Technoeconomic Evaluation of Multiple Mixed Suspension-Mixed Product Removal (MSMPR) Crystallizer Configurations for Continuous Cyclosporine Crystallization

被引:12
作者
Diab, Samir [1 ]
Gerogiorgis, Dimitrios I. [1 ]
机构
[1] Univ Edinburgh, Sch Engn, Inst Mat & Proc, Kings Bldg, Edinburgh EH9 3FB, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
ACTIVE PHARMACEUTICAL INGREDIENTS; ANTISOLVENT CRYSTALLIZATION; PLUG-FLOW; BATCH; DESIGN; SEPARATION; OPTIMIZATION; SELECTION; INDUSTRY; APIS;
D O I
10.1021/acs.oprd.7b00225
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Continuous crystallization using Mixed Suspension-Mixed Product Removal (MSMPR) crystallizers has been demonstrated as a feasible method for implementing continuous separations in pharmaceutical manufacturing processes. This work conducts a steady-state process modeling and simulation study of the continuous cooling crystallization of cyclosporine, comparing processes with and without solids recycle for their technoeconomic viability. The model describes population balance equations, crystallization kinetics, and process mass balances to compare attainable crystallization and plant wide yields of different process configurations. Total cost components using an established economic analysis methodology are compared for varying numbers of crystallizers, operating temperatures, total crystallizer cascade residence times and API feed concentrations. Economic analyses and the calculation of normalized cost components with respect to total crystallizer volumes identify the process without recycle as the most economically viable option, achieving the lowest total costs and low E-factors for pharmaceutical processes. The sensitivity of total costs to the selected total residence times for economic analyses highlights the need for rigorous comparison methodologies. This work identifies the need for technoeconomic optimization studies of continuous crystallization processes to establish the optimal design of manufacturing campaigns prior to further development.
引用
收藏
页码:1571 / 1587
页数:17
相关论文
共 73 条
[1]   Evaluation of mixed suspension mixed product removal crystallization processes coupled with a continuous filtration system [J].
Acevedo, David ;
Pena, Ramon ;
Yang, Yang ;
Barton, Alastair ;
Firth, Paul ;
Nagy, Zoltan K. .
CHEMICAL ENGINEERING AND PROCESSING-PROCESS INTENSIFICATION, 2016, 108 :212-219
[2]   On-demand continuous-flow production of pharmaceuticals in a compact, reconfigurable system [J].
Adamo, Andrea ;
Beingessner, Rachel L. ;
Behnam, Mohsen ;
Chen, Jie ;
Jamison, Timothy F. ;
Jensen, Klavs F. ;
Monbaliu, Jean-Christophe M. ;
Myerson, Allan S. ;
Revalor, Eve M. ;
Snead, David R. ;
Stelzer, Torsten ;
Weeranoppanant, Nopphon ;
Wong, Shin Yee ;
Zhang, Ping .
SCIENCE, 2016, 352 (6281) :61-67
[3]   Crystallization of Cyclosporine in a Multistage Continuous MSMPR Crystallizer [J].
Alvarez, Alejandro J. ;
Singh, Aniruddh ;
Myerson, Allan S. .
CRYSTAL GROWTH & DESIGN, 2011, 11 (10) :4392-4400
[4]   Continuous Plug Flow Crystallization of Pharmaceutical Compounds [J].
Alvarez, Alejandro J. ;
Myerson, Allan S. .
CRYSTAL GROWTH & DESIGN, 2010, 10 (05) :2219-2228
[5]   Separation of Active Pharmaceutical Ingredients (APIs) from Excipients in Pharmaceutical Formulations [J].
Atwood, Jerry L. .
CRYSTAL GROWTH & DESIGN, 2015, 15 (06) :2874-2877
[6]   The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry [J].
Baumann, Marcus ;
Baxendale, Ian R. .
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2015, 11 :1194-1219
[7]   Modeling a seeded continuous crystallizer for the production of active pharmaceutical ingredients [J].
Besenhard, M. O. ;
Hohl, R. ;
Hodzic, A. ;
Eder, R. J. P. ;
Khinast, J. G. .
CRYSTAL RESEARCH AND TECHNOLOGY, 2014, 49 (2-3) :92-108
[8]   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
[9]  
Braden T.M., 2009, World Patent, Patent No. [023515 A2, 023515]
[10]   From Batch to Continuous Flow Processing in Chemicals Manufacturing [J].
Calabrese, Gary S. ;
Pissavini, Sergio .
AICHE JOURNAL, 2011, 57 (04) :828-834