el-Zeany B A, Moustafa A A, Farid N F
Department of Analytical Chemistry, Faculty of Pharmacy, Cairo University, 23 El-ahrar St., Cairo, Egypt.
J Pharm Biomed Anal. 2003 Nov 24;33(4):775-82. doi: 10.1016/s0731-7085(03)00234-6.
Two spectrophotometric methods for the determination of imipramine in presence of iminodibenzyl as an impurity are described. The first method is a ratio-spectra first derivative spectrophotometry, the signals were measured at 240.2 nm for imipramine. Calibration graph was found linear in the range 5-30 microg ml(-1). The second method is based on the reaction of imipramine base, being an electron donor, with p-chloranilic acid, being pi acceptor, to form a purple colored charge transfer complex. The absorbance was measured at 520.5 nm without interference with iminodibenzyl. Both methods are rapid, simple and do not require any preliminary separation or treatment of the samples. Furthermore, the two methods were applied to pharmaceutical dosage form.
描述了两种在存在杂质亚氨基二苄的情况下测定丙咪嗪的分光光度法。第一种方法是比率光谱一阶导数分光光度法,丙咪嗪的信号在240.2 nm处测量。校准曲线在5-30μg ml⁻¹范围内呈线性。第二种方法基于作为电子供体的丙咪嗪碱与作为π受体的对氯苯醌反应,形成紫色电荷转移络合物。在520.5 nm处测量吸光度,不受亚氨基二苄的干扰。两种方法都快速、简单,不需要对样品进行任何预分离或处理。此外,这两种方法都应用于药物剂型。