Application of VER-49009 in preparation of medicine for preventing and/or treating adenovirus infection
1. VER-49009, adenovirus technology, applied in the field of medicine, can solve problems such as undiscovered adenovirus infection, achieve broad application prospects, and inhibit replication
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Example 1: Evaluation of Cytotoxicity of VER-49009 in Vero Cell Lines
[0039] 1. Cell culture
[0040] After 2 passages of cryopreserved and resuscitated cells, use DMEM medium containing 10% fetal bovine serum and double antibody (penicillin 100U / mL, streptomycin 100μg / mL) for expansion and culture, and the seeding density is not less than 1 ×10 4 cell / mL, passage density not higher than 5×10 4 cells / mL.
[0041] 2. Drug treatment of cells
[0042] Vero cells by 1 x 10 4 Cells / well (volume 100 μL) were seeded in 96-well cell culture plates, and cultured for 24 hours until the confluence of cell wells reached 80%; 200 μL of culture medium (DMEM medium + 2% serum + double antibody) was used in each well to prepare drugs, and Add to the corresponding cell wells and mix. In the drug treatment group, 8 drug concentration gradients were set, and each gradient concentration was set up with 2 duplicate wells, and the final concentrations were 0.002 μM, 0.007 μM, 0.02 μM...
Embodiment 2
[0047] Example 2: Evaluation of anti-AdV3 adenovirus activity of VER-49009 in Vero cell line
[0048] 1. Cell culture
[0049] After 2 passages of cryopreserved and resuscitated cells, use DMEM medium containing 10% fetal bovine serum and double antibody (penicillin 100U / mL, streptomycin 100μg / mL) for expansion and culture, and the seeding density is not less than 1 ×10 4 cell / mL, passage density not higher than 5×10 4 cells / mL.
[0050] 2. Drug treatment of cells
[0051] Vero cells by 1 x 10 4 Cells / well (volume 100 μL) were inoculated in 96-well cell culture plates, and cultured for 24 hours until the confluence of cell wells reached 80%; AdV3 virus at 0.55 MOI (multiplicity of infection) was added to both the drug-treated group and the virus control group, while the drug-treated group Add each gradient concentration of the drug (with 5 μM as the starting concentration, 8 gradients of serial 3-fold serial dilution, two duplicate wells for each gradient) to a total volu...
Embodiment 3
[0061] Example 3: Evaluation of anti-AdV5 adenovirus activity of VER-49009 in Vero cell lines
[0062] 1. Cell culture
[0063] After 2 passages of cryopreserved and resuscitated cells, use DMEM medium containing 10% fetal bovine serum and double antibody (penicillin 100U / mL, streptomycin 100μg / mL) for expansion and culture, and the seeding density is not less than 1 ×10 4 cell / mL, passage density not higher than 5×10 4 cells / mL.
[0064] 2. Drug treatment of cells
[0065] Vero cells by 1 x 10 4 Cells / well (volume 100 μL) were inoculated in 96-well cell culture plates, and cultured for 24 hours until the confluence of cell wells reached 80%; 1.1 MOI (multiplicity of infection) AdV5 virus was added to the drug-treated group and the virus control group, while the drug-treated group Add each gradient concentration of the drug (with 5 μM as the starting concentration, 8 gradients of serial 3-fold serial dilution, two duplicate wells for each gradient) to a total volume of 20...
PUM
Property | Measurement | Unit |
---|---|---|
Passage density | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com