UHPLC-HRMS determination of adrenaline and dopamine dansyl derivatives in human saliva

Q4 Chemistry
A. Azaryan, E. Dmitrieva, A. Temerdashev
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引用次数: 1

Abstract

In the last decade, the quantification of catecholamines in human biological fluids has been of great interest. Changes in catecholamine levels, such as adrenaline and dopamine, in the body lead to neurological disorders as well as several diseases, namely Alzheimer’s and Parkinson’s diseases, neuroendocrine catecholamine - producing tumors - pheochromocytoma, paraganglioma, carcinoid tumors and neuroblastoma. Moreover, different drug combinations can lead to the distortions in the human biological passport, containing the information not only about the erythropoiesis and steroid profile, but also about catecholamine levels, which are difficult to quantify in terms of sample preparation and analysis. A method has been proposed for the determination of adrenaline and dopamine dansyl derivatives in human saliva, including the derivatization and determination of analytes by ultra-high-performance liquid chromatography (UHPLC) with high resolution mass spectrometric detection. The derivatization procedure allowed obtaining less polar catecholamine derivatives, which is especially important for their quantification by reversed-phase ultra-high-performance liquid chromatography since it ensures their better retention on the sorbent. The sensitivity of these substances quantification by the proposed method was estimated; the highest sensitivity was achieved using the mobile phase consisting of the 0.1% formic acid aqueous solution and acetonitrile. The lower limit of quantification was 5 ng/mL for dansyldrenaline and 10 ng/mL for dansyldopamine respectively. The proposed technique was tested on real saliva samples obtained from volunteers to quantify catecholamine dansyl derivatives by reversed-phase high-performance liquid chromatography with high-resolution mass spectrometric detection. High sensitivity of the technique allows using it for adrenaline and dopamine determination in clinical diagnosis.
UHPLC-HRMS法测定人唾液中肾上腺素和多巴胺的丹酰衍生物
在过去的十年里,人类生物液中儿茶酚胺的定量一直备受关注。体内儿茶酚胺水平的变化,如肾上腺素和多巴胺,会导致神经系统疾病以及几种疾病,即阿尔茨海默病和帕金森病、神经内分泌儿茶酚胺产生肿瘤——嗜铬细胞瘤、副神经节瘤、类癌和神经母细胞瘤。此外,不同的药物组合可能导致人类生物护照的扭曲,不仅包含红细胞生成和类固醇概况的信息,还包含儿茶酚胺水平的信息,这些信息在样品制备和分析方面很难量化。提出了一种测定人唾液中肾上腺素和多巴胺-丹皮酰衍生物的方法,包括超高效液相色谱法(UHPLC)和高分辨率质谱法检测分析物的衍生化和测定。衍生化程序允许获得极性较低的儿茶酚胺衍生物,这对于通过反相超高效液相色谱法对其进行定量尤其重要,因为它确保了它们在吸附剂上更好的保留。对所提出的方法定量这些物质的灵敏度进行了估计;使用由0.1%甲酸水溶液和乙腈组成的流动相获得最高灵敏度。丹西肾上腺素的定量下限分别为5 ng/mL和丹西多巴胺的定量下限为10 ng/mL。所提出的技术在志愿者的真实唾液样本上进行了测试,以通过反相高效液相色谱法和高分辨率质谱检测来量化儿茶酚胺-丹酰衍生物。该技术灵敏度高,可用于临床诊断中肾上腺素和多巴胺的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Analitika i Kontrol
Analitika i Kontrol Chemistry-Analytical Chemistry
CiteScore
0.90
自引率
0.00%
发文量
15
期刊介绍: Analitika i Kontrol is a scientific journal covering theoretical and applied aspects of analytical chemistry and analytical control, published since autumn 1997. Founder and publisher of the journal is the Ural Federal University named after the first President of Russia Boris Yeltsin (UrFU, Ekaterinburg).
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