A method for continuous large-scale production of recombinant adenovirus
A recombinant adenovirus, a large-scale technology, applied in the direction of supporting/immobilizing microorganisms, biochemical equipment and methods, viruses, etc., can solve the problems of poor cycle and poor relative stability of cells, achieve low cost and improve cell growth environment , the effect of small shear force
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Embodiment 1
[0059] A method for continuous large-scale production of recombinant adenovirus provided in this embodiment comprises the following steps:
[0060] Step 1. Cell Culture
[0061] 1) Cell recovery: Take a HEK293 cell cryopreservation tube and put it in warm water at 37°C for instant dissolution, and take it out immediately when only a small ice core remains, wipe the surface of the cryopreservation tube with a 70%-75% alcohol cotton ball After disinfection, open the cap of the tube on the ultra-clean workbench, aspirate the cell suspension with a 5ml pipette and gently pour it into a sterile centrifuge tube containing DMEM medium, and mix gently; freeze the cells with a 5ml pipette. The stored solution was sucked into a 15ml centrifuge tube, centrifuged (800 rpm for 4 minutes), the supernatant was discarded, and DMEM medium was added to resuspend the cells; the resuspended cells were added to the square flask (sampling, counting) , cultured in an incubator, incubator conditions...
Embodiment 2
[0074] This example is similar to the experimental steps used in the method for continuous large-scale production of recombinant adeno-associated virus described in Example 1, except that:
[0075] The carrier filling number in the cell culture bag in steps 2 and 3 is 10g / L;
[0076] In steps 2 and 3, the cell seeding density is 1E+5 cells / ml;
[0077] In step 2, the daily sugar consumption of the cells in the 3L cell culture bag is 4.0±0.5g. When the cells are expanded and cultured, part of the cells are left in the 3L cell culture bag for culture, and part is inoculated into the 30L cell culture bag for enlarged culture;
[0078] In step 3, when the cells in the 30L cell culture bag are inoculated with adenovirus, the daily sugar consumption is 40±5g, and the total number of cells is 5.3E+10; the MOI of virus-infected host cells is 20; the total number of virus particles is 1.3E+15 ; The cell yield is about 2.45E+4.
Embodiment 3
[0080] This example is similar to the method for continuous large-scale production of recombinant adeno-associated virus described in Example 1, except that:
[0081] The carrier filling number in the cell culture bag in step 2 and step 3 is 40g / L;
[0082] In step 2 and step 3, the number of cell inoculations is 4E+5 / ml;
[0083] In step 2, the daily sugar consumption of the cells in the 3L cell culture bag is 9.0±0.5g. When the cells are expanded and cultured, part of the cells are left in the 3L cell culture bag for culture, and part is inoculated into the 30L cell culture bag for enlarged culture;
[0084] In step 3, when the cells in the 30L cell culture bag are inoculated with adenovirus, the daily sugar consumption is 90.0±5g, and the total number of cells is 1.26E+11; the MOI of virus-infected host cells is 20; the total number of virus particles is 2.65E+15 ; The cell yield is about 2.10E+4.
[0085] The purity of the recombinant adenovirus products obtained in Exam...
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