Integrated continuous process design for crystallisation, spherical agglomeration, and filtration of lovastatin
Brown, Cameron J. and McGinty, John and Islam, Muhammad T. and Rajoub, Nazer and Arjmandi-Tash, Omid and Ottoboni, Sara and Shahid, Muhid and Urwin, Stephanie J. and Lee, Ye Seol and Chong, Magdalene W. S. and Papathanasiou, Foteini and Prakash, Aruna S. and Prasad, Elke and Spence, Bronwyn and Sefcik, Jan and Robertson, John and Smith, Rachel and Litster, James D. and Price, Chris J. and Nordon, Alison and Adjiman, Claire S. and Florence, Alastair J. (2024) Integrated continuous process design for crystallisation, spherical agglomeration, and filtration of lovastatin. Journal of Pharmaceutical Innovation, 19 (2). 9. ISSN 1939-8042 (https://doi.org/10.1007/s12247-024-09815-z)
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Abstract
Purpose This work seeks to improve the particle processability of needle-like lovastatin crystals and develop a small-footprint continuous MicroFactory for its production. Methods General conditions for optimal spherical agglomeration of lovastatin crystals and subsequent product isolation are developed, first as batch processes, and then transferred to continuous MicroFactory operation. Results Methyl isobutyl ketone is a suitable bridging liquid for the spherical agglomeration of lovastatin. Practical challenges including coupling unit operations and solvent systems; mismatched flow rates and inconsistent suspension solid loading were resolved. The successful continuous production of lovastatin spherical agglomerates (D50 = 336 µm) was achieved. Spherical agglomeration increased the density of the bulk lovastatin powder and improved product flowability from poor to good, whilst maintaining lovastatin tablet performance. Conclusion A continuous, integrated MicroFactory for the crystallisation, spherical agglomeration, and filtration of lovastatin is presented with improved product particle processability. Up to 16,800 doses of lovastatin (60 mg) can be produced per day using a footprint of 23 m2.
ORCID iDs
Brown, Cameron J. ORCID: https://orcid.org/0000-0001-7091-1721, McGinty, John ORCID: https://orcid.org/0000-0002-8166-7266, Islam, Muhammad T. ORCID: https://orcid.org/0000-0002-3530-0519, Rajoub, Nazer ORCID: https://orcid.org/0000-0002-1373-3022, Arjmandi-Tash, Omid, Ottoboni, Sara ORCID: https://orcid.org/0000-0002-2792-3011, Shahid, Muhid, Urwin, Stephanie J. ORCID: https://orcid.org/0000-0002-9092-0200, Lee, Ye Seol, Chong, Magdalene W. S., Papathanasiou, Foteini, Prakash, Aruna S. ORCID: https://orcid.org/0000-0001-7368-3875, Prasad, Elke ORCID: https://orcid.org/0000-0002-5412-9374, Spence, Bronwyn, Sefcik, Jan ORCID: https://orcid.org/0000-0002-7181-5122, Robertson, John ORCID: https://orcid.org/0000-0002-2191-1319, Smith, Rachel, Litster, James D., Price, Chris J. ORCID: https://orcid.org/0000-0002-0790-6003, Nordon, Alison ORCID: https://orcid.org/0000-0001-6553-8993, Adjiman, Claire S. and Florence, Alastair J. ORCID: https://orcid.org/0000-0002-9706-8364;-
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Item type: Article ID code: 88305 Dates: DateEvent1 March 2024Published2 February 2024Accepted29 November 2023SubmittedSubjects: Medicine > Pharmacy and materia medica Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Faculty of Engineering > Chemical and Process Engineering
Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > Continuous Manufacturing and Crystallisation (CMAC)
Technology and Innovation Centre > Bionanotechnology
Strategic Research Themes > Measurement Science and Enabling Technologies
Strategic Research Themes > Advanced Manufacturing and MaterialsDepositing user: Pure Administrator Date deposited: 01 Mar 2024 11:33 Last modified: 11 Nov 2024 14:09 URI: https://strathprints.strath.ac.uk/id/eprint/88305