INHIBITION OF INDOMETHACIN CRYSTALLIZATION IN POLY(VINYLPYRROLIDONE) COPRECIPITATES

被引:227
作者
YOSHIOKA, M [1 ]
HANCOCK, BC [1 ]
ZOGRAFI, G [1 ]
机构
[1] UNIV WISCONSIN,SCH PHARM,MADISON,WI 53706
基金
英国惠康基金;
关键词
D O I
10.1002/jps.2600840814
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Differential scanning calorimetry and powder X-ray diffraction studies have been carried out with amorphous coprecipitates of indomethacin and poly(vinylpyrrolidone), PVP, to measure the glass transition temperature, T-g, as a function of mixture composition and the nonisothermal and isothermal crystallization of the indomethacin. Values of T-g as a function of mixture composition followed the ideal Gordon-Taylor equation up to about 50% w/w PVP. Inhibition of crystallization occurred at levels as low as 5% PVP and very significant inhibition was observed at and above 20% PVP. Inhibition of crystallization of indomethacin in the absence of PVP required a storage temperature 40-50 degrees C below T-g, whereas comparable inhibition with PVP was observed at storage temperatures 5 degrees C above T-g. This suggests that the inhibition of indomethacin crystallization by PVP may involve mechanisms other than just the general antiplasticizing effect (raising T-g) by PVP.
引用
收藏
页码:983 / 986
页数:4
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