Walash M I, Belal F, El-Enany N, El-Mansi H
Department of Analytical Chemistry, Faculty of Pharmacy, University of Mansoura, Mansoura, 35516, Egypt.
Int J Biomed Sci. 2010 Sep;6(3):252-9.
A simple and sensitive spectrophotometric method was developed for the determination of each of sertraline (SER) and paroxetine HCl (PXT) in dosage forms. The method is based upon reaction of PXT and SER with 2,4-dinitrofluorobenzene (DNFB) to form colored products. The absorbance of the products were measured at 375and 390 nm for SER and PXT respectively. The absorbance concentration plots were rectilinear over the concentration rang of 1-10 and 2-20 μg/mL with lower detection limits (LOD) of 0.11 and 0.28 μg/mL and quantification limits (LOQ) of 0.32 and 0.85 μg/mL for SER and PXT, respectively. The developed method was successfully applied for the determination of SER and PXT in dosage forms. The common excipients and additives did not interfere in their determinations. There was no significant difference between the results obtained by the proposed and the reference methods regarding Student t-test and the variance ratio F-test respectively. A proposal of the reaction pathway was postulated.
开发了一种简单灵敏的分光光度法,用于测定剂型中舍曲林(SER)和盐酸帕罗西汀(PXT)的含量。该方法基于PXT和SER与2,4-二硝基氟苯(DNFB)反应形成有色产物。分别在375和390nm处测定SER和PXT产物的吸光度。吸光度-浓度曲线在1-10和2-20μg/mL的浓度范围内呈线性,SER和PXT的检测限(LOD)分别为0.11和0.28μg/mL,定量限(LOQ)分别为0.32和0.85μg/mL。所开发的方法成功应用于剂型中SER和PXT的测定。常见的辅料和添加剂不干扰其测定。分别通过学生t检验和方差比F检验,所提出的方法与参考方法得到的结果之间没有显著差异。推测了反应途径。