Instituto de Química de San Luis, Consejo Nacional de Investigaciones Científicas y Técnicas-Universidad Nacional de San Luis, Facultad de Química, Bioquímica y Farmacia, Bloque III, Avenida Ejército de los Andes 950, San Luis CP 5700, Argentina.
Área de Toxicología, Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Calle 47 y 115, La Plata, Provincia de Buenos Aires CP 1900, Argentina.
Talanta. 2015 Jan;131:656-60. doi: 10.1016/j.talanta.2014.08.040. Epub 2014 Aug 23.
Monitoring the drug benznidazole in biological fluids is a powerful tool for clinical diagnostic and pharmacological studies in chagasic patients. However, research in this concern needs to be done. The accurate quantitation of this drug in complex matrices represents a highly challenging task complicated by the absence of sensitive analytical methods. It follows that sample processing strategies, preparation/cleanup procedures, and chromatographic/ionization/detection parameters, were evaluated for method optimization. The summation of this work generated a rapid, selective, sensitive methodology based on reversed-phase chromatography-tandem mass spectrometry for the analysis of benznidazole in urine samples. To the best of our knowledge, this is a first report of a LC-MS/MS platform employed for this application. Matrix effect was determined; a 90% of signal suppression was observed. The limits of detection and quantification were 0.75 and 4.85 μg L(-1); respectively. The latter allowed the method's application to the detection of benznidazole in clinical studies and pharmacological monitoring analysis.
监测生物体液中的药物苯并咪唑是一种强大的工具,可用于恰加斯病患者的临床诊断和药理学研究。然而,在这方面的研究需要进行。在复杂基质中准确定量这种药物是一项极具挑战性的任务,因为缺乏敏感的分析方法而变得更加复杂。因此,评估了样品处理策略、制备/净化程序以及色谱/离子化/检测参数,以优化方法。这项工作的综合结果产生了一种基于反相色谱-串联质谱的快速、选择性、灵敏的方法,用于尿液样品中苯并咪唑的分析。据我们所知,这是首次报道将 LC-MS/MS 平台应用于该应用。测定了基质效应,观察到 90%的信号抑制。检测限和定量限分别为 0.75 和 4.85μg L(-1);分别。后者允许该方法应用于临床研究和药物监测分析中苯并咪唑的检测。