Development of an HPLC method for the determination of nifedipine in human plasma by solid-phase extraction

被引:31
|
作者
Zendelovska, Dragica [1 ]
Simeska, Suzana [1 ]
Sibinovska, Olgica [1 ]
Kostova, Elena [1 ]
Milosevska, Kalina [1 ]
Jakovski, Krume [1 ]
Jovanovska, Emilija [1 ]
Kikerkov, Igor [1 ]
Trojacanec, Jasmina [1 ]
Zafirov, Dimce [1 ]
机构
[1] Univ St Cyril & Methudius, Inst Preclin & Clin Pharmacol & Toxicol, Fac Med, Skopje 1000, Macedonia
关键词
nifedipine; solid-phase extraction; HPLC;
D O I
10.1016/j.jchromb.2006.03.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nifedipine, a dihydropyridine calcium channel antagonist, is widely used in the treatment of hypertension and other cardiovascular disorders. A selective, sensitive and accurate high-performance liquid chromatographic method has been developed, validated and applied for determination of nifedipine in human plasma samples. A series of studies were conducted in order to investigate the effects of mobile phase composition, buffer concentration, mobile phase pH and concentration of organic modifiers, and to develop a convenient and easy-to-use method for quantitative analysis of nifedipine. The method involves solid-phase extraction on C-18 cartridges. The chromatographic separation was accomplished on a Lichrocart Lichrospher 60 RP selectB column with a mobile phase composed of 0.020 mol/L KH2PO4 (pH 4.8) and acetonitrile (42:58, v/v). UV detection was set at 240 nm. The calibration curve was linear in the concentration range of 5.0-200.0 ng/mL for nifedipine in plasma and the. limit of quantification was 5.0 ng/mL. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 88
页数:4
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