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Silica stationary phase-based on-line sample enrichment coupled with LC-MS/MS for the quantification of dopamine, serotonin and their metabolites in rat brain microdialysates

机译:基于硅胶固定相的在线样品富集结合LC-MS / MS用于定量测定大鼠脑微透析液中的多巴胺,5-羟色胺及其代谢物

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摘要

Accurate measurement of trace levels of endogenous compounds remains challenging despite advancements in analytical technologies. In particular, monoamine neurotransmitters such as dopamine (DA) and serotonin (5-HT) are polar compounds with low molecular weights, which complicates the optimization of retention and detection on liquid chromatography-mass spectrometry (LC-MS). Microdialysis is an important sampling technique to collect extracellular fluid from the brain of living animals. However, the very low basal concentrations of the neurotransmitters, small sample volume (maximum 30 mL) and the absence of matrix-matching calibrators are limitations of a microdialysate as an analytical sample. In the present study, an LC-MS/MS method was developed and fully validated for the quantification of DA, 5-HT and their main metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA), in microdialysates from the rat nucleus accumbens shell. To improve the method sensitivity and accuracy, on-line sample enrichment using silica stationary phase was employed, before which any other sample pretreatment was not performed. The validation results proved the method to be selective, sensitive, accurate and precise, with acceptable linearity within calibration ranges. The lower limits of quantification were 0.025, 0.1, 0.5, 25 and 2.5 ng/mL for 5-HT, DA, 5-HIAA, HVA and DOPAC, respectively. This is a powerful analytical method to determine endogenous concentrations of those compounds in microdialysates from the rat nucleus accumbens and will be very useful to further study on the pathophysiological functions of monoamine neurotramsmitters in vivo. (C) 2016 Elsevier B.V. All rights reserved.
机译:尽管分析技术取得了进步,但准确测量痕量内源性化合物仍然具有挑战性。特别是多胺(DA)和5-羟色胺(5-HT)等单胺类神经递质是低分子量的极性化合物,这使液相色谱-质谱(LC-MS)保留和检测的优化变得复杂。微透析是从活体动物的大脑收集细胞外液的重要采样技术。但是,神经递质的基础浓度非常低,样品体积小(最大30 mL)以及缺少基质匹配的校准剂,都是微量透析液作为分析样品的局限性。在本研究中,开发了一种LC-MS / MS方法,并完全验证了DA,5-HT及其主要代谢物3,4-二羟基苯基乙酸(DOPAC),高香草酸(HVA)和5-羟基吲哚乙酸的定量伏安酸(5-HIAA),来自伏隔大鼠核壳的微透析液。为了提高方法的灵敏度和准确性,采用了使用硅胶固定相进行在线样品富集的方法,此后未进行任何其他样品预处理。验证结果证明该方法具有选择性,灵敏,准确和精确,在校准范围内具有可接受的线性。 5-HT,DA,5-HIAA,HVA和DOPAC的定量下限分别为0.025、0.1、0.5、25和2.5 ng / mL。这是确定大鼠伏隔核微透析液中这些化合物内源浓度的有力分析方法,对于进一步研究体内单胺神经递质的病理生理功能非常有用。 (C)2016 Elsevier B.V.保留所有权利。

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