Method for screening anti-aids drug
A screening method and anti-AIDS technology, applied in the field of molecular biology, can solve problems such as cost constraints, and achieve the effect of accurate drug efficacy
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Embodiment 1, the selection of optimal cell ratio and optimal co-culture conditions
[0032] (1) Normal cell culture (that is, the cells can grow normally) JLTRG cells and H9 cells are cultured using 1640 medium containing 10% FBS, 1% streptomycin and 1% penicillin (that is, adding 100g per liter of 1640 medium FBS of 10g, streptomycin of 10g and penicillin of 10g), cell count; Generally, the number of suspension in every 2ml of 1640 culture medium containing 10% FBS, 1% streptomycin and 1% penicillin is 10 6 Cell. Cultured in a cell culture incubator at 37°C with CO 2 The concentration (volume concentration) is 5%, and the humidity (relative humidity) is 75%. The incubation time is generally 24 hours.
[0033] (2) Put JLTRG cells and H9 cells in 5% FBS, 1% streptomycin and 1% Penicillin 1640 medium co-cultured for 24 hours, 48 hours, 72 hours, 96 hours. Cultured in a cell culture incubator at 37°C with CO 2 The concentration is 5% and the humidity is 75%. The nu...
Embodiment 2
[0039] Embodiment 2, take three kinds of existing medicines (T20, EFV, PTD) as experimental detection target, determine the practicability of the method of the present invention:
[0040] According to the experimental conditions screened above, JLTRG cells and H9 cells were co-cultured in 1640 medium with 5% FBS, 1% streptomycin and 1% penicillin at a cell ratio of 10:1.
[0041] (1) Dilute different drugs, T20 (0.00015uM, 0.0006uM, 0.3uM, 0.003uM, 0.015uM, 0.06uM),
[0042] PTD (1.5uM.0.75uM, 0.375uM, 0.18, 0.09, 0.045uM),
[0043] EFV (0.6uM, 0.15um, 0.03uM, 0.006uM, 0.0015, 0.0003uM);
[0044] Both use RPMI 1640 medium as the diluent.
[0045] (2) Cultivate the above-mentioned three types of drug solutions with different concentrations and JLTRG cells for 6 hours. The number of each hole is 10 6 The JLTRG cells were cultivated in a cell culture incubator at 37°C, and the CO in the cell culture incubator 2 The concentration is 5%, the humidity is 75%; the tending time i...
PUM
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