Ye W, Yin P, Mei Z
Shanghai Institute of Physiology, the Chinese Academy of Sciences, Shanghai, 200031.
Se Pu. 1997 May;15(3):185-8.
In the present work, the method of microbore liquid chromatography(MLC) with dual electrode electrochemical detection (DEED) was used to determine the monoamine transmitters and their metabolites in the striatal microdialysates from the anaesthetized rats. The potentials applied on the upstream (anodic) electrode and downstream (cathodic) electrode were set at +0.72V and +0.05V versus an Ag/AgCl reference electrode respectively. The interference of the large early-eluting peaks from brain dialysate was well eliminated on cathodic detection on the basis of electrochemical reversibility of catechol compounds. The collection efficiency of catecholamine (NA, A and DA) and DOPAC, that is the ratio of their responses in downstream electrode to those in upstream, was found to be in the range of 0.690 to 0.768, thereby providing reliable identification and measurement of early elutes. MLC-DEED is one of the best methods for the determination of monoamine transmitters at trace level. To optimize separation and detection, these adaptations were made to the system with respect to the injection valve, flow rate of the pump, connections between injector, column and detector, and cell volume of the detector. The detection limit could reach 1pg or less per injection, and the amounts, at least in the range of 2-200pg, were linearly correlated with the peak areas both at anodic detection and at cathodic detection. Prior to the collection of samples the probe recovery was measured in vitro at room temperature, and the recovery (%) for NA, DA, DOPAC, 5-HIAA, 5-HT and HVA were 19.5, 18.9, 22.1, 14,6, 16.5 and 19.3 respectively. The reported concentration of each compound was corrected according to probe recovery. The basal concentration of DA and 5-HT in striatal microdialysates was 12.5 +/- 1.8 and 5.0 +/- 0.7nmol/L. The perfussion of high K+ (100 mmol/L) through the dialysis probe induced a large increase of the concentration of NA, DA and 5-HT in microdialysates, and further increase of the concentration was observed in rat postmortem. The critical points for MLC-DEED are briefly discussed.
在本研究中,采用微径液相色谱(MLC)结合双电极电化学检测(DEED)的方法,测定麻醉大鼠纹状体微透析液中的单胺类递质及其代谢产物。相对于Ag/AgCl参比电极,施加在上游(阳极)电极和下游(阴极)电极上的电位分别设定为+0.72V和+0.05V。基于儿茶酚化合物的电化学可逆性,在阴极检测时,脑透析液中较大的早洗脱峰的干扰被很好地消除。发现儿茶酚胺(去甲肾上腺素、肾上腺素和多巴胺)和3,4-二羟基苯乙酸(DOPAC)的收集效率,即它们在下游电极与上游电极中的响应之比,在0.690至0.768范围内,从而为早洗脱物提供了可靠的鉴定和测量。MLC-DEED是测定痕量单胺类递质的最佳方法之一。为了优化分离和检测,对系统在进样阀、泵流速、进样器、色谱柱和检测器之间的连接以及检测器的池体积方面进行了这些调整。每次进样的检测限可达1pg或更低,并且至少在2 - 200pg范围内,阳极检测和阴极检测时的量与峰面积均呈线性相关。在采集样品之前,在室温下体外测量探针回收率,去甲肾上腺素、多巴胺、DOPAC、5-羟吲哚乙酸(5-HIAA)、5-羟色胺(5-HT)和高香草酸(HVA)的回收率(%)分别为19.5、18.9、22.1、14.6、16.5和19.3。根据探针回收率对每种化合物的报告浓度进行校正。纹状体微透析液中多巴胺和5-羟色胺的基础浓度分别为12.5±1.8和5.0±0.7nmol/L。通过透析探针灌注高钾(100 mmol/L)导致微透析液中去甲肾上腺素、多巴胺和5-羟色胺的浓度大幅增加,并且在大鼠死后观察到浓度进一步升高。简要讨论了MLC-DEED的关键点。