Application of qi-tonifying and pulse-restoring (freeze-drying) or ruscogenin for injection in prevention of pharmaceutical organ hemorrhage
A technology of ruscogenin, nourishing qi and Fumai, which can be applied in the directions of drug delivery, drug combination, and drug formulation, etc., can solve the problems of increasing endothelial cell permeability, vascular leakage, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Improvement effect of Yiqi Fumai for injection (lyophilized) and its active ingredient (ruscogenin) on dasatinib-induced gastrointestinal bleeding in mice.
[0039] experimental method:
[0040] a) Experimental animals
[0041] The experimental animals are C57BL / 6J mice, weighing 18-22g, SPF grade, purchased from the Comparative Medicine Center of Yangzhou University, which meet the quality standards of ordinary experimental animals. License number: SCXK (Su) 2012-0001. The mice were reared in separate cages, free to drink and eat, the room temperature was 23-25°C, the relative humidity was 40%-80%, and the experiment was started after about one week of adaptive feeding.
[0042] b) Preparation of experimental drugs
[0043] Weigh 33.6mg of YQFM, add 1mL of normal saline solution, fully dissolve, this is the drug concentration of the low dose group; weigh 67.1mg of YQFM, add 1mL of normal saline solution, fully dissolve, this is the drug concentration of the middle d...
Embodiment 2
[0050] Yiqi Fumai injection (freeze-dried) and its active ingredient ruscogenin in improving the barrier damage of human umbilical vein endothelial cells induced by dasatinib.
[0051] experimental method:
[0052] a) Cell culture: HUVECs were cultured with 10% FBS RPMI 1640 medium after recovery. When the cells are about 90% confluent, discard the medium and rinse with PBS. Add 0.25% trypsin solution, digest in a 37°C incubator, observe the roundness of the cells under a microscope, discard the digestion solution and add RPMI 1640 culture solution containing 10% FBS to terminate the digestion. Blow down the cells and transfer to a centrifuge tube, and collect the cells by centrifugation. Discard the supernatant, add RPMI 1640 culture medium containing 10% FBS and blow it into a cell suspension, pass on a new cell culture dish, and culture at 37°C in a 5% CO2 incubator.
[0053] b) Measurement of transendothelial cell resistance: 200 μl (3-5x10 4 pcs / well) into the Millice...
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