Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/28502
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dc.contributor.authorCapela, Emanuel V.pt_PT
dc.contributor.authorSantiago, Alexandre E.pt_PT
dc.contributor.authorRufino, Ana F. C. S.pt_PT
dc.contributor.authorTavares, Ana P. M.pt_PT
dc.contributor.authorPereira, Matheus M.pt_PT
dc.contributor.authorMohamadou, Aminoupt_PT
dc.contributor.authorAires-Barros, M. Raquelpt_PT
dc.contributor.authorCoutinho, João A. P.pt_PT
dc.contributor.authorAzevedo, Ana M.pt_PT
dc.contributor.authorFreire, Mara G.pt_PT
dc.date.accessioned2020-05-14T10:51:12Z-
dc.date.issued2019-
dc.identifier.issn1463-9262pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/28502-
dc.description.abstractMonoclonal antibodies (mAbs) are of crucial interest for therapeutic purposes, particularly in vaccination and immunization, and in the treatment of life-threatening diseases. However, their downstream processing from the complex cell culture media in which they are produced still requires multiple steps, making mAbs extremely high-cost products. Therefore, the development of cost-effective, sustainable and biocompatible purification strategies for mAbs is in high demand to decrease the associated economic, environmental and health burdens. Herein, novel aqueous biphasic systems (ABS) composed of glycine–betaine analogue ionic liquids (AGB-ILs) and K2HPO4/KH2PO4 at pH 7.0, the respective three-phase partitioning (TPP) systems, and hybrid processes combined with ultrafiltration were investigated and compared in terms of performance as alternative strategies for the purification and recovery of anti-human interleukin-8 (anti-IL-8) mAbs, which are specific therapeutics in the treatment of inflammatory diseases, from Chinese Hamster Ovary (CHO) cell culture supernatants. With the studied ABS, mAbs preferentially partition to the IL-rich phase, with recovery yields up to 100% and purification factors up to 1.6. The best systems were optimized in what concerns the IL concentration, allowing to take advantage of IL-based three-phase partitioning approaches where a precipitate enriched in mAbs is obtained at the ABS interface, yielding 41.0% of IgG with a purification factor of 2.7 (purity of 60.9%). Hybrid processes combining the two previous techniques and an ultrafiltration step were finally applied, allowing the recovery of mAbs from the different fractions in an appropriate buffer solution for further biopharmaceutical formulations, while allowing the simultaneous IL removal and reuse. The best results were obtained with the hybrid process combining TPP and ultrafiltration, allowing to obtain mAbs with a purity higher than 60%. The recyclability of the IL was additionally demonstrated, revealing no losses in the purification and recovery performance of these systems for mAbs. The biological activity of anti-IL-8 mAbs is maintained after the several purification and recovery steps, indicating that the novel ABS, three-phase partitioning and hybrid processes comprising AGB-ILs are promising and sustainable strategies in mAbs downstream processing.pt_PT
dc.language.isoengpt_PT
dc.publisherRoyal Society of Chemistrypt_PT
dc.relationUID/CTM/50011/2019pt_PT
dc.relationPOCI-01-0145-FEDER-030840pt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/337753/EUpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147338/PTpt_PT
dc.relationSFRH/BD/126202/2016pt_PT
dc.relationSFRH/BD/ 138997/2018pt_PT
dc.relationIF/01634/2015pt_PT
dc.relationERC-2013-StG-337753pt_PT
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739572/EUpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/135904/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleSustainable strategies based on glycine–betaine analogue ionic liquids for the recovery of monoclonal antibodies from cell culture supernatantspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage5671pt_PT
degois.publication.issue20pt_PT
degois.publication.lastPage5682pt_PT
degois.publication.titleGreen Chemistrypt_PT
dc.date.embargo2020-10-21-
dc.identifier.doi10.1039/C9GC02733Ept_PT
dc.identifier.essn1463-9270pt_PT
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