Development of a serum free medium for HUMIRA® biosimilar by design of experiment approaches

Author:

Kimiz-Gebologlu Ilgin1ORCID,Saglam-Metiner Pelin1,Ozaslan Oznur12,Ayyildiz-Tamis Duygu34,Deliloglu-Gurhan Saime Ismet3,Gulce-Iz Sultan135ORCID

Affiliation:

1. Ege University, Graduate School of Natural and Applied Sciences , Department of Bioengineering , Bornova/Izmir , Turkey

2. ILKO Ilac A.S., ARGEM Biotechnology R&D Center , Istanbul , Turkey

3. Ege University Faculty of Engineering , Department of Bioengineering , Bornova/Izmir , Turkey

4. Turgut Ilaclari A.S., Biotechnology Group , Process Development , Istanbul , Turkey

5. Ege University, Graduate School of Natural and Applied Sciences , Department of Biomedical Technologies , Bornova/Izmir , Turkey , e-mail:

Abstract

Abstract Background Serum have been traditionally used to support growth of animal cell cultures. However, the increasing growth of therapeutic biopharmaceuticals market, accelerated the high demand for the serum-free medium (SFM). Objective The main objective is to design a SFM for a stable rCHO cell line that produces a fully anti-human TNF-α monoclonal antibody (mAb) corresponding to HUMIRA® biosimilar. Materials and methods Design of Experiment (DoE) approaches were used to determine the key factors due to their effect on specific growth rate and mAb production. The production was carried out in T-flasks at different initial cell concentrations and then in Erlenmeyers with the developed SFM. mAb production was compared with commercial SFMs in terms of yield and productivity. Results Regarding to our findings, when the developed SFM-adapted cells were compared with the cells produced in commercial SFMs, the mAb productivity in developed SFM were higher (1.3–1.6 times) depending on higher mAb concentration and less (3–5 times) cell concentration. Additionally, the produced mAb in the developed SFM provided high conformational similarity with its originator HUMIRA®. Conclusion DoE approaches could be used to reduce cost and time in designing SFM for any commercially important cell line to produce high value biologics.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,Molecular Biology,Biochemistry

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