Brandsteterová E, Kubalec P, Skacáni I, Balazovjech I
Department of Analytical Chemistry, Slovak Technical University, Bratislava.
Neoplasma. 1994;41(4):205-11.
High performance liquid chromatography (HPLC) with electrochemical detection (ED) was applied for the monitoring of catecholamines (epinephrine - E, norepinephrine - NE, dopamine - DA) and their main metabolites (homovanillic acid - HVA, vanillylmandelic acid - VMA) in urine samples of patients with the pheochromocytoma diagnosis. Both amperometric and colorimetric detectors were tested for the clinical applications and the results were compared. The optimization of separation conditions was worked out, especially the effects of mobile phase compositions (pH, ionic strength, organic modifier and ion-pair agent concentrations). Dependences of capacity ratio values k' on all optimized components of the mobile phases were evaluated. Chromatographic conditions were optimized for the suitable chromatographic resolution (Rij > 1.25). Extraction recoveries for liquid-liquid and solid-phase extractions have been worked-out. Detection limits for catecholamines in urine were in the range of 0.3-0.6 ng/ml and 10-20 ng/ml for HVA, VMA using coulometric detector.
采用高效液相色谱法(HPLC)结合电化学检测(ED)对嗜铬细胞瘤诊断患者的尿液样本中的儿茶酚胺(肾上腺素 - E、去甲肾上腺素 - NE、多巴胺 - DA)及其主要代谢产物(高香草酸 - HVA、香草扁桃酸 - VMA)进行监测。对电流型和比色型检测器都进行了临床应用测试,并对结果进行了比较。确定了分离条件的优化方法,特别是流动相组成(pH值、离子强度、有机改性剂和离子对试剂浓度)的影响。评估了容量比值k'对流动相所有优化组分的依赖性。针对合适的色谱分辨率(Rij > 1.25)对色谱条件进行了优化。确定了液 - 液萃取和固相萃取的萃取回收率。使用库仑检测器时,尿液中儿茶酚胺的检测限在0.3 - 0.6 ng/ml范围内,HVA、VMA的检测限在10 - 20 ng/ml范围内。