Process analysis and optimization of continuous pharmaceutical manufacturing using flowsheet models
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Zilong Wang | M. Sebastian Escotet-Espinoza | Marianthi Ierapetritou | M. Ierapetritou | Zilong Wang | M. S. Escotet-Espinoza
[1] Luc Pronzato,et al. Design of computer experiments: space filling and beyond , 2011, Statistics and Computing.
[2] Charles Cooney,et al. Regulatory and Quality Considerations for Continuous Manufacturing May 20-21, 2014 Continuous Manufacturing Symposium. , 2015, Journal of pharmaceutical sciences.
[3] G. K. Raju,et al. Understanding Pharmaceutical Quality by Design , 2014, The AAPS Journal.
[4] Mattias Björkman,et al. Global Optimization of Costly Nonconvex Functions Using Radial Basis Functions , 2000 .
[5] Krist V. Gernaey,et al. ICAS-PAT: A software for design, analysis and validation of PAT systems , 2010, Comput. Chem. Eng..
[6] Fernando J. Muzzio,et al. Characterizing continuous powder mixing using residence time distribution , 2011 .
[7] Marcus M. Edvall,et al. Tomlab - For Large-Scale Robust Optimization , 2003 .
[8] Lakshman Pernenkil,et al. A review on the continuous blending of powders , 2006 .
[9] D. Kirschner,et al. A methodology for performing global uncertainty and sensitivity analysis in systems biology. , 2008, Journal of theoretical biology.
[10] I. Sobol. Uniformly distributed sequences with an additional uniform property , 1976 .
[11] Andrew Prpich,et al. Drug product modeling predictions for scale-up of tablet film coating - A quality by design approach , 2010, Comput. Chem. Eng..
[12] H Leuenberger,et al. New trends in the production of pharmaceutical granules: batch versus continuous processing. , 2001, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[13] D. Hamby. A comparison of sensitivity analysis techniques. , 1995, Health physics.
[14] Csaba Sinka,et al. Chapter 16 Tabletting , 2007 .
[15] Derek Geldart,et al. The use of bulk density measurements as flowability indicators , 1999 .
[16] Heewon Lee. Pharmaceutical industry practices on genotoxic impurities , 2014 .
[17] Aditya U. Vanarase,et al. Real-time monitoring of drug concentration in a continuous powder mixing process using NIR spectroscopy , 2010 .
[18] Andrea Saltelli,et al. From screening to quantitative sensitivity analysis. A unified approach , 2011, Comput. Phys. Commun..
[19] Jouko Yliruusi,et al. 3D Simulation of Internal Tablet Strength During Tableting , 2011, AAPS PharmSciTech.
[20] M. Kuentz,et al. A new model for the hardness of a compacted particle system, applied to tablets of pharmaceutical polymers , 2000 .
[21] Marianthi G. Ierapetritou,et al. Discrete element reduced‐order modeling of dynamic particulate systems , 2014 .
[22] Marianthi Ierapetritou,et al. An engineering study on the enhanced control and operation of continuous manufacturing of pharmaceutical tablets via roller compaction. , 2012, International journal of pharmaceutics.
[23] K. Gernaey,et al. Good modeling practice for PAT applications: Propagation of input uncertainty and sensitivity analysis , 2009, Biotechnology progress.
[24] Jean-Loup Farges,et al. Improvement of the Representativity of the Morris Method for Air-Launch-to-Orbit Separation , 2014 .
[25] I. C. Sinka,et al. The effect of processing parameters on pharmaceutical tablet properties , 2009 .
[26] Ignacio E. Grossmann,et al. Evolution of concepts and models for quantifying resiliency and flexibility of chemical processes , 2014, Comput. Chem. Eng..
[27] Marianthi G. Ierapetritou,et al. Dynamic Data-Driven Modeling of Pharmaceutical Processes , 2011 .
[28] Marianthi Ierapetritou,et al. Implementation of an advanced hybrid MPC-PID control system using PAT tools into a direct compaction continuous pharmaceutical tablet manufacturing pilot plant. , 2014, International journal of pharmaceutics.
[29] Paola Annoni,et al. Variance based sensitivity analysis of model output. Design and estimator for the total sensitivity index , 2010, Comput. Phys. Commun..
[30] M. Ierapetritou,et al. A novel feasibility analysis method for black‐box processes using a radial basis function adaptive sampling approach , 2017 .
[31] Marianthi G. Ierapetritou,et al. Modeling of Particulate Processes for the Continuous Manufacture of Solid-Based Pharmaceutical Dosage Forms , 2013 .
[32] Andy J. Keane,et al. Engineering Design via Surrogate Modelling - A Practical Guide , 2008 .
[33] Aditya U. Vanarase,et al. Multi-dimensional population balance modeling and experimental validation of continuous powder mixing processes , 2012 .
[34] Marianthi G. Ierapetritou,et al. Computational Approaches for Studying the Granular Dynamics of Continuous Blending Processes, 2 – Population Balance and Data‐Based Methods , 2012 .
[35] Fernando J. Muzzio,et al. Effects of powder flow properties and shear environment on the performance of continuous mixing of pharmaceutical powders , 2013 .
