Effects of Cogrinding with β-Cyclodextrin on the Solid State Fentanyl

被引:24
|
作者
Ogawa, Noriko [1 ]
Higashi, Kenjirou [2 ]
Nagase, Hiromasa [1 ]
Endo, Tomohiro [1 ]
Moribe, Kunikazu [2 ]
Loftsson, Thorsteinn [3 ]
Yamamoto, Keiji [2 ]
Ueda, Haruhisa [1 ]
机构
[1] Hoshi Univ, Dept Phys Chem, Shinagawa Ku, Tokyo 1428501, Japan
[2] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
[3] Univ Iceland, Fac Pharm, IS-107 Reykjavik, Iceland
关键词
milling; physicochemical properties; FTIR; solid state NMR; inclusion compounds; X-ray powder diffractometry; crystallization; cyclodextrins; thermal analysis; interaction; CAMBRIDGE STRUCTURAL DATABASE; INCLUSION COMPLEXES; ALPHA-CYCLODEXTRIN; CRYSTAL-STRUCTURES; BREAKTHROUGH PAIN; GROUND MIXTURES; CANCER PAIN; ACID; WATER; CRYSTALLIZATION;
D O I
10.1002/jps.22193
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Fentanyl base and beta-cyclodextrin (beta-CD) were coground at 1: 1 and 1: 2 molar ratios (fentanyl: beta-CD) and the physicochemical characteristics of the mixtures were studied using differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), solid state C-13 nuclear magnetic resonance (NMR) spectroscopy and powder X-ray diffraction (PXRD) measurement. Additionally, portions of the coground samples were exposed to high relative humidity to investigate fentanyl and beta-CD interactions. The results of DSC and PXRD analyses indicate that the ground mixtures are in an amorphous state, and the FTIR measurements show hydrogen bonding interactions between fentanyl and beta-CD. Solid state C-13 NMR indicates that a fentanyl/beta-CD inclusion compound is formed in the humidified mixture. Furthermore, PXRD data from the humidified mixtures are similar to the PXRD patterns from the inclusion complex. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:5019-5029, 2010
引用
收藏
页码:5019 / 5029
页数:11
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