Quantitative analysis of polymorphic mixtures of ranitidine hydrochloride by Raman spectroscopy and principal components analysis

被引:79
作者
Pratiwi, D
Fawcett, JP
Gordon, KC
Rades, T
机构
[1] Univ Otago, Sch Pharm, Solid State Res Grp, Dunedin, New Zealand
[2] Univ Otago, Dept Chem, Dunedin, New Zealand
关键词
ranitidine-HCl; polymorphism; Raman spectroscopy; principal components analysis; quantitative analysis;
D O I
10.1016/S0939-6411(02)00113-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ranitidine hydrochloride exists as two polymorphs, forms I and II, both of which are used to manufacture commercial tablets. Raman spectroscopy can be used to differentiate the two forms but univariate methods of quantitative analysis of one polymorph as an impurity in the other lack sensitivity. We have applied principal components analysis (PCA) of Raman spectra to binary mixtures of the two polymorphs and to binary mixtures prepared by adding one polymorph to powdered tablets of the other. Based on absorption measurements of seven spectral regions, it was found that >97% of the spectral variation was accounted for by three principal components. Quantitative calibration models generated by multiple linear regression predicted a detection limit and quantitation limit for either forms I or II in mixtures of the two of 0.6 and 1.8%, respectively. This study demonstrates that PCA of Raman spectroscopic data provides a sensitive method for the quantitative analysis of polymorphic impurities of drugs in commercial tablets with a quantitation limit of less than 2%. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:337 / 341
页数:5
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