MONOCLONAL-ANTIBODY PROCESS-DEVELOPMENT USING MEDIUM CONCENTRATES

被引:68
作者
BIBILA, TA
RANUCCI, CS
GLAZOMITSKY, K
BUCKLAND, BC
AUNINS, JG
机构
[1] Bioprocess R&D Department, Merck Research Laboratories, Rahway, New Jersey
关键词
D O I
10.1021/bp00025a011
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 fed-batch process using concentrated medium was evaluated for its ability to improve cell culture longevity and final monoclonal antibody (MAb) titers for two monoclonal antibody producing cell lines. It was found to result in up to 7-fold increases in final antibody titers compared to batch culture controls. Although the development of cell line specific fed-batch protocols is critical to the development of cost-efficient large-scale production processes, the use of complete medium concentrates provided us with a quick and simple method for producing large quantities of antibodies in the early stages of process development, thus accelerating early work on purification process development, analytical development, biochemical characterization, and safety studies. Insights gained from the concentrated medium fed-batch approach were valuable for the development of refined, cell line specific feeding strategies yielding final MAb titers on the order of 1-2 g/L. Process development data on the effects of inhibitory growth byproducts, medium osmolarity, and the mode of nutrient feed addition on culture longevity and MAb production and information on culture metabolic behavior were successfully incorporated in the development of the optimized fed-batch protocols.
引用
收藏
页码:87 / 96
页数:10
相关论文
共 23 条
  • [1] MECHANISMS AND KINETICS OF MONOCLONAL-ANTIBODY SYNTHESIS AND SECRETION IN SYNCHRONOUS AND ASYNCHRONOUS HYBRIDOMA CELL-CULTURES
    ALRUBEAI, M
    EMERY, AN
    [J]. JOURNAL OF BIOTECHNOLOGY, 1990, 16 (1-2) : 67 - 86
  • [2] HIGH-LEVEL EXPRESSION OF A RECOMBINANT ANTIBODY FROM MYELOMA CELLS USING A GLUTAMINE-SYNTHETASE GENE AS AN AMPLIFIABLE SELECTABLE MARKER
    BEBBINGTON, CR
    RENNER, G
    THOMSON, S
    KING, D
    ABRAMS, D
    YARRANTON, GT
    [J]. BIO-TECHNOLOGY, 1992, 10 (02): : 169 - 175
  • [3] BIBILA T, 1993, 8 BIOCH ENG ENG F M
  • [4] BIBILA T, 1993, 205TH NAT M AM CHEM
  • [5] DETREMBLAY M, 1993, BIOPROCESS ENG, V9, P13
  • [6] DETREMBLAY M, 1992, BIOPROCESS ENG, V7, P229
  • [7] MATHEMATICAL DESCRIPTIONS OF HYBRIDOMA CULTURE KINETICS .3. SIMULATION OF FED-BATCH BIOREACTORS
    GLACKEN, MW
    HUANG, C
    SINSKEY, AJ
    [J]. JOURNAL OF BIOTECHNOLOGY, 1989, 10 (01) : 39 - 65
  • [8] GOULD S, 1992, IN VITRO CELL DEV 2, V3, pA162
  • [9] HETTWER DJ, 1991, AM I CHEM ENG ANN M
  • [10] QUANTITATIVE HPLC ANALYSIS OF PLASMA AMINO-ACIDS AS ORTHOPHTHALDIALDEHYDE ETHANETHIOL DERIVATIVES
    HILL, D
    BURNWORTH, L
    SKEA, W
    PFEIFER, R
    [J]. JOURNAL OF LIQUID CHROMATOGRAPHY, 1982, 5 (12): : 2369 - 2393