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分光光度法测定剂型中氢溴酸西酞普兰的方法开发与应用

Development and application of spectrophotometric methods for the determination of citalopram hydrobromide in dosage forms.

作者信息

Raza Asad

机构信息

Analytical Laboratory, Bio Fine Pharmaceuticals (Pvt.) Ltd., Multan, Pakistan.

出版信息

Chem Pharm Bull (Tokyo). 2006 Apr;54(4):432-4. doi: 10.1248/cpb.54.432.

Abstract

Study was carried out to develop two simple, fast, accurate and sensitive spectrophotometric methods (A and B) for the determination of citalopram hydrobromide in commercial tablet formulations. In method A, UV spectrophotometer determined the contents of citalopram hydrobromide in tablets at 240 nm in methanol solvent. The linear range was 5-40 microg ml-1 with molar absorptivity 1.4x10(4) l mol-1 cm-1. While the method B based on the reaction of citalopram base as n-electron donor with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone as pi-acceptors to give highly colored complex species that absorb maximally at 590 nm. Beer's law was obeyed in the concentration limit of 10-250 microg ml-1 with molar absorptivity 3.3x10(3) l mol-1 cm-1 for citalopram hydrobromide. The limits of detection and limit of quantification was calculated and found to be 5.2 microg ml-1 and 17.4 microg ml-1 respectively. The proposed methods were found to be rapid, accurate, precise and sensitive for the determination of citalopram hydrobromide in commercial tablet formulations with out interferences from common additives encountered.

摘要

开展了一项研究,以开发两种简单、快速、准确且灵敏的分光光度法(方法A和方法B),用于测定市售片剂制剂中的氢溴酸西酞普兰。在方法A中,紫外分光光度计在甲醇溶剂中于240 nm处测定片剂中氢溴酸西酞普兰的含量。线性范围为5 - 40 μg ml-1,摩尔吸光系数为1.4×10(4) l mol-1 cm-1。而方法B基于西酞普兰碱作为n电子供体与2,3 - 二氯 - 5,6 - 二氰基 - 1,4 - 苯醌作为π受体的反应,生成在590 nm处有最大吸收的高显色络合物。对于氢溴酸西酞普兰,在10 - 250 μg ml-1的浓度范围内符合比尔定律,摩尔吸光系数为3.3×10(3) l mol-1 cm-1。计算出检测限和定量限分别为5.2 μg ml-1和17.4 μg ml-1。结果发现,所提出的方法对于测定市售片剂制剂中的氢溴酸西酞普兰快速、准确、精密且灵敏,不受常见添加剂的干扰。

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