Stubauer G, Obendorf D
Institut für Analytische Chemie und Radiochemie, der Universität Innsbruck, Austria.
Analyst. 1996 Mar;121(3):351-6. doi: 10.1039/an9962100351.
A relatively simple electroanalytical procedure for the determination of niguldipine in biological samples is described. The technique involves adsorptive accumulation of the drug at the hanging mercury drop electrode (HMDE) followed by a differential-pulse polarographic determination of the preconcentrated species. The adsorptive stripping response is evaluated with respect to various experimental conditions, such as solvent composition and pH of the supporting electrolyte, accumulation potential and accumulation time. After a simple sample preparation, the method can be used for the determination of niguldipine in blood and urine. Interfering substances are simply removed by precipitation, adding a small amount of 5% ZnSO4 solution and ethanol to the urine or blood sample and centrifuging the mixture. A limit of detection of 6.7 ng per ml of urine and 41 ng per ml of blood is found with a mean recovery of 96% in urine and 71% in blood. The mean relative errors are 8.4% and 2.2%, respectively.
本文描述了一种用于测定生物样品中尼群地平的相对简单的电分析方法。该技术包括药物在悬汞滴电极(HMDE)上的吸附富集,然后对预富集的物质进行差分脉冲极谱测定。针对各种实验条件,如溶剂组成、支持电解质的pH值、富集电位和富集时间,对吸附溶出响应进行了评估。经过简单的样品制备后,该方法可用于测定血液和尿液中的尼群地平。通过沉淀简单地去除干扰物质,向尿液或血液样品中加入少量5%的硫酸锌溶液和乙醇,然后将混合物离心。发现尿液的检测限为每毫升6.7纳克,血液的检测限为每毫升41纳克,尿液中的平均回收率为96%,血液中的平均回收率为71%。平均相对误差分别为8.4%和2.2%。