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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >IMPLICATIONS OF MOBILE PHASE COMPOSITION AND PH ON THE CHROMATOGRAPHIC SEPARATION OF AMITRIPTYLINE AND ITS METABOLITE NORTRIPTYLINE
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IMPLICATIONS OF MOBILE PHASE COMPOSITION AND PH ON THE CHROMATOGRAPHIC SEPARATION OF AMITRIPTYLINE AND ITS METABOLITE NORTRIPTYLINE

机译:流动相组成和PH值对阿米替林及其代谢型去甲三氮灵色谱分离的影响

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Objective: Separation of tricyclic compounds sets the keystone for determining parent drug to metabolite concentration ratios and analysing impurities. The combined effects of acetonitrile composition and pH of the mobile phase on the separation of amitriptyline and nortriptyline by reversed-phase high-performance liquid chromatography (RP-HPLC) are presented. Methods: A series of RP-HPLC triplicate runs were carried out using acetonitrile and a phosphate buffer as the mobile phase and a Kinetex ? C18 LC Column as the stationary phase using an Agilent 1260 Infinity Series ? II liquid chromatography system with UV/visible detection. The stationary phase, column temperature, injection volume and flow rate were kept unchanged during analysis. Mobile phase composition and pH were varied to observe impact on peak shape, resolution and retention time, taking into consideration green analytical chemistry aspects. Results: Optimal chromatographic outcomes were achieved when using the mobile phase made up of 35% acetonitrile and 65% buffer at a pH of 5.6. These conditions resulted in nortriptyline and amitriptyline eluting at 4.66 min and 5.92 min respectively. Increasing the organic modifier content of the mobile phase to 40% completed separation within a run time of 4 min with comparable resolution. The 2 min gained by increasing 5% acetonitrile may not be justified due to potential implications on greening laboratory practices. Conclusion: Reversed-phase chromatography embodies a simple method for the separation of compounds that are similar in structure. Attuning the percentage of organic modifier and buffer pH provides acceptable retention times, without compromising resolution between neighbouring peaks.
机译:目的:三环化合物的分离为确定母体药物与代谢物的浓度比和分析杂质奠定了基石。提出了乙腈组成和流动相pH对反相高效液相色谱(RP-HPLC)分离阿米替林和去甲替林的综合影响。方法:使用乙腈和磷酸盐缓冲液作为流动相,并使用Kinetex?进行了一系列RP-HPLC三次重复实验。使用Agilent 1260 Infinity系列作为固定相的C18液相色谱柱II具有UV /可见光检测的液相色谱系统。在分析过程中,固定相,色谱柱温度,进样量和流速均保持不变。考虑到绿色分析化学方面的变化,可以改变流动相的组成和pH值,以观察对峰形,分离度和保留时间的影响。结果:当使用由35%的乙腈和65%的缓冲液(pH值为5.6)组成的流动相时,可获得最佳的色谱结果。这些条件导致去甲替林和阿米替林分别在4.66分钟和5.92分钟洗脱。在4分钟的运行时间内,将流动相中有机改性剂的含量提高至40%,可以完成分离,并且具有相当的分离度。由于对绿化实验室操作有潜在影响,因此增加5%乙腈获得的2分钟时间可能不合理。结论:反相色谱法是一种分离结构相似化合物的简单方法。调节有机改性剂和缓冲液pH的百分比可提供可接受的保留时间,而不会影响相邻峰之间的分离度。

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