The factors which limit the proliferation of eukaryotic cells in vitro
are still not well known. Ammonia is believed to be toxic for mammali
an cell proliferation and secretion. We have tried two approaches to r
educing the ammonia in the medium. We first limited the ammonia produc
ed by the cells by replacing glutamine by glutamate. Then, we used two
chemical engineering methods to eliminate accumulated ammonia. In one
the used medium was passed through a natural cation exchanger: the cl
inoptilolite. In the other, the culture medium was passed through a hy
drophobic microporous hollow fiber module. Replacing the glutamine by
glutamate reduced the medium ammonia concentration. The physicochemica
l removal of ammonia induced a better cell growth, but not a better sp
ecific antibody secretion.