Application of java brucea fruit fat-soluble extract in preparation of drugs for promoting peripheral nerve regeneration
A fat-soluble extract, peripheral nerve technology, applied in the field of biomedicine, can solve problems that have not yet been discovered
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] The preparation of embodiment 1 lipid-soluble extract of Brucea javanica
[0027] Bructus javanica was purchased from Nantong Hospital of Traditional Chinese Medicine, washed with deionized water, dried in an oven at 60-65°C for 2 days, and then ground into powder (300g). Accurately weigh 50 g of Brucea javanica dry powder, put it into an extraction vessel, and soak it in mixed solutions of absolute ethanol and ethyl acetate of different concentrations for 48 hours at room temperature (22°C). Grouping: 95% absolute ethanol + 5% ethyl acetate; 85% absolute ethanol + 15% ethyl acetate; 75% absolute ethanol + 25% ethyl acetate; 65% absolute ethanol + 35% ethyl acetate; 55% absolute ethanol + 45% ethyl acetate; 45% absolute ethanol + 55% ethyl acetate; 35% absolute ethanol + 65% ethyl acetate; 25% absolute ethanol + 75% ethyl acetate; 15% Absolute ethanol + 85% ethyl acetate; 5% absolute ethanol + 95% ethyl acetate. The soaking solutions with different concentrations were...
Embodiment 2
[0028] The extraction effect of the dehydrated alcohol and ethyl acetate mixed solution of embodiment 2 different concentrations
[0029] In order to detect the effect of the fat-soluble mixture of Brucea javanica extracted with different concentrations of absolute ethanol and ethyl acetate on the growth of nerve cells, the experiment took the nerve cell line PC12 cells as the observation model.
[0030] PC12 cells were cultured in DMEM complete medium (containing 10% horse serum, 5% fetal bovine serum, 100 U / ml penicillin, 100 μg / ml streptomycin) in a petri dish, placed in 5% CO 2 , Cultivated in a 37°C incubator. The medium was changed every two days, and the cells were passaged when they grew to 80% confluence. In the experiment, PC12 cells in the logarithmic growth phase were taken, and 5×10 4 / ml Seed cells in 24-well culture plate, 400μl per well. After 24 hours, it was replaced with DMEM medium containing 1% horse serum and 1% fetal bovine serum. The experiments wer...
Embodiment 3
[0034] Example 3 Cytotoxicity Detection of Brucea Brucea Fat-Soluble Extract
[0035] The lipid-soluble extract of Brucea javanica prepared in Example 1 was lyophilized overnight (EYELAFDU-1200, Tokyo), and the obtained powder was put into a 15ml centrifuge tube and stored at 4°C. Prepare a 10μg / mL solution with sterile deionized water, centrifuge at 8000g for 10min, and then prepare the solution to the concentration required for the experiment, and then use a 0.2mm nylon syringe filter (Millipore, USA) to filter and sterilize the cultured PC12 Cytotoxicity tests were performed in cell lines. The CCK8 kit was purchased from Japan Dojin Chemical Research Institute.
[0036] Take PC12 cells in the logarithmic growth phase, digest, count and resuspend, and adjust the cell density to 5×10 5 / mL, inoculate 100 μL per well in a 96-well plate; after the cells adhere to the wall, discard the medium and wash with 0.01 MPBS for 5 min×2 times. The negative control group was 1% horse s...
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