Trone Mark D, Vaughn Michael S, Cole Steven R
Chemical Development, GlaxoSmithKline, 5 Moore Dr., Research Triangle Park, NC 27709, USA.
J Chromatogr A. 2006 Nov 10;1133(1-2):104-11. doi: 10.1016/j.chroma.2006.08.003. Epub 2006 Aug 24.
A peak trapping recycle chromatography system has been developed and optimized for peak purity assessment of active pharmaceutical ingredients analyzed by high performance liquid chromatography (HPLC). After being analyzed using a reversed phase analytical column, peaks of interest are trapped and are subsequently introduced to a recycle chromatography system. In addition to the increased effective length afforded the recycling system, the small selectivity difference between the analytical and recycling methods help separate potential impurities under the main peak. For more difficult to separate components, the increased efficiency of recycle chromatography provides the necessary resolution. Over 227,000 theoretical plates have been obtained in the recycle dimension for some compounds. The sensitivity of the system fell short of the target (0.1%), but it did show sensitivity (0.5%) comparable to other peak purity techniques commonly used in the pharmaceutical industry. The recovery and repeatability have also been shown to be adequate for peak purity assessment. The system has also been automated using a Visual Basic macro, simplifying the interface allowing it to be used as an open access instrument.
已开发并优化了一种峰捕集循环色谱系统,用于通过高效液相色谱(HPLC)分析的活性药物成分的峰纯度评估。使用反相分析柱进行分析后,感兴趣的峰被捕集,随后引入循环色谱系统。除了循环系统提供的有效长度增加外,分析方法和循环方法之间较小的选择性差异有助于分离主峰下的潜在杂质。对于更难分离的组分,循环色谱效率的提高提供了必要的分离度。对于某些化合物,在循环维度上已获得超过227,000个理论塔板数。该系统的灵敏度未达到目标(0.1%),但确实显示出与制药行业常用的其他峰纯度技术相当的灵敏度(0.5%)。回收率和重复性也已证明足以进行峰纯度评估。该系统还使用Visual Basic宏实现了自动化,简化了界面,使其可作为开放获取仪器使用。