Norouzi P, Ganjali M R, Zare M, Mohammadi A
Center of Excellence in Electrochemistry, Department of Chemistry, University of Tehran, Tehran, Iran.
J Pharm Sci. 2007 Aug;96(8):2009-17. doi: 10.1002/jps.20851.
An easy and fast Fourier transform continuous cyclic voltammetric technique for monitoring of ultra trace amounts of naltrexone in a flow-injection system has been introduced in this work. The potential waveform, consisting of the potential steps for cleaning, stripping and potential ramp, was continuously applied on an Au disk microelectrode (with a 12.5 microm in radius). The proposed detection method has some of advantages, the greatest of which are as follows: first, it is no more necessary to remove oxygen from the analyte solution and second, this is a very fast and appropriate technique for determination of the drug compound in a wide variety of chromatographic analysis methods. The method was linear over the concentration range of 0.34-34000 pg/mL (r = 0.9985) with a limit of detection 8.0 x 10(-4) nM. The method has the requisite accuracy, sensitivity, precision, and selectivity to assay naltrexone in tablets. The influences of pH of eluent, accumulation potential, sweep rate, and accumulation time on the determination of the naltrexone were considered.
本文介绍了一种简单快速的傅里叶变换连续循环伏安技术,用于在流动注射系统中监测痕量纳曲酮。由清洗、溶出和电位扫描的电位阶跃组成的电位波形连续施加于半径为12.5微米的金盘微电极上。所提出的检测方法具有一些优点,其中最大的优点如下:第一,无需从分析物溶液中去除氧气;第二,在各种色谱分析方法中,这是一种非常快速且合适的药物化合物测定技术。该方法在0.34 - 34000 pg/mL的浓度范围内呈线性(r = 0.9985),检测限为8.0×10⁻⁴ nM。该方法具有测定片剂中纳曲酮所需的准确度、灵敏度、精密度和选择性。考察了洗脱液pH值、富集电位、扫描速率和富集时间对纳曲酮测定的影响。