期刊
JOURNAL OF PHARMACEUTICAL INNOVATION
卷 16, 期 1, 页码 181-196出版社
SPRINGER
DOI: 10.1007/s12247-020-09433-5
关键词
Powder flow; Static image analysis; Continuous direct compression; Modelling; Shear cell; Powder surface area
资金
- Finance Birmingham (UK) as part of the AMSCI initiative
The study focused on understanding and predicting the flow of bulk pharmaceutical materials for pharmaceutical manufacturing by continuous direct compression (CDC). By analyzing particle properties, powder measurements and using statistical modeling, researchers were able to build predictive models for flow. Results showed that static image analysis could predict flow in shear cells related to performance in a CDC system, with little powder needed for analysis, while surface area and surface energy techniques did not significantly contribute to the precision of the model.
Purpose Understanding and predicting the flow of bulk pharmaceutical materials could be key in enabling pharmaceutical manufacturing by continuous direct compression (CDC). This study examines whether, by taking powder and bulk measurements, and using statistical modelling, it would be possible to predict the flow of a range of materials likely to be used in CDC. Methods More than 100 materials were selected for study, from four pharmaceutical companies. Particle properties were measured by static image analysis, powder surface area and surface energy techniques, and flow by shear cell measurements. The data was then analysed, and a range of statistical modelling techniques were used to build predictive models for flow. Results Using the results from static image analysis, a model could be built which allowed the prediction of likely flow in a shear cell, which can be related to performance in a CDC system. Only a small amount of powder was required for the image analysis. Surface area did not add to the precision of the model, and the available surface energy technique did not correlate with flow. Conclusions A small sample of powder can be examined by static image analysis, and this data can be used to give an early read on likely flow of a material in a CDC system or other pharmaceutical process, allowing early intervention (if necessary) to improve the characteristics of a material, early in development.
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