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dc.contributor.authorCrowell, Laura E
dc.contributor.authorLu, Amos E
dc.contributor.authorLove, Kerry R
dc.contributor.authorStockdale, Alan
dc.contributor.authorTimmick, Steven M
dc.contributor.authorWu, Di
dc.contributor.authorWang, Yu Annie
dc.contributor.authorDoherty, William
dc.contributor.authorBonnyman, Alexandra
dc.contributor.authorVecchiarello, Nicholas
dc.contributor.authorGoodwine, Chaz
dc.contributor.authorBradbury, Lisa
dc.contributor.authorBrady, Joseph R
dc.contributor.authorClark, John J
dc.contributor.authorColant, Noelle A
dc.contributor.authorCvetkovic, Aleksandar
dc.contributor.authorDalvie, Neil C
dc.contributor.authorLiu, Diana
dc.contributor.authorLiu, Yanjun
dc.contributor.authorMascarenhas, Craig A
dc.contributor.authorMatthews, Catherine B
dc.contributor.authorMozdzierz, Nicholas J
dc.contributor.authorShah, Kartik A
dc.contributor.authorWu, Shiaw-Lin
dc.contributor.authorHancock, William S
dc.contributor.authorBraatz, Richard D
dc.contributor.authorCramer, Steven M
dc.contributor.authorLove, J Christopher
dc.date.accessioned2021-10-27T20:08:49Z
dc.date.available2021-10-27T20:08:49Z
dc.date.issued2018
dc.identifier.urihttps://hdl.handle.net/1721.1/134719
dc.description.abstract© 2018, Nature Publishing Group. All rights reserved. Conventional manufacturing of protein biopharmaceuticals in centralized, large-scale, single-product facilities is not well-suited to the agile production of drugs for small patient populations or individuals. Previous solutions for small-scale manufacturing are limited in both process reproducibility and product quality, owing to their complicated means of protein expression and purification1–4. We describe an automated, benchtop, multiproduct manufacturing system, called Integrated Scalable Cyto-Technology (InSCyT), for the end-to-end production of hundreds to thousands of doses of clinical-quality protein biologics in about 3 d. Unlike previous systems, InSCyT includes fully integrated modules for sustained production, efficient purification without the use of affinity tags, and formulation to a final dosage form of recombinant biopharmaceuticals. We demonstrate that InSCyT can accelerate process development from sequence to purified drug in 12 weeks. We used integrated design to produce human growth hormone, interferon a-2b and granulocyte colony-stimulating factor with highly similar processes on this system and show that their purity and potency are comparable to those of marketed reference products.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.relation.isversionof10.1038/NBT.4262
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourcePMC
dc.titleOn-demand manufacturing of clinical-quality biopharmaceuticals
dc.typeArticle
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.relation.journalNature Biotechnology
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-08-14T18:38:22Z
dspace.orderedauthorsCrowell, LE; Lu, AE; Love, KR; Stockdale, A; Timmick, SM; Wu, D; Wang, YA; Doherty, W; Bonnyman, A; Vecchiarello, N; Goodwine, C; Bradbury, L; Brady, JR; Clark, JJ; Colant, NA; Cvetkovic, A; Dalvie, NC; Liu, D; Liu, Y; Mascarenhas, CA; Matthews, CB; Mozdzierz, NJ; Shah, KA; Wu, S-L; Hancock, WS; Braatz, RD; Cramer, SM; Love, JC
dspace.date.submission2019-08-14T18:38:23Z
mit.journal.volume36
mit.journal.issue10
mit.metadata.statusAuthority Work and Publication Information Needed


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