Mouse hybridoma cells were succesfully cultivated for more than 640 hours in the interparticle spaces of a tubular reactor packed with spherical dass beads. The maximum monoclonal antibody (MAb) concentration attained was 110 mg/l and a viable cell density in the order of 1 X 1 O7 cells/ml was achie
An immobilized hybridoma culture perfusion system for production of monoclonal antibodies
β Scribed by Arye Lazar; Lea Silberstein; Avshalom Mizrahi; Shaul Reuveny
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 456 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0920-9069
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β¦ Synopsis
A fixed bed perfusion system for hybridoma cell immobilization is presented. The system consists of a culturing vessel (300 ml total volume) in which polyurethane (PU) sponges in the form of small cubes of about 5 mm sides are packed. Cells are immobilized by physical entrapment in the foam matrix. By entrapment of the cells in the pores of the matrix high cell concentration can be maintained in a mechanically protected environment. Medium is continuously circulated by an airlift pump mounted in the cell-free chamber (700 ml total volume).
Medium flow rate, feeding rate, dissolved oxygen, pH, nutrient uptake and waste product formation can be easily monitored and controlled. Steady state conditions are established with medium dilution rates of 1.0-1.5 reactor volume per day. The steady state is characterized by a constant cell density, constant culture volume and constant glucose and lactate levels. Cell-free supernatant is collected continuously in a cold room adjacent to the 37~ culture room. Monoclonal antibodies (MAb) are produced at a concentration of 150-200 lxg/ml for several weeks. An important feature of the system is the capacity to maintain a population of cells after the growth phase in a non-proliferating state for extended time periods expressing high titers of MAb.
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## Abstract The flowβcytometric (FCM) analysis of bivariate DNA/lgG distributions has been conducted to study the cell cycle kinetics and monoclonal antibody (MAb) production during perfusion culture of hybridoma cells. Three different perfusion rates were employed to demonstrate the dependency of
To determine the effect of hyperosmotic stress on the monoclonal antibody (MAb) production by calciumalginate-immobilized S3H5iy2bA2 hybridoma cells, the osmolalities of medium in the M A b production stage were varied through the addition of NaCI. The specific MAb productivity (9Mab) of immobilized
## Abstract Cell proliferation and longβterm production of monoclonal antibody IgG~2b~ by M2139 hybridoma cells immobilized in macroporous gel particles (MGPs) in packedβbed reactor were studied for a period of 60 days. The MGPs were made of supermacroporous gels produced in frozen conditions from