Characterization of the distribution, polymorphism, and stability of nimodipine in its solid dispersions in polyethylene glycol by micro-Raman spectroscopy and powder X-ray diffraction

被引:70
|
作者
Docoslis, Aristides [1 ]
Huszarik, Krista L.
Papageorgiou, George Z.
Bikiaris, Dimitrios
Stergiou, Anagnostis
Georgarakis, Emmanouel
机构
[1] Queens Univ, Dept Chem Engn, Kingston, ON K7L 3N6, Canada
[2] Aristotle Univ Thessaloniki, Dept Chem, Lab Organ Chem Technol, Thessaloniki 54124, Greece
[3] Aristotle Univ Thessaloniki, Dept Phys, Appl Phys Lab, Thessaloniki 54124, Greece
[4] Aristotle Univ Thessaloniki, Dept Pharm, Sect Pharmaceut & Drug Control, Thessaloniki 54124, Greece
来源
AAPS JOURNAL | 2007年 / 9卷 / 03期
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
solid dispersion; nimodipine; Raman spectroscopy; polymorphism;
D O I
10.1208/aapsj0903043
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study, a series of solid dispersions of the drug nimodipine using polyethylene glycol as carrier were prepared following the hot-melt method. Micro-Raman spectroscopy in conjunction with X-ray powder diffractometry was used for the characterization of the solid structure, including spatial distribution, physical state, and presence of polymorphs, as well as storage stability of nimodipine in its solid formulations. The effect of storage time on drug stability was investigated by examination of the samples 6 months and 18 months after preparation. Confocal micro-Raman mapping performed on the samples showed that the drug was not uniformly distributed on a microscopic level. The presence of crystals of nimodipine with sizes varying between one and several micrometers was detected, and the crystal size seemed to increase with overall drug content. In samples examined 6 months after preparation it was found that the crystals existed mainly as the racemic compound, whereas after 18 months of storage mainly crystal conglomerates were observed.
引用
收藏
页码:E361 / E370
页数:18
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