Yardımcı Ceren, Ozaltın Nuran, Gürlek Alper
Department of Analytical Chemistry, Faculty of Pharmacy, Hacettepe University, 06100 Sihhiye, Ankara, Turkey.
Talanta. 2007 Jun 15;72(4):1416-22. doi: 10.1016/j.talanta.2007.01.042. Epub 2007 Jan 30.
A novel, fast and simple liquid chromatographic method was developed and validated for the simultaneous determination of rosiglitazone and metformin in human plasma. The analysis was performed on a phenyl column (250mmx4.6mm i.d., 5mum) using a gradient method starting with mobile phase composed of acetonitrile:5mM acetate buffer pH 5.5 (75:25, v/v). The flow rate was 1mLmin(-1). UV detection was performed at 245nm and verapamil was used as internal standard. The total run time was less than 10min. Sample preparation included a simple protein precipitation step with acetonitrile. Validation experiments were performed to demonstrate stability, specificity, sensitivity, linearity, accuracy, precision and robustness. The limit of quantification was 100ngmL(-1) for rosiglitazone and 250ngmL(-1) for metformin. The extraction recoveries were 100.02-105.0% for rosiglitazone and 105.64-103.88% for metformin. The method was applied with success to plasma samples obtained from diabetic patients undergoing treatment with rosiglitazone and metformin.
建立并验证了一种新颖、快速且简便的液相色谱法,用于同时测定人血浆中的罗格列酮和二甲双胍。分析在苯基柱(250mm×4.6mm内径,5μm)上进行,采用梯度洗脱法,起始流动相为乙腈:5mM醋酸盐缓冲液pH 5.5(75:25,v/v)。流速为1mLmin(-1)。在245nm处进行紫外检测,维拉帕米用作内标。总运行时间少于10分钟。样品制备包括用乙腈进行简单的蛋白沉淀步骤。进行了验证实验以证明稳定性、特异性、灵敏度、线性、准确度、精密度和稳健性。罗格列酮的定量限为100ngmL(-1),二甲双胍的定量限为250ngmL(-1)。罗格列酮的提取回收率为100.02 - 105.0%,二甲双胍的提取回收率为105.64 - 103.88%。该方法成功应用于从接受罗格列酮和二甲双胍治疗的糖尿病患者获取的血浆样本。