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Validation of an improved liquid chromatography tandem mass spectrometry method for rapid and simultaneous analysis of plasma catecholamine and their metabolites

化学 色谱法 液相色谱-质谱法 串联质谱法 质谱法 儿茶酚胺 串联 医学 内科学 复合材料 材料科学
作者
Songlin Yu,Yicong Yin,Qianqian Li,Jialei Yu,Wenjing Liu,Danchen Wang,Qian Cheng,Shaowei Xie,Xinqi Cheng,Ling Qiu
出处
期刊:Journal of Chromatography B [Elsevier BV]
卷期号:1129: 121805-121805 被引量:25
标识
DOI:10.1016/j.jchromb.2019.121805
摘要

Catecholamines [dopamine (DA), epinephrine (E), and norepinephrine (NE)] and their metabolites [metanephrine (MN), normetanephrine (NMN), and 3-methoxytyramine (3-MT)] are functionally important in humans. Their overexpression can indicate the presence of neuroendocrine tumors. Accurate and rapid quantitation of catecholamines and their metabolites may function in differential diagnosis of neuroendocrine tumors. Herein, we diluted 200 μL plasma using isotope labelled internal standards (IS), and extracted using solid phase extraction. The performance of isotope diluted liquid chromatography tandem mass spectrometry (ID-LC-MS/MS) was evaluated and applied to quantify the level of catecholamines and metabolites in clinical samples from 73 apparently healthy adults. The total analysis time of the ID-LC-MS/MS method was 4 min. The improved method was highly sensitive, with a limit of quantification (LOQ) for MN, NMN, 3-MT, and E of 1 pg/mL, a LOQ for DA of 5 pg/mL, and for NE of 10 pg/mL. After correction using IS, no significant matrix effects were observed. Good reproducibility was obtained, with total CVs of 3.2–13.1% (DA), 4.8–10.0% (E), 6.2–6.9% (NE), 3.8–7.9% (MN), 4.1–8.8% (NMN), 3.4–8.9% (3-MT). Recoveries were in the range of 91.1–109.7% for the six analytes. Also, the mean concentration of catecholamines were as follows: MN, 22.9 ± 7.2 pg/mL; NMN, 41.4 ± 17.2 pg/mL; 3-MT, 2.34 ± 2.01 pg/mL; DA, 10.2 ± 4.6 pg/mL; E, 29.3 ± 14.2 pg/mL and NE 427.0 ± 190.6 pg/mL. A reliable ID-LC-MS/MS method for the determination of catecholamines and their metabolites using small volumes of plasma was verified. This method is rapid, simple, and may serve as an essential diagnostic tool for neuroendocrine tumors in clinical practice.
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