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邻苯二甲醛-亚硫酸盐柱前衍生化高效液相色谱法测定组胺

Determination of Histamine by High-Performance Liquid Chromatography After Precolumn Derivatization with o-Phthalaldehyde-Sulfite.

作者信息

Chen Rongxiang, Deng Yinghua, Yang Liu, Wang Jie, Xu Fuqiang

机构信息

Research Center for Medicine and Biology, Zunyi Medical University, Zunyi, Guizhou, 563003, P. R. China Key Laboratory of Magnetic Resonance in Biological Systems, State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan, Hubei 430071, P. R. China.

Department of Chemistry and Life Science, Hubei University of Education, Wuhan, Hubei 430205, P. R. China.

出版信息

J Chromatogr Sci. 2016 Apr;54(4):547-53. doi: 10.1093/chromsci/bmv185. Epub 2015 Dec 19.

Abstract

A fast and sensitive method was developed for in vivo determination of histamine in the brain microdialysate by reverse ion pair chromatography with electrochemical detection. The microdialysates were derivatized with o-phthalaldehyde and sodium sulfite, and separation was achieved using isocratic elution within 10 min. The separation was performed in an Agilent Eclipse Plus C18 column (3.0 × 150 mm, particle size 3.5 μm), and the mobile phase consisted of 100 mM monosodium phosphate (pH 6.0), 500 mg L(-1) OSA and 20% methanol (v/v). The linearity (R(2)) was found to be >0.999, with a range from 2 to 50 nM and excellent repeatability (relative standard deviation, 2.29-6.04%), and the limit of detection was 0.4 nM. This method was successfully applied to analyze the extracellular concentration of histamine in the hypothalamus of rats, with probe recovery calculated in vivo.

摘要

建立了一种快速灵敏的方法,通过反相离子对色谱-电化学检测法测定脑微透析液中的组胺。微透析液用邻苯二甲醛和亚硫酸钠衍生化,采用等度洗脱在10分钟内实现分离。分离在安捷伦Eclipse Plus C18柱(3.0×150 mm,粒径3.5μm)上进行,流动相由100 mM磷酸二氢钠(pH 6.0)、500 mg L(-1) OSA和20%甲醇(v/v)组成。线性关系(R(2))>0.999,范围为2至50 nM,重复性良好(相对标准偏差为2.29 - 6.04%),检测限为0.4 nM。该方法成功应用于分析大鼠下丘脑组胺的细胞外浓度,并在体内计算探针回收率。

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1
Ion Pairing Chromatography.离子对色谱法。
Crit Rev Anal Chem. 2008 Jul-Sep;38(3):161-213. doi: 10.1080/10408340802038882.

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