A SIMPLE AND INEXPENSIVE HIGH-DENSITY DIALYSIS TUBING CELL-CULTURE SYSTEM FOR THE IN-VITRO PRODUCTION OF MONOCLONAL-ANTIBODIES IN HIGH-CONCENTRATION

被引:19
作者
FALKENBERG, FW
HENGELAGE, T
KRANE, M
BARTELS, I
ALBRECHT, A
HOLTMEIER, N
WUTHRICH, M
机构
[1] Abteilung für Medizinische Mikrobiologie und Immunologie, Institut für Hygiene und Mikrobiologie, Ruhr-Universität Bochum
关键词
MONOCLONAL ANTIBODY PRODUCTION; HIGH DENSITY HYBRIDOMA CULTURE; DIALYSIS BAG CULTURE;
D O I
10.1016/0022-1759(93)90345-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the construction and application of a low-cost roller bottle-like culture appliance in which hybridoma cells can be cultivated in high density in dialysis tubing. The appliance facilitates the simultaneous culture of up to four cell lines yielding 50 ml culture volume of each. Samples for follow-up analysis of the cultures can easily be taken when needed through sample ports. In order to obtain high cell densities (at least 10(7) cells/ml), high cell viability (at least 50%) and high antibody yield (at least 1.0 mg/ml) the bottle is rolled at a speed of 4-6 rpm and is gassed continuously by a micropump driven by rechargeable NiCd batteries fixed to the culture flask. Depending on the individual properties of the hybridoma lines tested, the cells may be cultured for 1-2 weeks, and cell densities of up to 30 x 10(6) cells/ml with viabilities of approximately 50% and monoclonal antibodies in concentrations of up to 2.8 mg/ml may be obtained. In their properties the monoclonal antibodies produced by this in vitro procedure are indistinguishable from those prepared in the form of conventional stationary culture supernatant or of ascitic fluid. Specific antibody content is within the same range as in ascitic fluid. Consequently, the monoclonal antibodies can be purified in one step, e.g., by ion exchange chromatography from the culture supernatant. Therefore. the newly developed culture device and the culture method described is a useful alternative to ascites production in live mice.
引用
收藏
页码:193 / 206
页数:14
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