Purification technology applicable to mass production of human-used avian influenza vaccine
A technology for avian influenza and avian influenza virus, applied in the direction of recovery/purification, medical preparations containing active ingredients, antibody medical ingredients, etc., can solve problems such as being easily affected by other conditions, uneven separation effects, and large batch-to-batch differences. Achieve the effect of low cost, small difference between batches, and simple process
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[0032] 1. Materials and equipment
[0033] Viral allantoic fluid batch number: Q0601 Q0602 Q0603 Q0604
[0034] Liquid volume (L): 34.0 35.2 35.5 35.2
[0035] Hemagglutination titer: 1:1280 1:960 1:1280 1:1280
[0036] pH7.2PBS
[0037] 30% and 55% sucrose
[0038] 300 mesh filter cloth
[0039] Continuous flow centrifuge: model CR21G (Hitachi)
[0040] Ultrafiltration concentration system: 100KD membrane bag Millipore company
[0041] Ultracentrifuge: Model CP70MX Hitachi Corporation
[0042] Ultraviolet detector: model 8823A-UL, peristaltic pump.
[0043] 2. Method
[0044] Four batches of viral allantoic fluid with batch numbers Q0601, Q0602, Q0603, and Q0604 were filtered with 300-mesh filter cloth to remove insoluble impurities such as egg skin, and then centrifuged at 8000rpm in a continuous flow centrifuge to remove macromolecular substances. The virus liquid was concentrated 30-50 times by 100KD membrane ultrafilter, and then centrifuged at 30,000 rpm for 3 h...
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