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Closing the gap in series scale up of high shear wet granulation process using impeller power and blade design
Authors:Gossett A. Campbell  Donald J. Clancy  Jinzhou X. Zhang  Manish K. Gupta  Choon K. Oh
Affiliation:1. Pharmaceutical Materials Science and Engineering Laboratory, Department of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota 55455;2. Eli Lilly and Company, Indianapolis, Indiana 46285;1. Drug Product Science & Technology, Bristol-Myers Squibb New Brunswick, New Jersey 08901;2. Analytical & Bioanalytical Development, Bristol-Myers Squibb New Brunswick, New Jersey 08901
Abstract:This paper investigates the use of impeller work combined with an understanding of the significance of the impeller power inflection point during granulation to monitor, control, and scale up high shear wet granulation processes in the pharmaceutical industry. High shear wet granulations were carried out in a series of PMA Fielder granulators (25, 65, 150, and 300-L) with a geometric similar bowl at conditions of constant water addition time and constant tip speed. The results suggested that the granulation process can be effectively scaled up using a linear relationship between the impeller power inflection point (percent of water added at the point where the impeller load starts rising) and the Froude number in PMA Fielder granulator. To close the gap in the series scale up of wet granulation processes, it is desirable to design a granulator at small scale that performs similarly to a full scale commercial granulator such that no variables have to be significantly changed during scale up. A customized 6-L granulator (Fluid Air, Inc.) was designed with a similar bowl geometry as the 300-L Fielder granulator with a specialized blade of lower angle. It is illustrated in this paper that a 6-L granulator can be directly scaled up to a 300-L granulator using constant tip speed and percentage water addition, with the same impeller work and drug product performance. Granulation scale up using the impeller power as the endpoint measurement, combined with a proper impeller blade design can significantly reduce expenditure and time and accelerate the progression of drug product to market, by eliminating stepwise series scale up, and minimizing drug substance requirements.
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