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固相萃取-串联质谱联用快速定量检测尿中儿茶酚胺和总甲氧基肾上腺素

Solid-Phase Extraction Coupled to Tandem Mass Spectrometry for Rapid Quantitation of Urinary Catecholamines and Total Metanephrines.

作者信息

Li Yuhan, Huang Guangming

机构信息

Department of Cardiology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.

Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei, Anhui, China.

出版信息

Rapid Commun Mass Spectrom. 2025 Sep 15;39(17):e10077. doi: 10.1002/rcm.10077.

Abstract

RATIONALE

The measurement of urinary catecholamines and total metanephrines serves as one of the primary tests in the diagnosis of pheochromocytoma and paraganglioma (PPGL). The widely adopted liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, however, typically necessitates sample pretreatments and chromatographic separation prior to MS, resulting in challenges for facile and rapid screening of targets from complex matrices. Therefore, it is crucial to develop an analytical method that can rapidly and efficiently detect urinary catecholamines and total metanephrines.

METHODS

A rapid and time-efficient procedure using solid-phase extraction (SPE) combined with pulsed direct current electrospray ionization tandem mass spectrometry (pulsed-dc-ESI-MS/MS) was validated for the specific and quantitative analysis of six urinary catecholamines and metanephrines. The SPE protocol was specifically optimized to enable direct analysis of the eluate obtained from SPE using MS/MS. All six compounds could be detected in a single complete operation.

RESULTS

The method was evaluated by the determination of catecholamines and metanephrines (dopamine, epinephrine, norepinephrine, normetanephrine, metanephrine, and 3-methoxytyramine) in artificial urine samples and raw urine samples. Under the optimized experimental conditions, the limits of detection for these six analytes were in the range of 0.02-68.37 nM L, using dopamine-d4 (DA-d4) and metanephrines-d3 (MN-d3) as internal standards, respectively, which achieved the detection requirements for the clinical diagnosis of PPGL.

CONCLUSIONS

SPE coupled with pulsed-dc-ESI-MS/MS demonstrated improved efficiency compared to existing methods, which successfully enabled the rapid screening of urinary catecholamines and total metanephrines. Therefore, we believe that this method could be potentially useful in the clinical screening of PPGL and suitable for the direct analysis of urine.

摘要

原理

尿儿茶酚胺和总甲氧基肾上腺素的测定是嗜铬细胞瘤和副神经节瘤(PPGL)诊断的主要检测方法之一。然而,广泛采用的液相色谱 - 串联质谱法(LC - MS/MS)通常在质谱分析之前需要进行样品预处理和色谱分离,这给从复杂基质中简便快速地筛选目标物带来了挑战。因此,开发一种能够快速高效地检测尿儿茶酚胺和总甲氧基肾上腺素的分析方法至关重要。

方法

使用固相萃取(SPE)结合脉冲直流电喷雾电离串联质谱法(pulsed - dc - ESI - MS/MS)的快速且省时的程序,针对六种尿儿茶酚胺和甲氧基肾上腺素进行了特异性和定量分析验证。对SPE方案进行了专门优化,以便能够使用MS/MS直接分析从SPE获得的洗脱液。所有六种化合物都可以在一次完整操作中检测到。

结果

通过测定人工尿液样品和原始尿液样品中的儿茶酚胺和甲氧基肾上腺素(多巴胺、肾上腺素、去甲肾上腺素、去甲变肾上腺素、变肾上腺素和3 - 甲氧基酪胺)对该方法进行了评估。在优化的实验条件下,以多巴胺 - d4(DA - d4)和甲氧基肾上腺素 - d3(MN - d3)分别作为内标,这六种分析物的检测限在0.02 - 68.37 nM/L范围内,达到了PPGL临床诊断的检测要求。

结论

与现有方法相比,SPE与pulsed - dc - ESI - MS/MS联用显示出更高的效率,成功实现了尿儿茶酚胺和总甲氧基肾上腺素的快速筛选。因此,我们认为该方法在PPGL的临床筛查中可能具有潜在用途,并且适用于尿液的直接分析。

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