Application of π-acceptors to the spectrophotometric determination of lisinopril in commercial dosage forms

Nafisur Rahman, Nishat Anwar, Mohammad Kashif
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引用次数: 27

Abstract

Two simple, rapid and sensitive spectrophotometric methods have been proposed for the determination of lisinopril in pure form and pharmaceutical formulations. The methods are based on the charge transfer complexation reaction of the drug with 7,7,8,8,tetracyanoquinodimethane (TCNQ) and p-chloranilic acid (pCA) in polar media. The lisinopril–TCNQ and lisinopril–pCA charge transfer complexes dissociate in acetone and methanol, respectively, and yield coloured TCNQ and pCA radical anions which are measured spectrophotometrically at 743 and 525 nm. Under optimised experimental conditions, Beer's law is obeyed in the concentration range of 2–26 and 25–300 μg ml–1 with molar absorptivity of 1.432 × 104 and 1.192 × 104 l mol–1 cm–1 for TCNQ and pCA methods, respectively. Both the methods have been applied to the determination of lisinopril in pharmaceutical dosage forms. Results of analysis are validated statistically.

π受体在赖诺普利市售剂型分光光度测定中的应用
建立了两种简单、快速、灵敏的分光光度法测定赖诺普利纯品和制剂的含量。该方法基于该药物与7,7,8,8,四氰喹诺二甲烷(TCNQ)和对氯苯酸(pCA)在极性介质中的电荷转移络合反应。赖诺普- TCNQ和赖诺普- pCA电荷转移配合物分别在丙酮和甲醇中解离,得到TCNQ和pCA染色阴离子,分别在743和525 nm处分光光度测定。在优化的实验条件下,TCNQ法和pCA法在2-26和25-300 μg ml-1浓度范围内符合Beer定律,摩尔吸光度分别为1.432 × 104和1.192 × 104 l mol-1 cm-1。两种方法均已应用于药物剂型赖诺普利的测定。分析结果经统计学验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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