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Hybridoma perfusion system using a sedimentation device
Authors:Thomas L. LaPorte  Jerry Shevitz  Youngsun Kim  Shaw S. Wang
Affiliation:(1) Department of Chemical and Biochemical Engineering, Rutgers, the State University of NJ, 08855 Piscataway, NJ, USA;(2) New Brunswick Scientific, 08818 Edison, NJ, USA;(3) Present address: Bristol-Myers Squibb Company, 08903 New Brunswick, NJ, USA;(4) Present address: Incell corporation, 07039 Livingston, NJ, USA
Abstract:Summary A novel sedimentation method with a spiral decanter was utilized with a bioreactor for propagation of hybridoma cells at high densities. The live cell concentration was increased and cell lysis was greatly reduced in this system compared to a tangential flow hollow fiber perfusion system. The specific monoclonal antibody productivity was higher than that obtained using a hollow fiber perfusion system or in a batch culture. Cell specific productivity usually declined over time in long term experiments. The use of the sedimentation device eliminated progressive deterioration of reactor performance usually associated with a perfusion device.
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