Visky Dora, Jimidar Ilias, Van Ael Willy, Vennekens Tom, Redlich Dirk, De Smet Maurits
Johnson & Johnson Pharmaceutical Research and Development, a division of Janssen Pharmaceutica N. V., Global Analytical Department, Beerse, Belgium.
Electrophoresis. 2005 Apr;26(7-8):1541-9. doi: 10.1002/elps.200410225.
Generally reversed-phase high-performance liquid chromatography (RP-HPLC) methods are extensively applied during quality control of pharmaceutical products. Since capillary electrophoresis (CE) is based on a different separation principle and consequently results in a unique selectivity compared to RP-HPLC, it can advantageously be used as an orthogonal technique. CE equipped with a mass spectrometer detector provides even more information that can be helpful for identification and structural elucidation purposes. CE-MS was recently implemented in the method development approach to support impurity profiling of pharmaceutical products. In this paper the application of CE-electrospray ionization (ESI)-MS/MS to the impurity profiling of galantamine hydrobromide in stressed Reminyl Extended Release (ER) capsules is discussed. Reminyl ER samples were stressed at different storing conditions. The impurity profile of these samples was compared with the current RP-HPLC and chiral CE method, but also with CE-ESI-MS/MS. The combination of these three methods provided valuable data that allowed understanding comprehensively the impurity profile of these samples. Two impurities were detected at concentrations lower than 0.05%, which did not occur in nonstressed samples. Chromatographic data and the fragmentation patterns of galantamine and related compounds were also examined for identification of these two degradation products.
一般来说,反相高效液相色谱(RP-HPLC)方法在药品质量控制中被广泛应用。由于毛细管电泳(CE)基于不同的分离原理,因此与RP-HPLC相比具有独特的选择性,它可以有利地用作正交技术。配备质谱检测器的CE能提供更多有助于鉴定和结构解析的信息。CE-MS最近被应用于方法开发中,以支持药品的杂质分析。本文讨论了CE-电喷雾电离(ESI)-MS/MS在加兰他敏氢溴酸盐缓释胶囊(Reminyl ER)强制降解样品杂质分析中的应用。Reminyl ER样品在不同储存条件下进行强制降解。将这些样品的杂质谱与当前的RP-HPLC和手性CE方法进行比较,同时也与CE-ESI-MS/MS进行比较。这三种方法的结合提供了有价值的数据,有助于全面了解这些样品的杂质谱。检测到两种杂质,其浓度低于0.05%,在未强制降解的样品中未出现。还对加兰他敏及相关化合物的色谱数据和碎片模式进行了研究,以鉴定这两种降解产物。