Polagani Srinivasa Rao, Pilli Nageswara Rao, Gajula Ramakrishna, Gandu Venkateswarlu
Research Studies, Rayalaseema University, Kurnool 518002, India.
Wellquest Clinical Research, Ramanthapur, Hyderabad 500013, India.
J Pharm Anal. 2013 Feb;3(1):9-19. doi: 10.1016/j.jpha.2012.09.002. Epub 2012 Oct 3.
A simple, rapid and sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) assay method has been developed and fully validated for the simultaneous quantification of atorvastatin, metformin and glimepiride in human plasma. Carbamazepine was used as internal standard (IS). The analytes were extracted from 200 μL aliquots of human plasma via protein precipitation using acetonitrile. The reconstituted samples were chromatographed on a Alltima HP C18 column by using a 60:40 (v/v) mixture of acetonitrile and 10 mM ammonium acetate (pH 3.0) as the mobile phase at a flow rate of 1.1 mL/min. The calibration curves obtained were linear ( ≥0.99) over the concentration range of 0.50-150.03 ng/mL for atorvastatin, 12.14-1207.50 ng/mL for metformin and 4.98-494.29 ng/mL for glimepiride. The API-4000 LC-MS/MS in multiple reaction monitoring (MRM) mode was used for detection. The results of the intra- and inter-day precision and accuracy studies were well within the acceptable limits. All the analytes were found to be stable in a battery of stability studies. The method is precise and sensitive enough for its intended purpose. A run time of 2.5 min for each sample made it possible to analyze more than 300 plasma samples per day. The developed assay method was successfully applied to a pharmacokinetic study in human male volunteers.
已开发并完全验证了一种简单、快速且灵敏的液相色谱-串联质谱(LC-MS/MS)分析方法,用于同时定量测定人血浆中的阿托伐他汀、二甲双胍和格列美脲。卡马西平用作内标(IS)。通过用乙腈进行蛋白沉淀,从200μL人血浆等分试样中提取分析物。将重构后的样品在Alltima HP C18柱上进行色谱分析,使用乙腈和10 mM醋酸铵(pH 3.0)的60:40(v/v)混合物作为流动相,流速为1.1 mL/min。获得的校准曲线在阿托伐他汀浓度范围为0.50 - 150.03 ng/mL、二甲双胍浓度范围为12.14 - 1207.50 ng/mL、格列美脲浓度范围为4.98 - 494.29 ng/mL内呈线性(≥0.99)。使用处于多反应监测(MRM)模式的API-4000 LC-MS/MS进行检测。日内和日间精密度及准确度研究结果均在可接受范围内。在一系列稳定性研究中发现所有分析物均稳定。该方法对于其预期目的而言足够精确和灵敏。每个样品的运行时间为2.5分钟,使得每天能够分析300多个血浆样品。所开发的分析方法已成功应用于男性志愿者的药代动力学研究。