Method for industrially producing porcine Japanese encephalitis (JE) vaccines by utilizing bioreactor
A bioreactor, porcine encephalitis technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of unreported production methods of porcine encephalitis vaccine, unstable product quality, and intensive manual operations and other issues to achieve the effect of saving manpower, small differences between batches, and reducing costs
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Embodiment 1
[0022] Bioreactor: 14L and 40L bioreactors from NBS Company of the United States;
[0023] Microcarrier: Cytodex-1 (General Electric Healthcare Life Sciences Division);
[0024] Porcine encephalitis virus: HW1 strain;
[0025] Cell growth medium: M199 (Beijing Qingda Tianyi Biotechnology Co., Ltd.) containing 8% calf serum by volume;
[0026] Virus maintenance solution: M199 (Beijing Qingda Tianyi Biotechnology Co., Ltd.) containing 1% calf serum by volume;
[0027] Cell culture: In 14L bioreactors, add Cytodex1 at a concentration of 10g / L. After hydration, wash with pH 7.2 phosphate buffered saline PBS twice, sterilize, add cell growth medium to balance, and inoculate Vero The cells were cultured; the parameters of the culture method were: pH 7.2, temperature 37°C, dissolved oxygen 50%, stirring speed 30-100rpm; samples were taken regularly every day to observe the growth of the cells, and the cells were counted to determine the consumption of glucose. Density up to 1.5×10...
Embodiment 2
[0032] Bioreactor: 14L and 40L bioreactors from NBS Company of the United States;
[0033] Microcarrier: Cytodex-1 (General Electric Healthcare Life Sciences Division);
[0034] Porcine encephalitis virus: HW1 strain;
[0035] Cell growth medium: M199 (Beijing Qingda Tianyi Biotechnology Co., Ltd.) containing 8% calf serum by volume;
[0036] Virus maintenance solution: M199 (Beijing Qingda Tianyi Biotechnology Co., Ltd.) containing 1% calf serum by volume;
[0037] Cell culture: In 14L bioreactors, add Cytodex1 at a concentration of 10g / L, after hydration, wash with pH 7.2 phosphate buffer saline PBS twice, sterilize, add cell growth solution to balance, and inoculate BHK -21 cells were cultured; the parameters of the culture method were: pH 7.2, temperature 37°C, dissolved oxygen 50%, stirring speed 30-100rpm; samples were taken regularly every day to observe the growth of the cells, and the cells were counted to determine the consumption of glucose. The density of the ce...
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