Literature DB >> 25501530

Achieving continuous manufacturing for final dosage formation: challenges and how to meet them. May 20-21, 2014 Continuous Manufacturing Symposium.

Stephen Byrn1, Maricio Futran, Hayden Thomas, Eric Jayjock, Nicola Maron, Robert F Meyer, Allan S Myerson, Michael P Thien, Bernhardt L Trout.   

Abstract

We describe the key issues and possibilities for continuous final dosage formation, otherwise known as downstream processing or drug product manufacturing. A distinction is made between heterogeneous processing and homogeneous processing, the latter of which is expected to add more value to continuous manufacturing. We also give the key motivations for moving to continuous manufacturing, some of the exciting new technologies, and the barriers to implementation of continuous manufacturing. Continuous processing of heterogeneous blends is the natural first step in converting existing batch processes to continuous. In heterogeneous processing, there are discrete particles that can segregate, versus in homogeneous processing, components are blended and homogenized such that they do not segregate. Heterogeneous processing can incorporate technologies that are closer to existing technologies, where homogeneous processing necessitates the development and incorporation of new technologies. Homogeneous processing has the greatest potential for reaping the full rewards of continuous manufacturing, but it takes long-term vision and a more significant change in process development than heterogeneous processing. Heterogeneous processing has the detriment that, as the technologies are adopted rather than developed, there is a strong tendency to incorporate correction steps, what we call below "The Rube Goldberg Problem." Thus, although heterogeneous processing will likely play a major role in the near-term transformation of heterogeneous to continuous processing, it is expected that homogeneous processing is the next step that will follow. Specific action items for industry leaders are: Form precompetitive partnerships, including industry (pharmaceutical companies and equipment manufacturers), government, and universities. These precompetitive partnerships would develop case studies of continuous manufacturing and ideally perform joint-technology development, including development of small-scale equipment and processes. Develop ways to invest internally in continuous manufacturing. How best to do this will depend on the specifics of a given organization, in particular the current development projects. Upper managers will need to energize their process developers to incorporate continuous manufacturing in at least part of their processes to gain experience and demonstrate directly the benefits. Training of continuous manufacturing technologies, organizational approaches, and regulatory approaches is a key area that industrial leaders should pursue together.
© 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

Keywords:  dispersion; downstream; drug product; drug substance; heterogeneous; homogeneous; mixing; solution; upstream

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Substances:

Year:  2014        PMID: 25501530     DOI: 10.1002/jps.24247

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  9 in total

Review 1.  An update on the contribution of hot-melt extrusion technology to novel drug delivery in the twenty-first century: part I.

Authors:  Venkata Raman Kallakunta; Sandeep Sarabu; Suresh Bandari; Roshan Tiwari; Hemlata Patil; Michael A Repka
Journal:  Expert Opin Drug Deliv       Date:  2019-05-03       Impact factor: 6.648

Review 2.  Continuous twin screw granulation - An advanced alternative granulation technology for use in the pharmaceutical industry.

Authors:  Suresh Bandari; Dinesh Nyavanandi; Venkata Raman Kallakunta; Kartik Yadav Janga; Sandeep Sarabu; Arun Butreddy; Michael A Repka
Journal:  Int J Pharm       Date:  2020-03-16       Impact factor: 5.875

3.  Pharmaceutical Co-Crystals, Salts, and Co-Amorphous Systems: A Novel Opportunity of Hot Melt Extrusion.

Authors:  Sagar Narala; Dinesh Nyavanandi; Priyanka Srinivasan; Preethi Mandati; Suresh Bandari; Michael A Repka
Journal:  J Drug Deliv Sci Technol       Date:  2020-11-09       Impact factor: 3.981

Review 4.  Coupling hot melt extrusion and fused deposition modeling: Critical properties for successful performance.

Authors:  Suresh Bandari; Dinesh Nyavanandi; Nagireddy Dumpa; Michael A Repka
Journal:  Adv Drug Deliv Rev       Date:  2021-02-09       Impact factor: 15.470

Review 5.  Advances in Twin-Screw Granulation Processing.

Authors:  Uttom Nandi; Vivek Trivedi; Steven A Ross; Dennis Douroumis
Journal:  Pharmaceutics       Date:  2021-04-27       Impact factor: 6.321

Review 6.  Continuous Formulation Approaches of Amorphous Solid Dispersions: Significance of Powder Flow Properties and Feeding Performance.

Authors:  Edina Szabó; Balázs Démuth; Dorián László Galata; Panna Vass; Edit Hirsch; István Csontos; György Marosi; Zsombor K Nagy
Journal:  Pharmaceutics       Date:  2019-12-05       Impact factor: 6.321

7.  Continuous twin screw granulation: Impact of microcrystalline cellulose batch-to-batch variability during granulation and drying - A QbD approach.

Authors:  Christoph Portier; Tamas Vigh; Giustino Di Pretoro; Jan Leys; Didier Klingeleers; Thomas De Beer; Chris Vervaet; Valérie Vanhoorne
Journal:  Int J Pharm X       Date:  2021-03-19

8.  Batch versus continuous blending of binary and ternary pharmaceutical powder mixtures.

Authors:  Maarten Jaspers; Sri Sharath Kulkarni; Florian Tegel; Timo P Roelofs; Myrthe T W de Wit; Pauline H M Janssen; Bernhard Meir; Ralf Weinekötter; Bastiaan H J Dickhoff
Journal:  Int J Pharm X       Date:  2022-01-03

Review 9.  The Future of Pharmaceutical Manufacturing Sciences.

Authors:  Jukka Rantanen; Johannes Khinast
Journal:  J Pharm Sci       Date:  2015-08-17       Impact factor: 3.534

  9 in total

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