Grachev V P, Zaval'nyĭ M A, Popova V D, Khanina M K, Mironova L L
Vopr Virusol. 1983 Jul-Aug;28(4):44-9.
The paper presents the results of experiments on propagation of primary, secondary, and continuous diploid and heteroploid human and animal cells in 2 different systems for large-scale propagation: in perfusion tank with Rashig rings and in tanks with microcarriers. Both methods of large-scale cultivation produce higher cell yields than the traditional cultivation methods. A yield of tick-borne encephalitis virus per 1 cell in the perfusion cultivator was 12 times as high as in roller cultures. Poliomyelitis virus titres were practically equal with both methods of large-scale cultivation and with the conventional method (7.73 lg PFU/ml in GMKC on microcarriers). The method of cultivation on microcarriers is more acceptable and advantageous as it gives higher yields of cells necessary for growth of poliomyelitis virus.
本文介绍了在两种不同的大规模培养系统中,即装有拉西环的灌注罐和装有微载体的罐中,对原代、传代以及连续二倍体和异倍体人及动物细胞进行培养的实验结果。这两种大规模培养方法均比传统培养方法产生更高的细胞产量。在灌注培养器中,每1个细胞产生的蜱传脑炎病毒产量比滚瓶培养高12倍。两种大规模培养方法以及传统方法培养的脊髓灰质炎病毒滴度实际上相当(在微载体上的GMKC中为7.73 lg PFU/ml)。微载体培养方法更易于接受且具有优势,因为它能产生更高产量的脊髓灰质炎病毒生长所需细胞。