Qasrawi Deema O, Pimenta Adriano M C, Petrotchenko Evgeniy V, Eintracht Shaun, Borchers Christoph H
Segal Cancer Proteomics Centre, Lady Davis Institute for Medical Research, Jewish General Hospital, McGill University, Montreal, QC H3T 1E2, Canada.
Department of Medicine, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC H4A 3J1, Canada.
Metabolites. 2025 Jan 8;15(1):30. doi: 10.3390/metabo15010030.
Quantifying urinary catecholamines and metanephrines is essential for the clinical screening and diagnosis of neuroendocrine tumours. HPLC with electrochemical detection (HPLC-ECD) is commonly used for this type of analysis but requires extensive sample cleanup. Simple and rapid dilute-and-shoot LC-multiple-reaction monitoring (MRM)-MS assays have been developed for quantitating these analytes in urine but have not yet been validated according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. A simple dilute-and-shoot sample preparation without derivatization was used. C18 RP-UPLC-MRM-MS and positive-ion ESI were used, usually with two transitions per analyte being monitored. Certified deuterated internal standards were used for each analyte. This assay was validated according to the CLSI C62-A guidelines, including accuracy/trueness, imprecision, sensitivity, specificity, carryover, stability, and linearity. The final MRM-MS method was compared to the established HPLC-ECD clinical chemistry reference method. The run time was reduced from 25 min to 5 min. A simple, robust, rapid, and cost-effective LC-MRM-MS assay for measuring urinary catecholamines and metanephrines was developed and validated according to the CLSI guidelines. This validated method requires minimal sample manipulation before analysis and provides sensitivity, specificity, and improved precision. The implementation of this assay in clinical laboratories will facilitate early and accurate diagnosis.
定量测定尿儿茶酚胺和甲氧基肾上腺素对于神经内分泌肿瘤的临床筛查和诊断至关重要。高效液相色谱-电化学检测法(HPLC-ECD)常用于此类分析,但需要对样品进行大量净化处理。已经开发出简单快速的稀释进样液相色谱-多反应监测(MRM)-质谱分析法来定量尿液中的这些分析物,但尚未按照临床和实验室标准协会(CLSI)的指南进行验证。采用了一种无需衍生化的简单稀释进样样品制备方法。使用C18反相超高效液相色谱-多反应监测-质谱联用仪和正离子电喷雾电离源,通常每种分析物监测两个跃迁。每种分析物均使用经认证的氘代内标。该分析方法按照CLSI C62-A指南进行了验证,包括准确度/真实性、不精密度、灵敏度、特异性、残留、稳定性和线性。将最终的MRM-质谱法与既定的HPLC-ECD临床化学参考方法进行了比较。运行时间从25分钟缩短至5分钟。开发了一种简单、稳健、快速且经济高效的液相色谱-多反应监测-质谱分析法,用于测定尿儿茶酚胺和甲氧基肾上腺素,并按照CLSI指南进行了验证。这种经过验证的方法在分析前所需的样品处理最少,并提供了灵敏度、特异性和更高的精密度。在临床实验室中实施该分析方法将有助于早期准确诊断。