摘要
用自制大孔明胶微载体与实心微载体CT-3在转瓶中培养Vero细胞,在培养后期许多细胞从CT-3上脱落下来,细胞密度降低,而大孔微载体上的细胞密度一直保持在较高水平(8×108cels/L以上),表明大孔微载体能够延长细胞活性期。用大孔明胶微载体在反应器中培养Vero细胞,最大活细胞密度达5.6×109cels/L。
With solid CT 3 microcarriers as a control, Vero cells on gelatin based macroporous microcarriers were cultivated in Wheaton spinner bottles. During first three days of cultivation, cell density on porous carriers was lower than that on CT 3. But at the late stage of cultivation, cell density on porous carriers kept a high level (above 8×10 8 cells/L), whereas cells on CT 3 began to detach. When cells were cultured in a 1.5L CelliGen bioreactor using gelatin based macroporous microcarriers, the viable cell density reached a maximum of 5.6×10 9cells/L.
出处
《华东理工大学学报(自然科学版)》
EI
CAS
CSCD
北大核心
1997年第4期417-421,共5页
Journal of East China University of Science and Technology
关键词
细胞培养
明胶
微载体
VERO细胞
cell culture
gelatin
microcarrier
macroporous microcarrier
Vero cells