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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Comprehensive two-dimensional liquid chromatography separations of pharmaceutical samples using dual Fused-Core columns in the 2nd dimension
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Comprehensive two-dimensional liquid chromatography separations of pharmaceutical samples using dual Fused-Core columns in the 2nd dimension

机译:使用二维双熔融核色谱柱对药物样品进行全面的二维液相色谱分离

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摘要

This paper focuses on the application of RPLC x RPLC to pharmaceutical analysis and addresses the specific problem of separating co-eluting impurities/degradation products that maybe "hidden" within the peak envelope of the active pharmaceutical ingredient (API) and thus may escape detection by conventional methods. A comprehensive two-dimensional liquid chromatograph (LC x LC) was constructed from commercially available HPLC equipment. This system utilizes two independently configurable 2nd dimension binary pumping systems to deliver independent flow rates, gradient profiles and mobile phase compositions to dual Fused-Core secondary columns. Very fast gradient separations (30 s total cycle time) were achieved at ambient temperature without excessive backpressure and without compromising optimal 1st dimension sampling rates. The operation of the interface is demonstrated for the analysis of a 1 mg/ml standard mixture containing 0.05% of a minor component. The practicality of using RPLC x RPLC for the analysis of actual co-eluting pharmaceutical degradation products, by exploiting pH-induced changes in selectivity, is also demonstrated using a three component mixture. This mixture (an API, an oxidation product of the API at 1.0%, w/w, and a photo degradant of the API at 0.5%. w/w) was used to assess the stability indicating nature of an established LC method for analysis of the API. (C) 2008 Elsevier B.V. All rights reserved.
机译:本文着重介绍RPLC x RPLC在药物分析中的应用,并解决了分离共洗脱杂质/降解产物的特定问题,这些杂质/降解产物可能“隐藏”在活性药物成分(API)的峰包络内,因此可能无法通过检测常规方法。使用市售的HPLC设备构建全面的二维液相色谱仪(LC x LC)。该系统利用两个可独立配置的二维二元泵送系统,将独立的流速,梯度分布和流动相组成传递给双熔融核二级色谱柱。在环境温度下,可以实现非常快速的梯度分离(总循环时间为30 s),而不会产生过多的背压,也不会影响最佳的一维采样率。该界面的操作可用于分析含有0.05%微量成分的1 mg / ml标准混合物。还通过使用三组分混合物证明了通过利用pH诱导的选择性变化,使用RPLC x RPLC分析实际的共洗脱药物降解产物的实用性。使用该混合物(API,API的氧化产物为1.0%,w / w和API的光降解物为0.5%.w / w)评估稳定性,这表明已建立的LC分析方法的性质API。 (C)2008 Elsevier B.V.保留所有权利。

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