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Recombinant Antibody Production by Perfusion Cultures of rCHO Cells in a Depth Filter Perfusion System

机译:在深度过滤器灌注系统中通过rCHO细胞灌注培养产生重组抗体

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摘要

Recombinant Chinese hamster ovary cells,producing recombinant antibody against the human platelet,were cultivated in a depth filter perfusion system (DFPS).When perfusion cultures with working volume of 1 L were operated at perfusion rates of 5/d and 6/d,volumetric antibody productivities reached values 28 and 34 times higher than that of batch suspension culture in Erlenmeyer flasks and 43 and 53 times higher than that of batch culture in a controlled stirred tank reactor,respectively.Perfusion cultures in the DFPS showed stable antibody production over the whole culture period of up to 20 days.In the DFPS,inoculated cells in suspension were entrapped in a few hours within the depth filter matrix by medium circulation and retained there until the void space of the filter matrix was saturated by the cultured cells.After cells in the depth filter matrix reached saturation,overgrown viable cells at a perfusion rate of 5/d or 6/d were continuously collected into waste medium at a density of 2-4 x 10~5 cells/mL,which resulted in stable operation at high perfusion rates,maintaining values of process parameters such as glucose/lactate concentration,pH,and dissolved oxygen concentration.Because the DFPS overcomes most drawbacks observed with conventional perfusion systems,it is preferable to be used as a key culture system to produce monoclonal antibody stably for a long culture period.
机译:在深度过滤器灌注系统(DFPS)中培养产生重组抗人血小板抗体的中国仓鼠卵巢细胞。当以5 / d和6 / d的灌注速率操作体积为1 L的灌注培养物时抗体的产量分别达到锥形瓶中悬浮培养的28倍和34倍,比受控搅拌釜反应器中的批次培养分别高出43倍和53倍.DFPS中的灌注培养在整个过程中显示出稳定的抗体产量培养时间长达20天。在DFPS中,悬浮液中的接种细胞通过培养基循环在深层过滤器基质中滞留数小时,并保留在那里,直到培养的细胞使过滤器基质的空隙空间饱和为止。在深度过滤器基质中达到饱和后,以5 / d或6 / d的灌注速率将生长过度的活细胞以一定密度连续收集到废液中2-4 x 10〜5细胞/ mL,可在高灌注速率下稳定运行,保持葡萄糖/乳酸浓度,pH和溶解氧浓度等工艺参数值。因为DFPS克服了传统方法中观察到的大多数缺点灌注系统,优选用作关键培养系统,以在长时间培养中稳定产生单克隆抗体。

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