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高效液相色谱-安培检测法定量测定药物和尿液中的血管紧张素转换酶抑制剂西拉普利及其活性代谢物西拉普利拉。

Quantitative determination of the angiotensin-converting enzyme inhibitor cilazapril and its active metabolite cilazaprilat in pharmaceuticals and urine by high-performance liquid chromatography with amperometric detection.

作者信息

Prieto J A, Jiménez R M, Alonso R M

机构信息

Departamento de Química Analítica, Facultad de Ciencias, Universidad del País Vasco, Bilbao, Spain.

出版信息

J Chromatogr B Biomed Sci Appl. 1998 Sep 4;714(2):285-92. doi: 10.1016/s0378-4347(98)00226-6.

Abstract

A rapid and simple high-performance liquid chromatographic method with amperometric detection has been developed for the quantitation of cilazapril and its active metabolite and degradation product cilazaprilat in urine and tablets. The chromatographic system consisted of a microBondapak C18 column, using a mixture of methanol-5 mM phosphoric acid (50:50, v/v) as mobile phase, which was pumped at a flow-rate of 1.0 ml/min. The column was kept at a constant temperature of (40+/-0.2) degrees C. Detection was performed using a glassy carbon electrode at a potential of 1350 mV. Sample preparation for urine consisted of a solid-phase extraction using C8 cartridges. This procedure allowed recoveries greater than 85% for both compounds. The method proved to be accurate, precise and sensitive enough to be applied to pharmacokinetic studies and it has been applied to urine samples obtained from four hypertensive patients (detection limit of 50 ng/ml for cilazapril and 40 ng/ml for cilazaprilat in urine). Results were in good agreement with pharmacokinetic data.

摘要

已开发出一种快速简便的高效液相色谱-安培检测法,用于定量测定尿液和片剂中的西拉普利及其活性代谢物和降解产物西拉普利拉。色谱系统由一根微Bondapak C18柱组成,以甲醇-5 mM磷酸(50:50,v/v)的混合物作为流动相,流速为1.0 ml/min。柱温保持在(40±0.2)℃恒定。使用玻碳电极在1350 mV的电位下进行检测。尿液的样品制备包括使用C8柱进行固相萃取。该方法对两种化合物的回收率均大于85%。该方法经证明准确、精密且灵敏,足以应用于药代动力学研究,并且已应用于从四名高血压患者获得的尿液样本(尿液中西拉普利的检测限为50 ng/ml,西拉普利拉的检测限为40 ng/ml)。结果与药代动力学数据高度一致。

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