Respiratory syncytial virosome vaccine and preparation method thereof
A syncytial virus, respiratory technology, used in antiviral agents, pharmaceutical formulations, antibody medical ingredients, etc.
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Embodiment 1
[0044] Example 1: Screening and Determination of Respiratory Syncytial Virus Vaccine Strains
[0045] Clinical throat swab samples of respiratory tract infection were collected from 20 provinces and cities CDC in different regions of my country, east, west, north, south, middle, and the RSV virus was amplified and purified by cell culture for vaccine production. Tests such as biology, virus titration and exogenous factors, etc., to screen candidate dominant vaccine virus strains. Further prepare the immune serum of candidate dominant vaccine virus strains, and carry out immunization with clinically isolated RSV epidemic wild strains in different regions in recent years, purchased A-type RSV A2 standard strains, B-type G8537 standard strains, and RSV clinically isolated strains preserved by China CDC and China Inspection Institute. Cross-neutralization studies, the results show that the immunoneutralization crossover between the identified candidate RSV type A and B vaccine stra...
Embodiment 2
[0046] Example 2: Cell culture and cell batch bank establishment
[0047] Take human diploid cells (2BS Cell) as an example: 2BS cells come from American Type Culture Collection (ATCC). The culture medium adopts Dulbecco's modified Eagle medium (DMEM), adds gentamicin, does not add or adds a certain amount of fetal calf serum (2-10%) to cultivate in cell factory or cell fermenter, establishes cell work seed batch library, and And the foreign aid source factors, tumorigenicity and stability after passage are comprehensively tested, and the number of cell generations used is controlled within 40 generations, which all meet the requirements of vaccine production media.
[0048] The cell culture and cell batch bank establishment can be one of the following cells: ① human diploid cells; ② ELL-0 cells; ③ Vero cells; ④ CHO cells; ⑤ Hep-2 cells; ⑥ MDCK cells.
Embodiment 3
[0049] Example 3: Large-scale production and purification of RSV culture and proliferation
[0050] ① RSV was inoculated in human diploid cells (2BS) cells covering the bottom of the flask, cultured at 37°C for 48 hours, collected cells, and centrifuged at 5000rmp at 4°C for 5 minutes to remove cells and impurities. ②The supernatant was taken and subjected to sucrose gradient centrifugation. The sucrose was prepared with PBS buffer, and the system used 4 mL of 30% sucrose; 4 mL of 45% sucrose; 1 mL of 60% sucrose. Centrifuge at 100000g for 2h at 4°C. ③ Aspirate 30% and 40% interlayers, add an appropriate amount of PBS to dilute, and continue ultracentrifugation at 100,000 g at 4°C for 2 hours. ④ Collect the precipitate and measure the density with a refractometer. Store in RSV preservation solution (17.4% Glycerol, 145mM NaCl, 2.5mM HEPES, 0.1mM MgCl2, 0.1mM CaCl2, pH 7.4) for later use. The RSV includes A subtype and B subtype.
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