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[溶剂萃取与高效液相色谱-电化学检测法测定血浆儿茶酚胺]

[Solvent extraction and high performance liquid chromatography with electrochemical detection for determination of plasma catecholamines].

作者信息

Zhang L, Zhao W K

出版信息

Zhongguo Yao Li Xue Bao. 1989 Nov;10(6):572-5.

PMID:2641860
Abstract

This paper describes a technique for selectively extracting plasma catecholamines prior to quantification by HPLC-EC. The extraction system was a two-stage process. The first stage involve the complex formation between diphenylbrorate and catechol (diol) groups in alkaline medium. The second stage was a liquid-liquid extraction. The complex combined with tetraoctylammonium bromide to form an ion-pair formation into organic solvent. The catecholamines in turn was extracted with acid. This technique provided a very specific extraction procedure which resulted in chromatograms with few interfering compounds and gave absolute recoveries (100-103%) of norepinephrine, epinephrine and dopamine. Meanwhile, the plasma catecholamines were concentrated and the detective sensitivity was increased. A good linear relationship was found between the concentrations and ratio of peak heights of the catecholamines from 0.125-2 ng. The correlation coefficients ranged from 0.998-0.999. The coefficients of variation of the intra- and inter-assay were within 3 and 6% respectively. The results show that the procedure is very simple and fast. The method is valuable not only for clinical diagnosis but also for laboratory research.

摘要

本文描述了一种在通过高效液相色谱 - 电化学检测法(HPLC - EC)进行定量分析之前选择性提取血浆儿茶酚胺的技术。提取系统分两个阶段进行。第一阶段涉及在碱性介质中溴化二苯酯与儿茶酚(二醇)基团形成络合物。第二阶段是液 - 液萃取。该络合物与四辛基溴化铵结合形成离子对进入有机溶剂。儿茶酚胺再用酸萃取。该技术提供了一种非常特异的提取方法,其色谱图中干扰化合物很少,去甲肾上腺素、肾上腺素和多巴胺的绝对回收率为(100 - 103%)。同时,血浆儿茶酚胺得到浓缩,检测灵敏度提高。儿茶酚胺浓度与峰高比在0.125 - 2 ng之间呈良好的线性关系。相关系数在0.998 - 0.999之间。批内和批间变异系数分别在3%和6%以内。结果表明该方法非常简单快速。该方法不仅对临床诊断有价值,而且对实验室研究也有价值。

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[Solvent extraction and high performance liquid chromatography with electrochemical detection for determination of plasma catecholamines].[溶剂萃取与高效液相色谱-电化学检测法测定血浆儿茶酚胺]
Zhongguo Yao Li Xue Bao. 1989 Nov;10(6):572-5.
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