Cullen Edward, Liao James, Lukacsko Peter, Niecestro Robert, Friedhoff Lawrence
Andrx Laboratories, Hackensack, NJ 07601, USA.
Biopharm Drug Dispos. 2004 Sep;25(6):261-3. doi: 10.1002/bdd.407.
The pharmacokinetics and dose-exposure relationship of an extended-release formulation of metformin (ER-metformin) was investigated in a randomized, single-dose, four-period crossover study in 24 healthy male volunteers. During each study period, subjects received a randomly assigned dose containing 1000, 1500, 2000 or 2500 mg metformin. Blood samples were drawn 0-72 h after dosing for pharmacokinetic and dose-proportionality assessment. Although several pairwise comparisons between dose groups were significant (p<0.05) with respect to dose-normalized C(max), AUC(0-72 h), and AUC( infinity ), the magnitude of the difference across the dose range was <20% for AUC(0-72 h) and AUC( infinity ), and was < or = 30% for C(max). The results indicate a consistent and predictable increase in metformin exposure with an extended-release formulation of metformin over 1000 to 2500 mg.
在一项针对24名健康男性志愿者的随机、单剂量、四周期交叉研究中,对二甲双胍缓释制剂(ER-二甲双胍)的药代动力学和剂量-暴露关系进行了研究。在每个研究周期内,受试者接受随机分配的含1000、1500、2000或2500毫克二甲双胍的剂量。给药后0至72小时采集血样,用于药代动力学和剂量比例评估。尽管剂量组之间在剂量标准化的C(max)、AUC(0-72 h)和AUC( infinity )方面的几个两两比较具有显著性(p<0.05),但对于AUC(0-72 h)和AUC( infinity ),整个剂量范围内差异的幅度<20%,对于C(max),差异幅度<或 = 30%。结果表明,二甲双胍缓释制剂在1000至2500毫克范围内,二甲双胍的暴露量呈一致且可预测的增加。