School of Pharmaceutical Sciences, University of Science Malaysia, Penang.
J Chromatogr B Biomed Sci Appl. 1998 Jun 12;710(1-2):243-6. doi: 10.1016/s0378-4347(98)00117-0.
A simple high-performance liquid chromatographic method using ultraviolet detection was developed for the determination of metformin in human plasma. The method entailed direct injection of the plasma sample after deproteination using perchloric acid. The mobile phase comprised 0.01 M potassium dihydrogen orthophosphate (pH 3.5) and acetonitrile (60:40, v/v). Analyses were run at a flow-rate of 1.0 ml/min with the detector operating at a detection wavelength of 234 nm. The method is specific and sensitive, with a quantification limit of approximately 60 ng/ml and a detection limit of 15 ng/ml at a signal-to-noise ratio of 3:1. The mean absolute recovery value was about 97%, while the within-day and between-day coefficient of variation and percent error values of the assay method were all less than 8%. The calibration curve was linear over a concentration range of 62.5-4000 ng/ml.
建立了一种采用紫外检测的简单高效液相色谱法,用于测定人血浆中的二甲双胍。该方法包括用高氯酸脱蛋白后直接进样血浆样品。流动相由0.01 M磷酸二氢钾(pH 3.5)和乙腈(60:40,v/v)组成。分析以1.0 ml/min的流速进行,检测器在234 nm的检测波长下运行。该方法具有特异性和灵敏性,定量限约为60 ng/ml,在信噪比为3:1时检测限为15 ng/ml。平均绝对回收率约为97%,而该测定方法的日内和日间变异系数及误差百分比值均小于8%。校准曲线在62.5 - 4000 ng/ml的浓度范围内呈线性。