首页> 美国卫生研究院文献>Advanced Pharmaceutical Bulletin >Enantioselective Box Behenken Optimized HPLC-DAD Method for the Simultaneous Estimation of Alogliptin Enantiomorphs in Pharmaceutical Formulations and their Pharmacokinetic Study in Rat Plasma
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Enantioselective Box Behenken Optimized HPLC-DAD Method for the Simultaneous Estimation of Alogliptin Enantiomorphs in Pharmaceutical Formulations and their Pharmacokinetic Study in Rat Plasma

机译:同时选择药物制剂中阿格列汀对映体的对映选择性盒式优化HPLC-DAD方法及其在大鼠血浆中的药代动力学研究

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摘要

>Purpose: A stereoselective high performance liquid chromatographic analytical method with photodiode array detector was developed and validated as per the International Conference on Harmonization (ICH) guidelines for the determination of alogliptin (ALO) enantiomers in formulations and rat plasma. >Methods: Enantiomeric separation was performed on a Phenomenex Lux Cellulose-2 chiral column. Box-Behnken design was used to identify the optimum conditions of the three independent variables for the desired output responses. >Results: The HPLC peaks of ALO enantiomers and the internal standard pioglitazone were achieved before 8 min with a resolution of 0.77 min between R and S enantiomer and resolution of more than 2.0 between each enantiomer and pioglitazone (internal) with more than 95% recovery. The linearity range and the limit of quantification of both the enantiomers in rat plasma were 10-70 ng mL-1 and 1.2 ng mL-1 respectively. >Conclusion: The developed method after validation was successfully applied for estimation of ALO enantiomers in formulations. Single oral dose of 25 mg of the ALO racemate tablets wereadministered to a group of 6 healthy rats for a comparative pharmacokinetic study of both theenantiomers.
机译:>目的:根据国际协调会议(ICH)指南,测定配方和大鼠血浆中阿格列汀(ALO)对映异构体,开发并验证了具有光电二极管阵列检测器的立体选择性高效液相色谱分析方法。 >方法:在Phenomenex Lux Cellulose-2手性色谱柱上进行对映体分离。 Box-Behnken设计用于确定三个独立变量针对所需输出响应的最佳条件。 >结果:ALO对映体和内标吡格列酮的HPLC峰在8 min之前达到,R和S对映体之间的分辨率为0.77 min,每种对映体与吡格列酮之间的分辨率均超过2.0(内部)回收率超过95%。大鼠血浆中两种对映体的线性范围和定量限分别为10-70 ng mL -1 和1.2 ng mL -1 。 >结论:验证后开发的方法成功地用于估计制剂中的ALO对映体。 25 mg ALO外消旋片的单次口服剂量为给予6只健康大鼠一组,以比较两种药物的药代动力学对映体。

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