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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Quantification of monoamine neurotransmitters and melatonin in sea lamprey brain tissues by high performance liquid chromatography-electrospray ionization tandem mass spectrometry
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Quantification of monoamine neurotransmitters and melatonin in sea lamprey brain tissues by high performance liquid chromatography-electrospray ionization tandem mass spectrometry

机译:高效液相色谱-电喷雾电离串联质谱法定量测定海七rey鳗脑组织中单胺类神经递质和褪黑激素

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摘要

A rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous quantification of three monoamine neurotransmitters (NTs) and melatonin in sea lamprey brain tissues. Separation was performed on a reversed-phase column with mobile phases of 1 mM perfluoroheptanoic acid (PFHA) water solution/acetonitrile and mass spectra were acquired in positive electrospray ionization multiple reaction monitoring (MRM) mode. Solid-phase extraction (SPE) was employed to purify and extract the target compounds from the tissue samples. The matrix effects as well as the influence of two extraction methods, protein precipitation (PPT) and SPE, on matrix effects were examined for the first time on the quantification of NTs from brain tissue extracts. The matrix effects with SPE (2.4 to -14.9%) were about 30% lower on average than those with the ACN PPT method (-29 to -38%). The recoveries of three types of SPE cartridges were tested and Bond-Elut C18 cartridge was selected to process the samples because of its good extraction efficiencies (71.3-95.3%) and low matrix effects (-6.6 to -14.9%) for all four analytes. This method exhibited excellent linearity for all analytes with regression coefficients higher than 0.99. The limits of detection were between 0.03 ng/mL (melatonin) and 0.14 ng/mL (norepinephrine). The precisions, expressed as coefficients of variation (CV), ranged from 4.8 to 14.1% for intra-day analyses and from 6.1 to 16.2% for inter-day analyses. Brain tissues from 360 sea lampreys were analyzed by the developed method and the concentrations for four analytes were found to be at the level of nanogram per gram of brain tissues. To our knowledge, this is the first report on the quantification of NTs and melatonin in the sea lamprey using the LC-MS/MS method.
机译:建立了快速液相色谱-串联质谱(LC-MS / MS)方法,并进行了验证,可同时定量测定海七lamp树脑组织中的三种单胺神经递质(NTs)和褪黑激素。在流动相为1 mM全氟庚酸(PFHA)水溶液/乙腈的反相柱上进行分离,并以正电喷雾电离多反应监测(MRM)模式获取质谱。固相萃取(SPE)用于从组织样品中纯化和提取目标化合物。首次检查了基质效应以及两种提取方法(蛋白质沉淀(PPT)和SPE)对基质效应的影响,以定量脑组织提取物中的NT。与使用ACN PPT方法(-29至-38%)相比,使用SPE的基质效应(2.4至-14.9%)平均降低约30%。测试了三种类型的SPE柱的回收率并选择了Bond-Elut C18柱来处理样品,因为它对所有四种分析物均具有良好的萃取效率(71.3-95.3%)和低基质效应(-6.6至-14.9%) 。该方法对所有分析物均具有优异的线性,回归系数高于0.99。检测限在0.03 ng / mL(褪黑激素)至0.14 ng / mL(去甲肾上腺素)之间。日内分析的精度以变异系数(CV)表示,范围为4.8%至14.1%,日间分析的精度为6.1%至16.2%。通过开发的方法分析了来自360只海鳗的脑组织,发现四种分析物的浓度为每克脑组织纳克水平。据我们所知,这是有关使用LC-MS / MS方法定量分析海七rey中NT和褪黑激素的第一份报告。

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