HPLC Determination of Metformin, Famotidine and Ranitidine by Derivatization with Benzoin from Drugs and Biological Samples

M. Alamgir, M. Y. Khuhawar, S. Memon, Amir Hayat, R. A. Zounr, Asma Chanar
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引用次数: 4

Abstract

A novel High Performance Liquid Chromatography (HPLC) method has been developed based on pre column derivatization with benzoin for determination of metformin, famotidine and ranitidine. The separation was achieved from C18 column when eluted isocratically, the solution of the drugs with methanol, water, acetonitrile and Tetra Hydrofuran (THF) (40:40:16:4 v/v) with a flow rate at 1 mL/min. UV detection was found to be 268 nm. Linear calibrations range was obtained with 2.5-12.5 μg/ml, with limits of detection (LODs) 0.091-0.30 μg/ml. The total run time for elution was 3.5 min. The derivitization, separation and quantitation was repeatable (n=4) in terms of retention time and peak height/peak area with Relative Standard Deviation (RSD) within 0.84-1.55% and 0.68-1.17% respectively. The method was applied for the analysis of metformin, famotidine and ranitidine from pharmaceutical preparations, human serum and human urine. The possible interfering effects of the sample matrix were checked by the analysis by standard addition method and matrix effect was not indicated.
高效液相色谱法测定药物和生物样品中二甲双胍、法莫替丁和雷尼替丁的含量
建立了基于柱前衍生的高效液相色谱法测定二甲双胍、法莫替丁和雷尼替丁的方法。以甲醇、水、乙腈和四氢呋喃(THF) (40:40:16:4 v/v)为溶剂,流速为1ml /min,等容洗脱,从C18柱分离。紫外检测波长为268 nm。线性校准范围为2.5 ~ 12.5 μg/ml,检出限为0.091 ~ 0.30 μg/ml。洗脱总运行时间为3.5 min。在保留时间和峰高/峰面积方面,衍生、分离和定量均可重复(n=4),相对标准偏差(RSD)分别在0.84 ~ 1.55%和0.68 ~ 1.17%之间。该方法应用于药品制剂、人血清和人尿中二甲双胍、法莫替丁和雷尼替丁的分析。采用标准加法法对样品基质可能产生的干扰效应进行了检验,未发现基质效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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