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High density and scale-up cultivation of recombinant CHO cell line and hybridomas with porous microcarrier Cytopore

机译:带有多孔微载体细胞孔的重组CHO细胞系和杂交瘤的高密度大规模培养

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摘要

Using porous microcarrier Cytopore and a low-serum medium supplement BIGBEF-3, we have successfully cultivated recombinant CHO cell line CL-11G producing prourokinase and hybridomas producing anti-prourokinase monoclonal antibody in Celligen 1.5 or 5 L bioreactor. The cell density obtained ranged from 1 to 2 × 107 cells mL-1. The yields of prourokinase and monoclonal antibody increased with increasing cell density. As the cells could spontaneously release from and reattach to porous microcarriers, it was very easy to scale-up the cultivation. Thus the bead to bead cell transfer method has been used to scale up the cultivation of CL-11G cells to a 20 L reactor-scale for the pilot production of prourokinase, and also to scale-up the culture of hybridomas for the production of monoclonal antibody for the purification of prourokinase.
机译:使用多孔微载体细胞孔和低血清培养基补充剂BIGBEF-3,我们已经成功地在Celligen 1.5或5 L生物反应器中培养了产生原尿激酶的重组CHO细胞系CL-11G和产生抗原尿激酶单克隆抗体的杂交瘤。获得的细胞密度范围为1至2×107细胞mL-1。尿激酶原和单克隆抗体的产量随细胞密度的增加而增加。由于细胞可以自发释放并重新附着在多孔微载体上,因此很容易扩大培养规模。因此,珠粒到珠粒细胞的转移方法已被用于将CL-11G细胞的培养规模扩大到20 L反应器规模,以试生产原尿激酶,还用于扩大杂交瘤的培养规模以生产单克隆抗体。用于纯化尿激酶的抗体。

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