HPLC method for determination of verapamil in human plasma after solid-phase extraction

Violeta Ivanova , Dragica Zendelovska , Marina Stefova , Trajče Stafilov
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引用次数: 27

Abstract

A simple, rapid and precise HPLC method has been developed for the assay of verapamil in human plasma. The clean up of the plasma samples was tested using several adsorbents for solid-phase extraction and best recovery was obtained using mixed-mode cartridges (HLB - hydrophilic-lipophilic balance) ranging between 94.70 and 103.71%. HPLC separation was performed with isocratic elution on Lichrospher 60 RP-select B column (250 mm × 4 mm I.D., 5 μm particle size). The mobile phase was 40% acetonitrile and 0.025 mol/L KH2PO4 with pH 2.5 at flow rate of 1 mL/min. Diltiazem was used as internal standard and the detection wavelength was 200 nm. The calibration curves were linear in the range of 10–500 ng/mL. The developed method is convenient for routine analysis of verapamil in human plasma.

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固相萃取法测定人血浆中维拉帕米含量
建立了一种简便、快速、精确的测定人血浆中维拉帕米含量的高效液相色谱方法。采用多种吸附剂对血浆样品进行固相萃取,回收率最高的是混合模式(HLB -亲水-亲脂平衡),回收率在94.70 ~ 103.71%之间。色谱柱为Lichrospher 60 RP-select B (250 mm × 4 mm内径,5 μm粒径),采用等压洗脱。流动相为40%乙腈和0.025 mol/L KH2PO4, pH为2.5,流速为1 mL/min。以地尔硫卓为内标,检测波长为200 nm。在10 ~ 500 ng/mL范围内,标定曲线呈线性关系。该方法便于人血浆中维拉帕米的常规分析。
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