Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/25501

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Campo DCValorIdioma
dc.contributor.authorRodrigues, E.-
dc.contributor.authorCosta, A. R.-
dc.contributor.authorHenriques, Mariana-
dc.contributor.authorCunnah, Philip-
dc.contributor.authorMelton, David-
dc.contributor.authorAzeredo, Joana-
dc.contributor.authorOliveira, Rosário-
dc.date.accessioned2013-10-04T14:35:54Z-
dc.date.available2013-10-04T14:35:54Z-
dc.date.issued2013-
dc.identifier.issn0273-2289por
dc.identifier.urihttps://hdl.handle.net/1822/25501-
dc.description.abstractCurrently, mammalian cell technology has become the focus of biopharmaceutical production, with strict regulatory scrutiny of the techniques employed. Major concerns about the presence of animal-derived components in the culture media led to the development of serum-free (SF) culture processes. However, cell adaptation to SF conditions is still a major challenge and limiting step of process development. Thus, this study aims to assess the impact of SF adaptation on monoclonal antibody production (mAb), identify the most critical steps of cell adaptation to the SF EX-CELL medium, and create basic process guidelines.. The success of SF adaptation was dependent on critical steps that included: accentuated cell sensitivity to common culture procedures (centrifugation, trypsinization); initial cell concentration; time given at each step of serum-reduction; and, most importantly, medium supplements used to support adaptation. Indeed, only one of the five supplement combinations assessed (rhinsulin, ammonium metavanadate, nickel chloride and stannous chloride) succeeded for the CHO-K1 cell line used. This work also revealed that the chemically-defined EX-CELL medium benefits mAb production in comparison with the general purpose Dulbecco's Modified Eagle's Medium, but the complete removal of serum attenuates these positive effects.por
dc.description.sponsorshipThe authors acknowledge funding and support from the Portuguese Foundation for Science and Technology (FCT), namely grant ref SFRH/BD/46661/2008 for Maria Elisa Rodrigues and SFRH/BD/46660/2008 for Ana Rita Costa.por
dc.language.isoengpor
dc.publisherSpringerpor
dc.rightsopenAccesspor
dc.subjectChinese hamster ovary cellspor
dc.subjectMonoclonal antibodypor
dc.subjectProductionpor
dc.subjectSerum-free mediumpor
dc.subjectTrace elementspor
dc.subjectCell adaptationpor
dc.titleAdvances and drawbacks of the adaptation to serum-free culture of CHO-K1 cells for monoclonal antibody productionpor
dc.typearticlepor
dc.peerreviewedyespor
sdum.publicationstatuspublishedpor
oaire.citationStartPage1279por
oaire.citationEndPage1291por
oaire.citationIssue4por
oaire.citationTitleApplied Biochemistry and Biotechnology - Part A Enzyme Engineering and Biotechnologypor
oaire.citationVolume169por
dc.publisher.uriHumana Press, Inc.por
dc.identifier.doi10.1007/s12010-012-0068-zpor
dc.identifier.pmid23306891por
dc.subject.wosScience & Technologypor
sdum.journalApplied Biochemistry and Biotechnologypor
Aparece nas coleções:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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