Liquid chromatography-tandem mass spectrometric assay for the light sensitive calcium channel antagonist lacidipine in human plasma

被引:6
|
作者
Karra, Vijaya Kumari [2 ]
Pilli, Nageswara Rao [2 ]
Polagani, Srinivasa Rao [3 ]
Inamadugu, Jaswanth Kumar [4 ]
Rao, J. V. L. N. Seshagiri [1 ]
机构
[1] Andhra Univ, Univ Coll Pharmaceut Sci, Visakhapatnam 530003, Andhra Pradesh, India
[2] Jawaharlal Nehru Technol Univ, Univ Coll Pharmaceut Sci, Hyderabad 500085, Andhra Pradesh, India
[3] Rayalaseema Univ, Kurnool 518002, India
[4] Sri Venkateswara Univ, Analyt & Environm Chem Div, Tirupati 517502, India
关键词
Lacidipine in human plasma; Solid-phase extraction (SPE); Liquid chromatography-tandem mass spectrometry; Method validation; Pharmacokinetic studies; HYPERTENSION; 1,4-DIHYDROPYRIDINES;
D O I
10.1016/j.jpba.2012.02.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel, rapid and sensitive liquid chromatography/tandem mass spectrometry method was developed and validated for the quantification of calcium channel antagonist lacidipine in human plasma. Carbamazepine was used as an internal standard. Analyte and the internal standard were extracted from human plasma by solid-phase extraction technique. The reconstituted samples were chromatographed on a C-18 column by using a mixture of acetonitrile-ammonium acetate buffer (5 mM) (80:20, v/v) as the mobile phase at a flow rate of 1.0 mL/min. The calibration curve obtained was linear (r(2) >= 0.9990) over the concentration range of 0.05-12.5 ng/mL. The multiple reaction-monitoring mode was used for quantification of ion transitions at m/z 456.2/354.2 and 237.1/194.1 for the drug and the internal standard, respectively. The results of the intra- and inter-day precision and accuracy studies were well within the acceptable limits. A run time of 2.2 min for each sample made it possible to analyze more than 300 plasma samples per day. The proposed method was found to be applicable to clinical studies. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 217
页数:7
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