High-performance liquid chromatographic assay of quinapril in tablets

Pharmaceutica acta Helvetiae Pub Date : 1998-12-01 Epub Date: 1999-01-23 DOI:10.1016/S0031-6865(98)00019-3
Anna Gumieniczek, Hanna Hopkala
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引用次数: 7

Abstract

A new, simple and accurate high-performance liquid chromatography (HPLC) method is presented for measuring of quinapril in tablets, using a reversed-phase technique and UV detection at 211 nm. The isocratic elution was used to quantify the analyte and the internal standard-perindopril. The samples were chromatographed on LiChrosorb RP-18 column and the mobile phase was phosphate buffer pH 2.5-acetonitrile (6:4, v/v). The method was linear between 0.1–0.5 mg ml−1. Over the tested concentration range the intra-day coefficient of variation for replicate analyses in tablets ranged from 0.88 to 2.70%. The detection limit for the analysis of quinapril was 50 μg ml−1 with 20 μl injection.

高效液相色谱法测定喹奈普利片剂中的含量
建立了一种简便、准确的高效液相色谱法(HPLC),采用反相技术和21nm紫外检测技术测定奎普利片中奎普利的含量。采用等密度洗脱法定量分析物和内标培哚普利。色谱柱为LiChrosorb RP-18,流动相为磷酸缓冲液pH 2.5-乙腈(6:4,v/v)。方法在0.1 ~ 0.5 mg ml−1之间呈线性关系。在测试浓度范围内,片剂重复分析的日内变异系数为0.88 ~ 2.70%。喹奈普利的检出限为50 μ ml−1,注射20 μl。
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