Continuous perfusion culture of encapsulated hybridoma cells

Martí Lecina, Albert Tintó, Jordi Gálvez, Francesc Gòdia, Jordi J. Cairó

    Research output: Contribution to journalArticleResearchpeer-review

    7 Citations (Scopus)


    Background: The production of Monoclonal antibodies (mAbs) is often performed in batch or fed-batch operations where low cell densities and low volumetric productivities are achieved. The main bottleneck of both processes is the short operating time with productive cells at maximum cell concentration. Results: The process studied in this work is based on a fluidized-bed bioreactor culture of encapsulated KB26.5 cells in a liquid core of calcium alginate microcapsules as a culture strategy to produce IgG3. First, DMEM medium was modified in order to protect the microcapsules from degradation, and later, the optimal operating conditions were set. Under these conditions encapsulated KB26.5 cells reached cell densities of 1.05 × 108cells mL-1 or 9.8 × 106 cells mL-1 (referred to the inner capsule volume or total bioreactor volume, respectively), and a mAb volumetric productivity of 2.75 μg mL-1 h-1. Conclusions: The productivity of encapsulated KB26.5 cells in perfusion culture was enhanced significantly in comparison with batch and fed-batch processes. Continuous operation of the perfusion culture for periods longer than 35 days, represented a volumetric productivity about five-fold higher than conventional operations. However, the fluidized-bed also showed limitations such as low cell viability at high cell densities due to the mass transfer limitations of large molecules inside the microcapsules. © 2011 Society of Chemical Industry.
    Original languageEnglish
    Pages (from-to)1555-1564
    JournalJournal of Chemical Technology and Biotechnology
    Publication statusPublished - 1 Dec 2011


    • Fluidized bed
    • Hybridoma
    • Mammalian cell culture
    • Microencapsulation
    • Monoclonal antibodies
    • Perfusion processes

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