Application of anti-human immunodeficiency virus (HIV) drug amprenavir in preparation of antitumor drug
A tumor and drug technology, applied in the field of medicine, can solve the problem that the inhibitory effect has not been reported, and achieve the effect of shortening the research and development cycle, inhibiting the proliferation of tumor cells, and reducing the research and development investment.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Embodiment 1: Preparation of amprenavir stock solution
[0043] Amprenavir (CAS No.161814-49-9, purity>98%) was purchased from Shanghai Hanxiang Biotechnology Co., Ltd. Drugs were first dissolved in DMSO to make a concentration of 10 -2 Stock solution of M, aliquoted, stored at -80°C
Embodiment 2
[0044] Embodiment 2: the culture of tumor cell
[0045] 1. Materials and methods
[0046] 1.1 Materials
[0047] Strains: breast cancer MCF-7 cells, non-small cell lung cancer A549 cells, mouse fibroblastoma L929 cells, colon cancer HT29 cells, glioma U87 cells (purchased from the cell bank of Shanghai Institute of Biological Sciences)
[0048] Medium: RPMI-1640 medium (100 M / mL penicillin + 100 M / mL streptomycin) supplemented with 10% (v / v) calf serum
[0049] 1.2 Method
[0050] (1) Cells were grown in suspension in RPMI-1640 medium (100 M / mL penicillin + 100 M / mL streptomycin) containing 10% calf serum, at 37°C, saturated humidity, 5% CO 2 cultured in an incubator.
[0051] (2) Change the culture medium once every 2-3 days.
[0052] (3) Collect the cells in the logarithmic growth phase for experiments.
Embodiment 3
[0053] Example 3: Inhibitory effect of Amprenavir on tumor cell proliferation
[0054] 1. Materials and methods
[0055] 1.1 Materials
[0056] 50 μM, 100 μM, 150 μM, 200 μM amprenavir solution: use the amprenavir stock solution obtained in Example 1 for dilution.
[0057] Breast cancer MCF-7 cells in logarithmic phase, non-small cell lung cancer A549 cells, mouse fibroblastoma L929 cells, colon cancer HT29 cells, and brain glioma U87 cells: obtained by the method described in Example 2.
[0058] 1.2 Method
[0059] (1) with 5×10 4 cells / mL, the tumor cells were inoculated in a 96-well plate, 100 μL of cell suspension per well (3 replicate wells for each group), and cultured for 24 hours.
[0060] (2) Using the RPMI-1640 culture medium without cells as the blank control group, add amprenavir at the final concentrations of 50, 100, 150, and 200 μM to the cultured cells, and culture them for 24h and 48h respectively.
[0061] (3) After adding 10 μL, 5 mg / mL MTT to each we...
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