Computer-Aided Flowsheet Simulation of a Pharmaceutical Tablet Manufacturing Process Incorporating Wet Granulation

被引:53
作者
Boukouvala, Fani [1 ]
Chaudhury, Anwesha [1 ]
Sen, Maitraye [1 ]
Zhou, Ruijie [1 ]
Mioduszewski, Lukasz [1 ]
Ierapetritou, Marianthi G. [1 ]
Ramachandran, Rohit [1 ]
机构
[1] Rutgers State Univ, Piscataway, NJ 08854 USA
基金
美国国家科学基金会;
关键词
Pharmaceutical manufacturing; Wet granulation; Flowsheet simulation; Population balance modeling; FLUIDIZED-BED; SOLIDS PROCESSES; BATCH; MODEL; DESIGN; SYSTEM; AGGLOMERATION; GRANULES; BINDER;
D O I
10.1007/s12247-012-9143-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this work, a dynamic flowsheet model for the production of pharmaceutical tablets through a continuous wet granulation process is developed. The unit operation models which are integrated to compose the process line form a hybrid configuration which is comprised of a combination of mechanistic models, population balance models, and empirical correlations, based on the currently available process knowledge for each individual component. The main objective of this study is to provide guidance in terms of the necessary steps which are required in order to move from the unit operation level to the simulation of an integrated continuous plant operation. Through this approach, not only significant process conditions for each individual process are identified but also crucial interconnecting parameters which affect critical material properties of the processed powder stream are distinguished. Through the integration of the dynamic flowsheet with a final component of tablet dissolution, the connection of the processing history of a set of powders which undergo wet granulation and are contained in each produced tablet to the release rate of the pharmaceutical ingredient is enabled. The developed flowsheet is used for the simulation of different operating scenarios and disturbances which are often encountered during operation for the assessment of their effects towards critical material attributes, product properties, and the operation of further downstream processes. Simulation results demonstrate that granulation and milling which control the particle size distribution of the processed powder mixture highly affect the hardness and dissolution of the produced tablets.
引用
收藏
页码:11 / 27
页数:17
相关论文
共 63 条
[1]  
[Anonymous], THESIS U TWENTE NETH
[2]  
Basu P., 2008, J. Pharm. Innov, V3, P30, DOI [10.1007/s12247-008-9024-4, DOI 10.1007/S12247-008-9024-4, 10.1007/S12247-008-9024-4]
[3]   Batch and continuous processing in the production of pharmaceutical granules [J].
Betz, G ;
Junker-Bürgin, P ;
Leuenberger, H .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2003, 8 (03) :289-297
[4]   A model for the drug release from a polymer matrix tablet -: effects of swelling and dissolution [J].
Borgquist, Per ;
Korner, Anna ;
Piculell, Lennart ;
Larsson, Anette ;
Axelsson, Anders .
JOURNAL OF CONTROLLED RELEASE, 2006, 113 (03) :216-225
[5]   An integrated approach for dynamic flowsheet modeling and sensitivity analysis of a continuous tablet manufacturing process [J].
Boukouvala, Fani ;
Niotis, Vasilios ;
Ramachandran, Rohit ;
Muzzio, Fernando J. ;
Ierapetritou, Marianthi G. .
COMPUTERS & CHEMICAL ENGINEERING, 2012, 42 :30-47
[6]   Computational Approaches for Studying the Granular Dynamics of Continuous Blending Processes, 2-Population Balance and Data-Based Methods [J].
Boukouvala, Fani ;
Dubey, Atul ;
Vanarase, Aditya ;
Ramachandran, Rohit ;
Muzzio, Fernando J. ;
Ierapetritou, Marianthi .
MACROMOLECULAR MATERIALS AND ENGINEERING, 2012, 297 (01) :9-19
[7]  
Boukouvala F, 2011, COMPUT-AIDED CHEM EN, V29, P216
[8]   Experimental investigation and modelling of continuous fluidized bed drying under steady-state and dynamic conditions [J].
Burgschweiger, J ;
Tsotsas, E .
CHEMICAL ENGINEERING SCIENCE, 2002, 57 (24) :5021-5038
[9]   Modeling and comparison of dissolution profiles [J].
Costa, P ;
Manuel, J ;
Lobo, S .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) :123-133
[10]  
Crowe C. T., 2006, Multiphase flow handbook