Plantwide design and economic evaluation of two Continuous Pharmaceutical Manufacturing (CPM) cases: Ibuprofen and artemisinin

被引:58
|
作者
Jolliffe, Hikaru G. [1 ]
Gerogiorgis, Dimitrios I. [1 ]
机构
[1] Univ Edinburgh, IMP, Sch Engn, 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
Continuous Pharmaceutical Manufacturing (CPM); Ibuprofen; Artemisinin; Process design; Reactor design; Separation design; CONTINUOUS-FLOW SYNTHESIS; SEMISYNTHETIC ARTEMISININ; GREEN CHEMISTRY; BATCH; EFFICIENCY; CRYSTALLIZATION; MICROREACTORS; INDUSTRY;
D O I
10.1016/j.compchemeng.2016.04.005
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Increasing Research and Development (R&D) costs, growing competition from generic manufacturers and dwindling market introduction rates for novel drug products bolster the efforts of pharmaceutical firms to secure competitiveness by investigating Continuous Pharmaceutical Manufacturing (CPM). The present paper explores the CPM of two key Active Pharmaceutical Ingredients (APIs), ibuprofen and artemisinin: cost savings and material efficiency benefits are evaluated for CPM vs. batch processing, with two continuous options for each API. Capital Expenditure (CapEx) savings of up to 57.0% and 19.6% and corresponding Operating Expenditure (OpEx) savings of up to 51.6% and 29.3% have been determined for ibuprofen and artemisinin, respectively. Total projected cost savings for a 20-year plant lifetime can reach 54.5% and 20.1%, respectively. Environmental (E)-factors (mass of waste generated per unit mass of product) of 43.4 (for ibuprofen) and 12.2 (for artemisinin) have been computed, indicating environmental and material efficiency advantages for these conceptual continuous pharmaceutical processes. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:269 / 288
页数:20
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