Quantification of flupirtine maleate polymorphs using X-ray powder diffraction

被引:0
|
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
相关论文
共 50 条
  • [41] Evaluation of the detectability and quantification of respirable crystalline silica by X-ray powder diffraction methods
    Smith, DK
    POWDER DIFFRACTION, 1997, 12 (04) : 200 - 227
  • [42] Femtosecond x-ray powder diffraction on KDP
    Zamponi, F.
    Rothhardt, P.
    Stingl, J.
    Woerner, M.
    Elsaesser, T.
    2011 CONFERENCE ON LASERS AND ELECTRO-OPTICS (CLEO), 2011,
  • [43] Standardisation of X-ray powder diffraction methods
    Berti, G
    Delhez, R
    Norval, S
    Peplinski, B
    Tolle, E
    Verollet, J
    EUROPEAN POWDER DIFFRACTION EPDIC 8, 2004, 443-4 : 31 - 34
  • [44] X-RAY DIFFRACTION POWDER DATA FOR THE STEROIDS
    BEHER, WT
    PARSONS, J
    BAKER, GD
    ANALYTICAL CHEMISTRY, 1955, 27 (10) : 1569 - 1573
  • [45] REVISED X-RAY POWDER DIFFRACTION TECHNIQUE
    JOHNSON, GG
    INDUSTRIAL AND ENGINEERING CHEMISTRY, 1969, 61 (05): : 79 - &
  • [46] X-ray powder diffraction data for norandrostenedione
    Tang, Pei Xiao
    Wu, Xiao Qing
    Pan, Qing Qing
    Zhang, Li Li
    Cheng, Qiang
    Li, Hui
    POWDER DIFFRACTION, 2013, 28 (04) : 302 - 304
  • [47] X-ray Powder Diffraction Characterization of Pyrope
    王冠鑫
    龚国洪
    Chinese Journal of Geochemistry(English Language Edition), 1990, (03) : 284 - 288
  • [48] X-ray Powder Diffraction Characterization of Nanoparticles
    Giannini, Cinzia
    Guagliardi, Antonietta
    Zanchet, Daniela
    Cervellino, Antonio
    Ladisa, Massimo
    ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2005, 61 : C405 - C405
  • [49] STEROID X-RAY DIFFRACTION POWDER DATA
    PARSONS, J
    BEHER, WT
    BAKER, GD
    ANALYTICAL CHEMISTRY, 1956, 28 (10) : 1514 - 1518
  • [50] X-ray powder diffraction simulation with a microcomputer
    Masson, BL
    JOURNAL OF CHEMICAL EDUCATION, 1996, 73 (10) : 918 - 921