Quantification of flupirtine maleate polymorphs using X-ray powder diffraction

被引:0
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作者
Yu-Mei Zhao [1 ,2 ]
Zhi-Bing Zheng [1 ]
Song Li [1 ,3 ]
机构
[1] Laboratory of Computer-Aided Drug Design & Discovery,Beijing Institute of Pharmacology and Toxicology
[2] State Key Laboratory of Toxicology and Medical Countermeasures,Beijing Institute of Pharmacology and Toxicology
[3] Laboratory of Structure Identification,Beijing Institute of Pharmacology and Toxicology
关键词
Flupirtine maleate; X-ray powder diffraction; Quantitative analysis of polymorphs; Preferred orientation; Transmission;
D O I
暂无
中图分类号
TQ460.72 [];
学科分类号
100704 ;
摘要
Flupirtine maleate,a pharmaceutical compound for treating psychotic disease in clinics,has seven polymorphs.Form A,with better crystal stability and bioavailability,has been widely used as the pharmaceutical crystal form.Unfortunately,it is usually found in a polymorphic mixture with form B.In this study,pure crystal forms of A and B were prepared and characterized by X-ray powder diffraction(XRPD),Fourier transform infrared spectroscopy(FT-IR) and thermal analysis.An XRPD-based method for the quantitative determination of the amount of the flupirtine maleate polymorphs form A and form B was also established through a systematic optimization of instrumental parameters.The results of the analytical methodology validation showed that the XPRD method had a broad quantitative range of 0-100%(w/w),good linear relationship,with R~2 = 0.999,excellent repeatability and precision and low limits of detection(LoD) of 0.15%(w/w) and quantification(LoQ) of 0.5%(w/w).The results also showed that the single-peak method was not as good as the whole pattern in reducing the influence of the preferred orientation,but this can be compensated for by a systematic optimization of instrumental parameters and validating the analytical methodology to reduce errors and obtain a good,repeatable,sensitive,and accurate method.This XRPD method can be used to analyze mixtures of flupirtine maleate polymorphs(forms A and B) quantitatively and control the quality of the bulk drug.
引用
收藏
页码:1666 / 1672
页数:7
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