[36] Lawrence X. Yu. Pharmaceutical Quality by Design: Product and Process Development, Understanding, and Control , 2008, Pharmaceutical Research.
[37] Marianthi G. Ierapetritou,et al. Surrogate-Based Optimization of Expensive Flowsheet Modeling for Continuous Pharmaceutical Manufacturing , 2013, Journal of Pharmaceutical Innovation.
[38] Marianthi G. Ierapetritou,et al. Feasibility and flexibility analysis of black-box processes Part 1: Surrogate-based feasibility analysis , 2015 .
[39] I. Sobol. On the distribution of points in a cube and the approximate evaluation of integrals , 1967 .
[40] M. D. McKay,et al. A comparison of three methods for selecting values of input variables in the analysis of output from a computer code , 2000 .
[41] Jose E. Tabora,et al. Modeling-Based Approach Towards Quality by Design for the Ibipinabant API Step , 2012 .
[42] Marianthi G. Ierapetritou,et al. An Integrated Approach to Simulation of Pharmaceutical Processes for Solid Drug Manufacture , 2014 .
[43] Atul Dubey,et al. Mathematical Development and Comparison of a Hybrid PBM-DEM Description of a Continuous Powder Mixing Process , 2013 .
[44] Gowtham Kumar . Dokala,et al. Direct Compression - An Overview , 2013 .
[45] Massimo Morbidelli,et al. Model-based design space determination of peptide chromatographic purification processes. , 2013, Journal of chromatography. A.
[46] Marianthi G. Ierapetritou,et al. An integrated approach for dynamic flowsheet modeling and sensitivity analysis of a continuous tablet manufacturing process , 2012, Comput. Chem. Eng..
[47] F. Bertrand,et al. DEM-based models for the mixing of granular materials , 2005 .
[48] Marianthi G. Ierapetritou,et al. Computational Approaches for Studying the Granular Dynamics of Continuous Blending Processes, 1 – DEM Based Methods , 2011 .
[49] Andre Raw,et al. Quality by Design: Concepts for ANDAs , 2008, The AAPS Journal.
[50] Rafael Méndez,et al. Particle size segregation promoted by powder flow in confined space: The die filling process case , 2014 .
[51] Fernando J. Muzzio,et al. Method for characterization of loss-in-weight feeder equipment , 2012 .
[52] A. Cuitiño,et al. Modeling and simulation of compact strength due to particle bonding using a hybrid discrete-continuum approach. , 2011, International journal of pharmaceutics.
[53] Fernando J. Muzzio,et al. A review of the Residence Time Distribution (RTD) applications in solid unit operations , 2012 .
[54] Lawrence X. Yu,et al. Modernizing Pharmaceutical Manufacturing: from Batch to Continuous Production , 2015, Journal of Pharmaceutical Innovation.
[55] Fernando J. Muzzio,et al. Investigation on the effect of blade patterns on continuous solid mixing performance , 2011 .
[56] Dimitrios I. Gerogiorgis,et al. Economic Analysis of Integrated Continuous and Batch Pharmaceutical Manufacturing: A Case Study , 2011 .
[57] Fani Boukouvala,et al. Computer-Aided Flowsheet Simulation of a Pharmaceutical Tablet Manufacturing Process Incorporating Wet Granulation , 2013, Journal of Pharmaceutical Innovation.
[58] Ravendra Singh,et al. Multi-scale flowsheet simulation of an integrated continuous purification-downstream pharmaceutical manufacturing process. , 2013, International journal of pharmaceutics.
[59] Kimio Kawakita,et al. Some considerations on powder compression equations , 1971 .
[60] G. Reklaitis,et al. Perspectives on the continuous manufacturing of powder‐based pharmaceutical processes , 2016 .
[61] B. Iooss,et al. A Review on Global Sensitivity Analysis Methods , 2014, 1404.2405.
[62] Rajesh N. Dave,et al. Discrete element method simulation of a conical screen mill: A continuous dry coating device , 2015 .
[63] Saltelli Andrea,et al. Global Sensitivity Analysis: The Primer , 2008 .
[64] Marianthi G. Ierapetritou,et al. Design Space of Pharmaceutical Processes Using Data-Driven-Based Methods , 2010, Journal of Pharmaceutical Innovation.
[65] Runyu Yang,et al. Discrete particle simulation of particulate systems: A review of major applications and findings , 2008 .
[66] Fernando J. Muzzio,et al. Feedrate deviations caused by hopper refill of loss-in-weight feeders , 2015 .
[67] Dana Barrasso,et al. A comparison of model order reduction techniques for a four-dimensional population balance model describing multi-component wet granulation processes , 2012 .
[68] Bernhardt L Trout,et al. Achieving Continuous Manufacturing for Final Dosage Formation: Challenges and How to Meet Them May 20-21 2014 Continuous Manufacturing Symposium. , 2015, Journal of pharmaceutical sciences.
[69] Marianthi G. Ierapetritou,et al. Periodic section modeling of convective continuous powder mixing processes , 2012 .
[70] Metin Çelik,et al. Pharmaceutical Powder Compaction Technology , 2016 .