US2020093915A1PendingUtilityA1
Vaccine Containing Virus-Like Particles
Est. expiryJul 18, 2034(~8 yrs left)· nominal 20-yr term from priority
Inventors:Kazuhiko KimachiMotoharu AbeKazuyuki IkedaHiroto OnumaYukari TsurudomeDaisuke IkenoKiyoto NishiyamaTatsufumi OnchiYusuke OoyamaIssay AsanoRyoichi Kitano
A61K 39/12A61K 39/145A61K 39/29C12N 2760/16123C12N 7/00C12N 2760/16234C12N 2760/16134A61K 2039/5258C12N 2760/16223Y02A50/39A61K 2039/55572C12N 2770/24134C12N 2770/24123C12N 2760/16251C12N 2760/16151C12N 2730/10134C12N 2730/10123A61K 2039/55505Y02A50/30
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Claims
Abstract
The present invention provides a vaccine containing virus-like particles derived from virus particles having an envelope, in which a lipid-component content of the virus-like particles is reduced relative to a lipid-component content of the virus particles.
Claims
exact text as granted — not AI-modified1 .- 15 . (canceled)
16 . A method for manufacturing a vaccine containing virus-like particles, comprising:
fixing particle structures of virus particles having an envelope; and performing a delipidation treatment on the fixed virus particles.
17 . The manufacturing method according to claim 16 , wherein the fixing includes adding a fixative to a suspension A containing the virus particles.
18 . The manufacturing method according to claim 17 , wherein the fixative contains aldehydes.
19 . The manufacturing method according to claim 17 , wherein the fixative contains 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (EDC).
20 . The manufacturing method according to claim 18 , wherein the aldehydes are selected from the group consisting of formaldehyde, paraformaldehyde, glutaraldehyde, and a combination of these.
21 . The manufacturing method according to claim 20 , wherein the aldehydes contain formaldehyde.
22 . The manufacturing method according to claim 21 , wherein a concentration of the formaldehyde is 0.007 to 0.076 w/v % based on a total amount of the suspension A and the fixative.
23 . The manufacturing method according to claim 20 , wherein the aldehydes contain glutaraldehyde.
24 . The manufacturing method according to claim 23 , wherein a concentration of the glutaraldehyde is 0.002 to 0.05 w/v % based on a total amount of the suspension A and the fixative.
25 . The manufacturing method according to claim 16 , wherein the step of performing a delipidation treatment includes adding a delipidation agent to a suspension B containing the fixed virus particles.
26 . The manufacturing method according to claim 25 , wherein the delipidation agent is selected from the group consisting of diethyl ether, diisopropyl ether, methyl acetate, ethyl acetate, and a combination of these.
27 . The manufacturing method according to claim 26 , wherein the delipidation agent contains diethyl ether.
28 . The manufacturing method according to claim 27 , wherein a concentration of the diethyl ether is equal to or higher than 10 vol % based on a total amount of the suspension B and the delipidation agent.
29 . The manufacturing method according to claim 25 , wherein the delipidation agent further contains a surfactant.
30 . The manufacturing method according to claim 16 , wherein the virus particles are recovered after being caused to infect a culture cell or a chicken egg.
31 . The manufacturing method according to claim 30 , wherein the culture cell is a Vero cell or an MDCK cells.Join the waitlist — get patent alerts
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