HIGH CELL-DENSITY PERFUSION CULTURES OF ANCHORAGE-DEPENDENT VERO CELLS IN A DEPTH FILTER PERFUSION SYSTEM

被引:9
|
作者
CHOI, SK
CHANG, HN
LEE, GM
KIM, IH
OH, DJ
机构
[1] KOREA ADV INST SCI & TECHNOL, DEPT CHEM ENGN, TAEJON 305701, SOUTH KOREA
[2] KOREA ADV INST SCI & TECHNOL, BIOPROC ENGN RES CTR, TAEJON 305701, SOUTH KOREA
[3] KOREA ADV INST SCI & TECHNOL, DEPT BIOTECHNOL, TAEJON 305701, SOUTH KOREA
[4] KIST, GENET ENGN RES INST, TAEJON 305600, SOUTH KOREA
[5] CHEIL FOODS & CHEM INC, CTR RES & DEV, KYONGGI DO 467810, SOUTH KOREA
关键词
DEPTH FILTER PERFUSION SYSTEM; VERO CELL CULTURE; GELATIN COATING; POLYPROPYLENE FIBER; AIR SPARGING; HIGH CELL DENSITY CULTURE;
D O I
10.1007/BF00749655
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A depth filter perfusion system (DFPS) with polypropylene fibers had been demonstrated to support high density cultures of anchorage-independent hybridoma cells. The DFPS provides advantages of high surface-to-volume ratio of 450-600 cm(2)/cm(3), low cost set-up, easy operation and scale-up. To test the feasibility of using DFPS for high density cultures of anchorage-dependent cells, Vero cells were cultivated in the DFPS. Gelatin coating on polypropylene fibers in the DFPS was necessary to promote cell attachment and growth. Dissolved oxygen (DO) concentrations could be controlled by sparging air into the reservoir vessel through a filter sparger. When DO concentration was controlled above 40% of air saturation in the DFPS with 40 mu m pore size, the maximum cell concentration as estimated on specific lactate production rate, was 3.81 x 10(7) cells/ml of the total reactor volume. This viable cell concentration is approximately 18 times higher than that obtained in a T-flask batch culture. Taken together, the results obtained here showed the potential of DFPS for high-density cultures of anchorage-dependent cells.
引用
收藏
页码:173 / 183
页数:11
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