Application of principal component analysis enables to effectively find important physical variables for optimization of fluid bed granulator conditions.

Principal component analysis was applied to effectively optimize the operational conditions of a fluidized bed granulator for preparing granules with excellent compaction and tablet physical properties. The crucial variables that affect the properties of the granules, their compactability and the resulting tablet properties were determined through analysis of a series of granulation and tabletting experiments. Granulation was performed while the flow rate and concentration of the binder were changed as independent operational variables, according to a two-factor central composite design. Thirteen physicochemical properties of granules and tablets were examined: powder properties (particle size, size distribution width, Carr's index, Hausner ratio and aspect ratio), compactability properties (pressure transmission ratio, die wall force and ejection force) and tablet properties (tensile strength, friability, disintegration time, weight variation and drug content uniformity). Principal component analysis showed that the pressure transmission ratio, die wall force and Carr's index were the most important variables in granule preparation. Multiple regression analysis also confirmed these results. Furthermore, optimized operational conditions obtained from the multiple regression analysis enabled the production of granules with desirable properties for tabletting. This study presents the first use of principle component analysis for identifying and successfully predicting the most important variables in the process of granulation and tabletting.

[1]  J.A.H. de Jong,et al.  Tablet properties as a function of the properties of granules made in a fluidized bed process , 1991 .

[2]  G. C. Dacanal,et al.  Selection of operational parameters for the production of instant soy protein isolate by pulsed fluid bed agglomeration , 2010 .

[3]  C. C. Furnasz Grading Aggregates I-Mathematical Relations for Beds of Broken Solids of Maximum Density ’ , ’ , 2022 .

[4]  Jouko Yliruusi,et al.  Granule size control and targeting in pulsed spray fluid bed granulation. , 2009, International journal of pharmaceutics.

[5]  F. Stillinger,et al.  Improving the Density of Jammed Disordered Packings Using Ellipsoids , 2004, Science.

[6]  Ingunn Tho,et al.  Application of multivariate methods to compression behavior evaluation of directly compressible materials. , 2009, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[7]  D L Massart,et al.  Using experimental design to optimize the process parameters in fluidized bed granulation on a semi-full scale. , 2001, International journal of pharmaceutics.

[8]  G. Alderborn,et al.  Compression characteristics of granulated materials. IV. The effect of granule porosity on the fragmentation propensity and the compatibility of some granulations , 1991 .

[9]  Kozo Takayama,et al.  Formulation design of indomethacin gel ointment containing d-limonene using computer optimization methodology , 1990 .

[10]  S. Itai,et al.  Optimization of a novel wax matrix system using aminoalkyl methacrylate copolymer E and ethylcellulose to suppress the bitter taste of acetaminophen. , 2010, International journal of pharmaceutics.

[11]  G. Peck,et al.  Development of agglomerated talc. I: Evaluation of fluidized bed granulation parameters on the physical properties of agglomerated talc , 1995 .

[12]  Y. Kawashima,et al.  Die wall pressure measurement for evaluation of compaction property of pharmaceutical materials. , 2004, International journal of pharmaceutics.

[13]  Å. Rasmuson,et al.  Particle size distribution and evolution in tablet structure during and after compaction. , 2005, International journal of pharmaceutics.

[14]  Ragnar Ek,et al.  Compression behaviour and compactability of microcrystalline cellulose pellets in relationship to their pore structure and mechanical properties , 1995 .

[15]  K. Leiviskä,et al.  Influence of granulation and compression process variables on flow rate of granules and on tablet properties, with special reference to weight variation , 1994 .

[16]  H. Sunada,et al.  Effect of Several Cellulosic Binders on Particle Size Distribution in Fluidized Bed Granulation. , 1995 .

[17]  J. Newton,et al.  Determination of tablet strength by the diametral-compression test. , 1970, Journal of pharmaceutical sciences.

[18]  Ian T. Jolliffe,et al.  Principal Component Analysis , 2002, International Encyclopedia of Statistical Science.

[19]  P. Vonk,et al.  Fluid bed agglomeration with a narrow droplet size distribution. , 2000, International journal of pharmaceutics.

[20]  Eric Doelker,et al.  Benefits of die-wall instrumentation for research and development in tabletting. , 2004, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[21]  R L Carr,et al.  EVALUATING FLOW PROPERTIES OF SOLIDS , 1965 .