Preparation method and usage of Asiatic toddalia root total alkaloid effective part extract
A technology of total alkaloids and effective parts is applied in the preparation of extracts from effective parts of total alkaloids in the blood of Fenugreek, and in the field of preparing anti-tumor drugs, which can solve the problems of cytotoxicity and tumor cell apoptosis in Fenugreek blood, and achieve inhibition of The economic effect of tumor cell proliferation and purification process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Weigh 50g of the pulverized Pterodactylus japonicus root, immerse in 70% ethanol for 12h, and then heat extract twice, each time the amount of solvent is 10 times, each extraction time is 2 hours, combine the two extracts, concentrate to a thick extract, Vacuum-dried to obtain the effective part extract of Feilongzhang Blood Alcohol Extraction of the present invention, weighing 5.091g, and the content of limpetine chloride measured by high performance liquid phase is 0.183mg.
Embodiment 2
[0040] Weigh 5 g of the pulverized blood root of Flying Dragon palm, impregnate it with 70% ethanol for 12 h, then heat extract 3 times, the amount of solvent is 10 times each time, and the extraction time is 60 min each time, combine the extracts for 3 times, concentrate until thick paste, use 1 mol / L hydrochloric acid to adjust the pH of the sample solution to 2, the concentration of the sample solution is 0.1 mg crude drug / ml, pass through 30 ml D001 type cation-exchange macroporous resin at a flow rate of 1.5 BV / h, and successively wash with 500 ml water Impurities were removed by elution, and then eluted with about 300 ml of 95% ethanol-ammonia water (9:1), the eluate was collected, concentrated to a thick extract, and dried in vacuum to obtain the effective position extract, the content of total alkaloids in the extract from the three batches of samples is shown in Table 1,
[0041] Table 1 Validation of extraction and purification process
[0042] serial numb...
Embodiment 3
[0044] In vitro inhibition of the proliferation of human tumor cells A549, AGS, SGC-7901, SMMC-7721, the tumor cells fused into a monolayer were digested with 0.25% trypsin, counted and adjusted to a cell concentration of 5×10 4 cells / mL, inoculated in 96-well plate, 90 μL / well, set negative control group, positive control group and blank control group (only culture medium, no cells and drugs) at the same time, placed in 37 ℃, 5% CO 2 After culturing in the incubator for 24 hours, 10 μL of test sample solution of different concentrations were added to the experimental group, 10 μL of 5-fluorouracil (5-Fu) solution of different concentrations were added to the positive control group, and 10 μL of 5-fluorouracil (5-Fu) solution of different concentrations were added to the experimental group. Add 10 μL of PBS and continue the culture; after 48 h, add 10 μL of MTT to each well, continue to culture in the incubator, stop the culture after 4 h, suck off the culture supernatant in t...
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