Salinas-Castillo A, Cañabate-Díaz B, Segura-Carretero A, Fernández-Gutiérrez A
Department of Analytical Chemistry, Faculty of Sciences, University of Granada, c/ Fuentenueva s/n, 18071 Granada, Spain.
Anal Bioanal Chem. 2007 Mar;387(5):1945-8. doi: 10.1007/s00216-006-1023-z. Epub 2007 Jan 4.
It is already recognised that heavy-atom-induced, room-temperature phosphorescence can be used to determine pindolol in pharmaceutical samples and biological fluids. We describe here a new, simple, rapid and selective development of this technique. The phosphorescence signals derive from the interaction of pindolol with a relatively high concentration of heavy-atom salts in the presence of sodium sulphite as oxygen scavenger. Phosphorescence was registered in the presence of 1.2 M potassium iodide, 15 mM sodium sulphite and 30% v/v methanol at 450 nm, exciting at 285 nm. The detection limit was 21.1 ng mL(-1). The method has been successfully applied to the determination of pindolol in commercial pharmaceutical tablets, urine and blood serum.
人们已经认识到,重原子诱导的室温磷光可用于测定药物样品和生物流体中的吲哚洛尔。我们在此描述了该技术的一种新的、简单、快速且选择性的发展。磷光信号源于在亚硫酸钠作为氧清除剂存在的情况下,吲哚洛尔与相对高浓度的重原子盐之间的相互作用。在450 nm处记录磷光,激发波长为285 nm,存在1.2 M碘化钾、15 mM亚硫酸钠和30% v/v甲醇。检测限为21.1 ng mL⁻¹。该方法已成功应用于市售药片中吲哚洛尔、尿液和血清的测定。