Li Wei, Hu Chang-qin
National Institute for the Control of Pharmaceutical and Biological Products, Beijing 100050, China.
J Chromatogr A. 2008 May 9;1190(1-2):141-9. doi: 10.1016/j.chroma.2008.02.097. Epub 2008 Mar 6.
A novel qualitative analytical method for peak tracking in impurity profiling control by the correlation of spectra was established. Two-dimensional (2D) standard spectrochromatographic data produced by high-performance liquid chromatography with diode array detection (HPLC-DAD) were compared with sample data to develop two-dimensional chromatographic spectral correlative maps. Taking full advantage of separation efficiency of HPLC and spectral specificity of the analytes, the method was successfully used to recognize impurities in quinolone antibacterials, when in combination with relative retention times (RRTs). For the comparison of spectra was expanded to three-dimensional space, simultaneous identification of the chromatographic peaks can be obtained rapidly without preparation and injection of a reference solution, even when the mobile phase changed or the peaks of multi-component samples overlapped.
建立了一种通过光谱相关性进行杂质谱控制中峰跟踪的新型定性分析方法。将高效液相色谱-二极管阵列检测(HPLC-DAD)产生的二维(2D)标准光谱色谱数据与样品数据进行比较,以生成二维色谱光谱相关图。该方法充分利用了HPLC的分离效率和分析物的光谱特异性,与相对保留时间(RRT)结合时,成功用于识别喹诺酮类抗菌药物中的杂质。由于光谱比较扩展到三维空间,即使流动相发生变化或多组分样品的峰重叠,也无需制备和进样参考溶液即可快速同时识别色谱峰。