Application of daurisoline in preparation of drugs to prevent and treat lung cancer
A technology of bat puerarin and lung cancer, applied in the field of medicine, can solve the problems of increasing the sensitivity of cancer cells, etc., and achieve the effects of good development and utilization, low price, and small toxic and side effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1W
[0018] Example 1 WST-1 cell activity detection
[0019] 1. Cell plating: collect A549 and Hop62 cells (both cells were purchased from ATCC), perform cell counting, spread in 96-well plates according to the amount of 3000 cells per well, and culture overnight.
[0020] 2. Drug treatment: dilute bat-guisurin with DMEM complete medium to the treatment concentration (0, 1.25, 2.5, 5, 10, 20 μM), then replace the original medium in the 96-well plate, and treat for 12, 24 and 48 hours respectively.
[0021] 3. WST-1 detection: according to the dilution ratio of 1:10 (w / v), dilute WST-1 (WST-1 cell proliferation detection kit) with DMEM complete medium to obtain the medium containing WST-1; then The medium containing WST-1 was used to replace the original medium in the 96-well plate, and the medium containing WST-1 was added to wells without cultured cells as a blank control, 100 μL per well. Then put the 96-well plate in a constant temperature incubator at 37°C and incubate for 1 h...
Embodiment 2
[0023] Embodiment 2 clone formation experiment
[0024] 1. Cell plating: collect A549 and Hop62 cells, perform cell counting, spread in 6-well plates according to the amount of 1000 cells per well, and culture overnight.
[0025] 2. Drug treatment: use DMEM complete medium to dilute bat Gesurin to a treatment concentration of 10 μM, then replace the original medium in the 6-well plate, 2 mL per well; at the same time, dilute DMSO (dimethyl sulfoxide) with DMEM complete medium ) to the treatment concentration (10 μM) as the control.
[0026] 3. After two weeks of drug treatment, observe the cell plate under the light to see if there are cloned dots visible to the naked eye.
[0027] 4. When visible cloning dots appear on the cell plate, remove the original medium, wash the remaining medium with PBS buffer, and repeat twice.
[0028] 5. Fixation: Add anhydrous methanol to the 6-well plate, shake the cell plate slowly, and fix at room temperature for 20 minutes.
[0029] 6. St...
Embodiment 3
[0032] Embodiment 3 subcutaneous tumor formation experiment in nude mice
[0033] 1. The animal experiments in this project strictly complied with the guidelines of animal care institutions, and all were approved by the Animal Experiment Ethics Committee of Jinan University.
[0034] 2. The experimental animals used in this project are 6-8 weeks old female nude mice (Balb / c-nu, Experimental Animal Center of Southern Medical University), a total of 15, including 5 in the control group and 10 in the experimental group. Mouse subcutaneous tumor model:
[0035] (1) Cell collection: collect cells for cell counting, and use 1×10 cells per nude mouse 6 The total number of cells was calculated based on the amount of A549 cells, and the cells were resuspended in PBS buffer and mixed with Matrigel (purchased from Guangzhou Sier Biotechnology Co., Ltd., coring) at a volume ratio of 1:1.
[0036] (2) Inoculation: after the mice were anesthetized (evaluate the degree of anesthesia throug...
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