至23.2%。在0至20纳摩尔/升的校准范围内线性良好(R²>0.99)。对于所有化合物,回收率在74.5%至99.6%之间,检测限<0.10纳摩尔/升。120名健康成年人的参考区间为0.07至0.33纳摩尔/升(MN)、0.23至1.07纳摩尔/升(NMN)以及<0.17纳摩尔/升(3 - 甲氧基酪胺)。

结论

这种用于测量血浆游离甲氧基肾上腺素的自动化高通量XLC - MS/MS方法精确且呈线性,分析时间短且可变成本低。由于其高分析灵敏度、MS/MS的分析能力以及游离甲氧基肾上腺素的高诊断准确性,该方法对嗜铬细胞瘤的常规诊断具有吸引力。

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