On-demand continuous-flow production of pharmaceuticals in a compact, reconfigurable system

Andrea Adamo(Massachusetts Institute of Technology), Rachel L. Beingessner(Massachusetts Institute of Technology), Mohsen Behnam(Massachusetts Institute of Technology), Jie Chen(Massachusetts Institute of Technology), Timothy F. Jamison(Massachusetts Institute of Technology), Klavs F. Jensen(Massachusetts Institute of Technology), Jean‐Christophe M. Monbaliu(Massachusetts Institute of Technology), Allan S. Myerson(Massachusetts Institute of Technology), Eve Revalor(Massachusetts Institute of Technology), David R. Snead(Massachusetts Institute of Technology), Torsten Stelzer(Massachusetts Institute of Technology), Nopphon Weeranoppanant(Massachusetts Institute of Technology), Shin Yee Wong(Massachusetts Institute of Technology), Ping Zhang(Massachusetts Institute of Technology)
Science
March 31, 2016
Cited by 935

Abstract

Pharmaceutical manufacturing typically uses batch processing at multiple locations. Disadvantages of this approach include long production times and the potential for supply chain disruptions. As a preliminary demonstration of an alternative approach, we report here the continuous-flow synthesis and formulation of active pharmaceutical ingredients in a compact, reconfigurable manufacturing platform. Continuous end-to-end synthesis in the refrigerator-sized [1.0 meter (width) × 0.7 meter (length) × 1.8 meter (height)] system produces sufficient quantities per day to supply hundreds to thousands of oral or topical liquid doses of diphenhydramine hydrochloride, lidocaine hydrochloride, diazepam, and fluoxetine hydrochloride that meet U.S. Pharmacopeia standards. Underlying this flexible plug-and-play approach are substantial enabling advances in continuous-flow synthesis, complex multistep sequence telescoping, reaction engineering equipment, and real-time formulation.


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