Thoma K, Ziegler I
Institute for Pharmacy and Food Chemistry, Munich, Germany.
Eur J Pharm Biopharm. 1998 Sep;46(2):183-90. doi: 10.1016/s0939-6411(97)00160-4.
A HPLC-method was developed to determine both fenoldopam, a weakly basic drug and succinic acid, a pH-adjuster for this drug in dissolution media. The usual assays for succinic acid were not applicable due to its low UV-absorption, the low pH-value of samples or the presence of buffer salts and fenoldopam. The described method is a simple non-ion-pair reversed phase HPLC-method using a fast scanning UV-detector and a PC software program for the quantification of both components. Succinic acid is detected at 205 nm and fenoldopam at 225 nm. The UV-spectrum is used to determine peak purity and to identify peaks (carried out at a 99.9% match). This is especially important as in some of the investigated samples an unknown peak elutes immediately after succinic acid, resulting in spurious high contents, if mistaken for succinic acid. The simple method accomplished the simultaneous quantification of both, succinic acid and fenoldopam, by an accurate, precise, specific and reproducible assay, with a linear range covering all concentrations relevant for dissolution testing. The method is stability indicating and can also be used for the quantification of fumaric acid, another pH-adjuster in dissolution media together with fenoldopam.
开发了一种高效液相色谱法(HPLC),用于测定弱碱性药物非诺多泮以及该药物在溶出介质中的pH调节剂琥珀酸。由于琥珀酸的紫外吸收低、样品pH值低或存在缓冲盐和非诺多泮,常规的琥珀酸测定方法不适用。所描述的方法是一种简单的非离子对反相高效液相色谱法,使用快速扫描紫外检测器和PC软件程序对两种成分进行定量。琥珀酸在205nm处检测,非诺多泮在225nm处检测。紫外光谱用于确定峰纯度和识别峰(匹配度为99.9%)。这一点尤为重要,因为在一些研究样品中,一个未知峰紧跟在琥珀酸之后洗脱,如果误认该未知峰为琥珀酸,会导致含量虚高。该简单方法通过准确、精密、特异且可重现的分析,实现了琥珀酸和非诺多泮的同时定量,线性范围涵盖了溶出度测试的所有相关浓度。该方法具有稳定性指示作用,还可用于定量溶出介质中与非诺多泮一起使用的另一种pH调节剂富马酸。