Abstract
Production of large quantities of diploid human fibroblasts in small culture volumes can be achieved using microcarrier culture techniques. Modification of the microcarrier culture procedure to include a virtually static attachment period and a reduced culture volume during the first 6 hr of culture was shown to double the attachment efficiency of the cells, improve the culture growth rate and increase final cell yields. Using the modified culture procedure yields greater than 2 × 106 cells/ml could be regularly obtained when 7–8 viable cells/microcarrier were used to inoculate a culture containing 3 mg of Cytodex® 1 microcarriers/ml. A protocol for the mass production of human beta interferon from microcarrier cultures is described. After priming the culture with beta interferon the superinduction step involves use of a poly (I) · poly(C)/DEAE-Dextran complex. Modifications to the microcarrier culture procedure and to the interferon production sequence enable the production of 3 × 108 IU of interferon from a 5 liter microcarrier culture of human fibroblasts. This quantity of interferon corresponds to a yield of approximately 30 IU/103 cells or 2 × 104 IU/mg of microcarrier.
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