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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >An improved microbore UHPLC method with electrochemical detection for the simultaneous determination of low monoamine levels in in vivo brain microdialysis samples
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An improved microbore UHPLC method with electrochemical detection for the simultaneous determination of low monoamine levels in in vivo brain microdialysis samples

机译:一种改进的具有电化学检测的微孔UHPLC方法,用于同时测定体内脑微透析样品中的低单胺水平

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摘要

The simultaneous determination of the monoamines dopamine (DA), noradrenaline (NA) and serotonin (5-HT) in in vivo microdialysis samples remains challenging because of the low extracellular neurotransmitter levels in different brain regions, specific sample characteristics, and the quest for high temporal resolution and a multi-target strategy in neuropharmacological research. A fast and sensitive microbore (1.0mm i.d. column) UHPLC method coupled to electrochemical detection (ECD) is developed by means of design of experiments with the emphasis on sufficient retention of NA within an acceptable total analysis time. Indeed, NA is the earliest eluting compound and often interferes with the broad solvent front originating from the sample matrix. The sensitive UHPLC-ECD assay (LLOQ of 100 pM for NA and 150 pM for DA and 5-HT) with an analysis time of 8 min for standard solutions and 20 min for in vivo microdialysis samples originating from rat hippocampus, prefrontal cortex and striatum, is validated applying accuracy profiles. The combination of in vivo microdialysis and microbore UHPLC-ECD has shown to be particularly suitable for future contributions to neuropharmacological research on the monoaminergic system. (C) 2016 Elsevier B.V. All rights reserved.
机译:由于不同大脑区域的细胞外神经递质水平低,特定的样品特征以及对高剂量的追求,因此在体内微量透析样品中同时测定单胺多巴胺(DA),去甲肾上腺素(NA)和血清素(5-HT)仍然具有挑战性。时间分辨率和神经药理学研究中的多目标策略。通过实验设计,开发了一种快速灵敏的微孔(内径为1.0mm的色谱柱)UHPLC方法,并结合了电化学检测(ECD),重点是在可接受的总分析时间内充分保留NA。实际上,NA是最早的洗脱化合物,通常会干扰源自样品基质的广泛溶剂前沿。灵敏的UHPLC-ECD检测(NA的LLOQ为100 pM,DA和5-HT的LLOQ为150 pM),标准溶液的分析时间为8分钟,而源自大鼠海马,前额叶皮层和纹状体的体内微透析样品的分析时间为20分钟已通过应用精度配置文件进行了验证。体内微透析和微孔UHPLC-ECD的结合已被证明特别适合于未来对单胺能系统神经药理学研究的贡献。 (C)2016 Elsevier B.V.保留所有权利。

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