Device and method for rabies virus inactivation and inactivator hydrolysis by virtue of disposable bags
A rabies virus and virus inactivation technology, which is applied in the direction of viruses, virus/bacteriophage, biochemical cleaning equipment, etc., can solve the problems of insufficient inactivation, antigen loss, etc., to reduce the risk of material splashing, damage, and reduce The effect of production costs
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Embodiment 1
[0040] Embodiment 1 Large-scale inactivation method of rabies vaccine virus liquid
[0041] Take the prepared Vero cell rabies virus harvest liquid and filter it through 0.8μm and 0.45μm microporous filters. After clarification and filtration, use Millipore's 300KD ultrafiltration membrane bag for ultrafiltration. The washing liquid (BME liquid, containing 0.02% glutamine by mass percentage, 24.63% sodium bicarbonate) is used to balance the membrane package, and the pH value of the reflux liquid is detected, and the pH value is 6.0. After meeting the requirements, it is concentrated, and the concentration ratio is 25 times. Transfer the virus pool from Port A to a disposable bag for inactivation. First dilute β-propiolactone with sterile water for injection 1:40 times, and then add it to the concentrated virus solution from port B of the bag according to the volume ratio of 1:100, and use PBS solution to wash from port B. Close the EZD valve 8, place it in a cold storage at 2...
Embodiment 2
[0042] Example 2 Hydrolysis of inactivator
[0043] The hydrolysis of β-propiolactone at 37°C was monitored by gas chromatography analysis method. Analysis of hydrolysis of β-propiolactone. Through the analysis of the test results, the concentration of β-propiolactone dropped from 299.4ppm when it was not hydrolyzed to 34.4ppm when it was hydrolyzed for 150min, which was lower than the quantitative limit of the method, indicating that β-propiolactone could be completely hydrolyzed at 37°C for 150min. hydrolysis effect.
Embodiment 3
[0044] Embodiment 3 cell method verification inactivation effect
[0045] According to the inactivation method of the embodiment, take the virus stock solution according to the ratio of inoculating 1ml per 3cm2 cells, inoculate the inactivated rabies virus solution on MRC-5 cells, culture for 7 days and then subculture, continue to cultivate until 21 days, and inoculate the cell suspension into Lab -tek chamber slides (purchased from Thermo Company), after 3-4 days, use immunofluorescence method on Lab-tek to observe whether there is rabies virus. Among them, the cell maintenance solution (MEM solution containing 4% fetal bovine serum) was replaced on the 14th day and 21st day respectively, and the cell supernatant was collected for mouse brain cavity poisoning, and the mice were observed for 21 days. A cell negative control and a virus positive control were also set up in the experiment to determine the validity of the experiment.
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