Solid State Pharmaceutical Cluster, Ireland.
J Pharm Biomed Anal. 2012 Apr 7;63:80-6. doi: 10.1016/j.jpba.2012.01.013. Epub 2012 Jan 18.
Diffraction and spectroscopic methods were evaluated for quantitative analysis of binary powder mixtures of FII(6.403) and FIII(6.525) piracetam. The two polymorphs of piracetam could be distinguished using powder X-ray diffraction (PXRD), Raman and near-infrared (NIR) spectroscopy. The results demonstrated that Raman and NIR spectroscopy are most suitable for quantitative analysis of this polymorphic mixture. When the spectra are treated with the combination of multiplicative scatter correction (MSC) and second derivative data pretreatments, the partial least squared (PLS) regression model gave a root mean square error of calibration (RMSEC) of 0.94 and 0.99%, respectively. FIII(6.525) demonstrated some preferred orientation in PXRD analysis, making PXRD the least preferred method of quantification.
衍射和光谱方法被评估用于定量分析 FII(6.403)和 FIII(6.525)吡拉西坦的二元粉末混合物。使用粉末 X 射线衍射 (PXRD)、拉曼和近红外 (NIR) 光谱可以区分吡拉西坦的两种多晶型物。结果表明,拉曼和 NIR 光谱最适合这种多晶型混合物的定量分析。当用乘法散射校正 (MSC)和二阶导数数据预处理相结合对光谱进行处理时,偏最小二乘 (PLS)回归模型分别给出了校准的均方根误差 (RMSEC)为 0.94%和 0.99%。FIII(6.525)在 PXRD 分析中表现出一些择优取向,使得 PXRD 成为最不适合定量的方法。