DSC, X-ray and FTIR studies of a gemfibrozil/dimethyl-β-cyclodextrin inclusion complex produced by co-grinding

被引:64
作者
Aigner, Z. [1 ]
Berkesi, O. [2 ]
Farkas, G. [1 ]
Szabo-Revesz, P. [1 ]
机构
[1] Univ Szeged, Fac Pharm, Dept Pharmaceut Technol, H-6720 Szeged, Hungary
[2] Univ Szeged, Fac Sci & Informat, Dept Phys Chem & Mat Sci, H-6720 Szeged, Hungary
关键词
Gemfibrozil; Dimethyl-beta-cyclodextrin; DSC; XRPD; FTIR with curve-fitting analysis;
D O I
10.1016/j.jpba.2011.08.034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The steps of formation of an inclusion complex produced by the co-grinding of gemfibrozil and dimethyl-beta-cyclodextrin were investigated by differential scanning calorimetry (DSC), X-ray powder diffractometry (XRPD) and Fourier transform infrared (FTIR) spectroscopy with curve-fitting analysis. The endothermic peak at 59.25 degrees C reflecting the melting of gemfibrozil progressively disappeared from the DSC curves of the products on increase of the duration of co-grinding. The crystallinity of the samples too gradually decreased, and after 35 min of co-grinding the product was totally amorphous. Up to this co-grinding time. XRPD and FTIR investigations indicated a linear correlation between the cyclodextrin complexation and the co-grinding time. After co-grinding for 30 min, the ratio of complex formation did not increase. These studies demonstrated that co-grinding is a suitable method for the complexation of gemfibrozil with dimethyl-beta-cyclodextrin. XRPD analysis revealed the amorphous state of the gemfibrozil-dimethyl-beta-cyclodextrin product. FTIR spectroscopy with curve-fitting analysis may be useful as a semiquantitative analytical method for discriminating the molecular and amorphous states of gemfibrozil. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 67
页数:6
相关论文
共 18 条
[1]   Thermoanalytical, FTIR and X-ray studies of gemfibrozil-cyclodextrin complexes [J].
Aigner, Z ;
Hassan, HB ;
Berkesi, O ;
Kata, M ;
Eros, I .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2005, 81 (02) :267-272
[2]   Investigation of the triamterene-beta-cyclodextrin system prepared by co-grinding [J].
Arias, MJ ;
Moyano, JR ;
Gines, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 153 (02) :181-189
[3]   Optimisation of spray-drying process variables for dry powder inhalation (DPI) formulations of corticosteroid/cyclodextrin inclusion complexes [J].
Cabral-Marques, Helena ;
Almeida, Rita .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 73 (01) :121-129
[4]   Solid-state characterization of glyburide-cyclodextrin co-ground products [J].
Cirri, M ;
Maestrelli, F ;
Furlanetto, S ;
Mura, P .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2004, 77 (02) :413-422
[5]  
Fromming KH., 1994, CYCLODEXTRINS PHARM
[6]  
HASSAN HB, 2004, J INCL PHENOM MACRO, V50, P219, DOI DOI 10.1007/S10847-004-3124-7
[7]  
*MEDIMEDIA INF KFT, 2002, GYOG KOMP 2002, P713
[8]  
*MERCK CO INC, 1989, MERCK IND, P686
[9]  
Patil JS., 2010, Int J Pharm Sci Rev Res, V2, P29, DOI DOI 10.1136/BMJ333.7574.873-A
[10]  
QIFANG W, 2010, ASIAN J PHARM SCI, V5, P185