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反相高效液相色谱-紫外检测法测定人血浆中尼可地尔的灵敏方法。

Sensitive method for determination of nicorandil in human plasma by reversed-phase high-performance liquid chromatography with ultraviolet detection.

作者信息

Tanikawa M, Uzu M, Ohsawa Y, Fukushima M

机构信息

Assay Technology Laboratory, Development and Technology Division, Chugai Phamaceutical Co. Ltd., Tokyo, Japan.

出版信息

J Chromatogr. 1993 Jul 23;617(1):163-7. doi: 10.1016/0378-4347(93)80437-9.

DOI:10.1016/0378-4347(93)80437-9
PMID:8376532
Abstract

A sensitive method for the determination of nicorandil, an anti-anginal drug, has been developed. The method involves solid-phase extraction of the drug and an internal standard using a Bond-Elut PH extraction column, liquid-liquid extraction with methyl acetate and dichloromethane, and reversed-phase high-performance liquid chromatography on a mu Bondapak C18 column with an ultraviolet detector. The limit of determination in plasma was 3 ng/ml and the intra-day coefficient of variation (n = 7) was less than 10%.

摘要

已开发出一种用于测定抗心绞痛药物尼可地尔的灵敏方法。该方法包括使用Bond-Elut PH萃取柱对药物和内标进行固相萃取,用乙酸甲酯和二氯甲烷进行液-液萃取,以及在配有紫外检测器的μ Bondapak C18柱上进行反相高效液相色谱分析。血浆中的测定限为3 ng/ml,日内变异系数(n = 7)小于10%。

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Selective and validated spectrophotometric methods for the determination of nicorandil in pharmaceutical formulations.用于测定药物制剂中尼可地尔的选择性及经过验证的分光光度法。
AAPS J. 2004 Nov 30;6(4):e34. doi: 10.1208/aapsj060434.