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人血浆中瑞格列奈HPLC法测定及其药代动力学研究[J]. 中国药科大学学报, 2001, (1): 32-35.
引用本文: 人血浆中瑞格列奈HPLC法测定及其药代动力学研究[J]. 中国药科大学学报, 2001, (1): 32-35.
Determination ofRepaglinide in Plasma by HPLC and Its Pharmacokinetics in Men[J]. Journal of China Pharmaceutical University, 2001, (1): 32-35.
Citation: Determination ofRepaglinide in Plasma by HPLC and Its Pharmacokinetics in Men[J]. Journal of China Pharmaceutical University, 2001, (1): 32-35.

人血浆中瑞格列奈HPLC法测定及其药代动力学研究

Determination ofRepaglinide in Plasma by HPLC and Its Pharmacokinetics in Men

  • 摘要: 目的建立了人血浆中瑞格列奈浓度的HPLC测定方法,研究瑞格列奈在人体中药物动力学行为。方法血浆样品经酸化后,用醋酸乙酯提取,色谱柱为C18Shim-packCLC-ODS,流动相为0.10mol/L柠檬酸-醋酸钠缓冲液(pH4.0)-甲醇(27∶73)(v/v)。紫外检测波长243nm。测定了22名受试者单剂量口服瑞格列奈4mg后血药浓度-时间过程。结果最低检测浓度2.5ng/ml,回收率大于90%,日间和日内的变异系数小于15%,线性范围为2.5~100.0ng/ml,符合生物样品分析的要求。受试者口服瑞格列奈片4mg后,估算的末端相半衰期0.83±0.31h,峰时间0.75±0.41h,峰浓度53.32±24.94ng/ml,MRT1.58±0.41h,AUC4074.95±30.57ng

     

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