开发并验证一种简单、快速、灵敏的液相色谱-串联质谱法,用于确定 24 小时尿游离常肾上腺素、肾上腺素和甲氧基酪胺的参考区间

IF 1.7 Q3 MEDICAL LABORATORY TECHNOLOGY Practical Laboratory Medicine Pub Date : 2024-01-23 DOI:10.1016/j.plabm.2024.e00358
Yan Song , Runhao Xu , Dan Liu , Jie Zhang
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引用次数: 0

摘要

方法 用同位素内标溶液稀释尿液样本,然后直接用串联质谱法进行分析,采用多反应监测测量和正离子模式电喷雾离子源。对该方法的线性、定量下限、不精密度和准确度等分析参数进行了评估。结果 MN、NMN 和 3-MT 的分析时间分别为 2.79、2.80 和 2.74 分钟。该方法在 1-1000 纳克/毫升的范围内显示出良好的线性关系(r > 0.99),MN 和 NMN 的定量下限(LLOQ)分别为 0.50 纳克/毫升和 0.25 纳克/毫升。该方法的日内和日间误差小于 8%。MN 的方法回收率为 96.8% 至 105.8%,NMN 为 89.7% 至 106.4%,而 3-MT 为 93.5% 至 106.2%。在对所有分析物进行分析的过程中,没有发现携带现象。采用 LC-MS/MS 方法对 81 名表面健康的志愿者的 24 小时尿样进行了参考区间测定。结论 本研究建立了一种新颖、快速、灵敏的 LC-MS/MS 方法来测定尿液中游离的儿茶酚胺代谢物,这有助于更方便快捷地筛查和诊断儿茶酚胺相关肿瘤。
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Development and validation of a simple, fast and sensitive liquid chromatography-tandem mass spectrometry method to establish reference intervals for 24-h urinary free normetanephrine, metanephrine and methoxytyramine

Objective

To develop and validate a rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to detect urinary free metanephrines and methoxytyramine, establishing reference intervals.

Methods

Urine samples were diluted with isotope internal standard solution, then analyzed directly using tandem mass spectrometry with multiple reaction monitoring measurement and electrospray ionization source in positive ion mode. Analytical parameters including linearity, lower limit of quantitation, imprecision and accuracy of the method were evaluated. The reference intervals for urinary catecholamine metabolites were established by analyzing 24-h urine samples collected from 81 apparently healthy volunteers.

Results

The analytical times for MN, NMN, and 3-MT were at 2.79, 2.80, and 2.74 min, respectively. The method displayed excellent linearity (r > 0.99) in the range of 1-1000 ng/mL, with lower limits of quantification (LLOQ) at 0.50 ng/mL for MN and NMN, and 0.25 ng/mL for 3-MT. The method's intra-day and inter-day imprecisions were less than 8 %. The method recovery ranged from 96.8% to 105.8 % for MN, 89.7%–106.4 % for NMN, and 93.5%–106.2 % for 3-MT. No carry-over was observed during the analysis of all analytes. The LC-MS/MS method was used to establish reference intervals in 24-h urine samples from 81 apparently healthy volunteers. There was no association of sex with urinary free metabolites.

Conclusion

This study established a novel, fast and sensitive LC-MS/MS method for determining urinary free catecholamine metabolites, which could facilitate screening and diagnosis for catecholamine-related tumors more conveniently and quickly.

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来源期刊
Practical Laboratory Medicine
Practical Laboratory Medicine Health Professions-Radiological and Ultrasound Technology
CiteScore
3.50
自引率
0.00%
发文量
40
审稿时长
7 weeks
期刊介绍: Practical Laboratory Medicine is a high-quality, peer-reviewed, international open-access journal publishing original research, new methods and critical evaluations, case reports and short papers in the fields of clinical chemistry and laboratory medicine. The objective of the journal is to provide practical information of immediate relevance to workers in clinical laboratories. The primary scope of the journal covers clinical chemistry, hematology, molecular biology and genetics relevant to laboratory medicine, microbiology, immunology, therapeutic drug monitoring and toxicology, laboratory management and informatics. We welcome papers which describe critical evaluations of biomarkers and their role in the diagnosis and treatment of clinically significant disease, validation of commercial and in-house IVD methods, method comparisons, interference reports, the development of new reagents and reference materials, reference range studies and regulatory compliance reports. Manuscripts describing the development of new methods applicable to laboratory medicine (including point-of-care testing) are particularly encouraged, even if preliminary or small scale.
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