佀国宁, 陈岚, 李保国. 基于Kawakita方程的多元药物粉体直压特性的理论预测模型J. 药学学报, 2014,49(4): 550-557.
引用本文: 佀国宁, 陈岚, 李保国. 基于Kawakita方程的多元药物粉体直压特性的理论预测模型J. 药学学报, 2014,49(4): 550-557.
SI Guo-ning, CHEN Lan, LI Bao-guo. Theoretical modeling and experimental research on direct compaction characteristics of multi-component pharmaceutical powders based on the Kawakita equationJ. Acta Pharmaceutica Sinica, 2014,49(4): 550-557.
Citation: SI Guo-ning, CHEN Lan, LI Bao-guo. Theoretical modeling and experimental research on direct compaction characteristics of multi-component pharmaceutical powders based on the Kawakita equationJ. Acta Pharmaceutica Sinica, 2014,49(4): 550-557.

基于Kawakita方程的多元药物粉体直压特性的理论预测模型

Theoretical modeling and experimental research on direct compaction characteristics of multi-component pharmaceutical powders based on the Kawakita equation

  • 摘要: 应用Kawakita粉体压缩方程,建立了适用于多种成分和不同质量百分比的药物粉体混合物压缩特性的通用理论预测模型。分别对乳糖、淀粉和微晶纤维素3种常用辅料进行了单向圆片直压实验,并求得相应辅料的Kawakita方程参数。对含有不同质量百分比的乳糖、淀粉、微晶纤维素和硬脂富马酸钠5种药物粉体混合物进行了单向圆片直压实验,得到了混合物密度随压力的变化规律和Kawakita方程曲线。最后将理论预测模型结果与实验结果进行对比。结果表明,不同比例混合物密度的误差绝对值在5% 内,Kawakita曲线纵坐标误差绝对值均保持在4.6% 内,验证了该理论模型能够用于预测多元药物粉体直压特性。

     

    Abstract: Base on the Kawakita powder compression equation, a general theoretical model for predicting the compression characteristics of multi-components pharmaceutical powders with different mass ratios was developed. The uniaxial flat-face compression tests of powder lactose, starch and microcrystalline cellulose were carried out, separately. Therefore, the Kawakita equation parameters of the powder materials were obtained. The uniaxial flat-face compression tests of the powder mixtures of lactose, starch, microcrystalline cellulose and sodium stearyl fumarate with five mass ratios were conducted, through which, the correlation between mixture density and loading pressure and the Kawakita equation curves were obtained. Finally, the theoretical prediction values were compared with experimental results. The analysis showed that the errors in predicting mixture densities were less than 5.0% and the errors of Kawakita vertical coordinate were within 4.6%, which indicated that the theoretical model could be used to predict the direct compaction characteristics of multi-component pharmaceutical powders.

     

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