Tokashiki M, Takamatsu H
Tokyo Research Center, Teijin Limited, Japan.
Cytotechnology. 1993;13(3):149-59. doi: 10.1007/BF00749811.
A variety of processes have been proposed for mammalian cell culture in the commercial production of useful substances (e.g., monoclonal antibodies, therapeutic and diagnostic proteins). Among them, the perfusion culture of suspended non-immobilized cells is the most advantageous. Perfusion culture can be classified by the separation process of suspended cells from the culture mixture into three types, namely filtration, gravitational settling and centrifugation. From a commercial point of view, the present situation and technical problems of suspended cell perfusion culture will be reviewed based on the three types. The recent development of perfusion culture has been carried out mainly on the filtration separation process, but the centrifugation process seems to have a promising future because of operation stability and scale-up feasibility. The reasons will be explained in details.
在有用物质(如单克隆抗体、治疗性和诊断性蛋白质)的商业生产中,已经提出了多种用于哺乳动物细胞培养的方法。其中,悬浮非固定化细胞的灌注培养是最具优势的。灌注培养可根据从培养混合物中分离悬浮细胞的过程分为三种类型,即过滤、重力沉降和离心。从商业角度来看,将基于这三种类型对悬浮细胞灌注培养的现状和技术问题进行综述。灌注培养的最新进展主要是在过滤分离过程方面,但离心过程由于操作稳定性和放大可行性似乎具有广阔的前景。将详细解释其原因。