Development, Estimation and Validation of Lisinopril in Bulk and its Pharmaceutical Formulation by HPLC Method

V. B. Raju, A. Rao
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引用次数: 7

Abstract

An accurate and precise HPLC method was developed for the determination of lisinopril. Separation of the drug was achieved on a reverse phase C8 column using a mobile phase consisting of phosphate buffer and methanol in the ratio of 35:65v/v. The flow rate was 0.8 mL/min and the detection wavelength was 215 nm. The linearity was observed in the range of 20-60 μ g/mL with a correlation coefficient of 0.9992. The proposed method was validated for its linearity, accuracy, precision and robustness. This method can be employed for routine quality control analysis of lisinopril in tablet dosage forms.
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赖诺普利原料药及其制剂的高效液相色谱法开发、评价与验证
建立了高效液相色谱法测定赖诺普利含量的方法。药物在反相C8柱上分离,流动相由磷酸盐缓冲液和甲醇组成,比例为35:65v/v。流速为0.8 mL/min,检测波长为215 nm。在20 ~ 60 μ g/mL范围内呈线性关系,相关系数为0.9992。该方法具有良好的线性度、准确度、精密度和鲁棒性。该方法可用于赖诺普利片剂的常规质量控制分析。
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来源期刊
E-journal of Chemistry
E-journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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