Pérez-Ruiz T, Martínez-Lozano C, Tomás V, Carpena J
Department of Analytical Chemistry, University of Murcia, Spain.
J Pharm Biomed Anal. 1998 Aug;17(4-5):719-24. doi: 10.1016/s0731-7085(97)00228-8.
A very simple, rapid and highly sensitive method is described for determining naproxen in serum and urine. This method is based on room temperature phosphorescence of naproxen in sodium dodecylsulphate micelles, with thallium(I) providing the external heavy atom and sodium sulphite acting as the oxygen scavenger. Under the optimum and experimental conditions, the range of application is 0.09-4.5 micrograms ml-1 and the limit of detection is 0.03 micrograms ml-1. The most relevant characteristic of this method is its great selectivity, e.g. naproxen can be determined in the presence of other nonsteroidal anti-inflammatory drugs (NSAIDs). The clinical applicability of this procedure has been tested, analysing naproxen in serum and urine samples. The analytical recoveries and inter- and intra assay precision data obtained demonstrate the usefulness of this procedure when used with very complex samples.
本文描述了一种测定血清和尿液中萘普生的非常简单、快速且高度灵敏的方法。该方法基于萘普生在十二烷基硫酸钠胶束中的室温磷光,铊(I)作为外部重原子,亚硫酸钠作为氧清除剂。在最佳实验条件下,应用范围为0.09 - 4.5微克/毫升,检测限为0.03微克/毫升。该方法最显著的特点是具有很高的选择性,例如可以在其他非甾体抗炎药(NSAIDs)存在的情况下测定萘普生。已对该方法的临床适用性进行了测试,分析了血清和尿液样本中的萘普生。所获得的分析回收率以及批间和批内测定精密度数据表明,该方法用于非常复杂的样本时是有用的。