Oral liquid for treating osteoporosis
A technology of oral liquid for osteoporosis, applied in the field of oral liquid for the treatment of osteoporosis, which can solve the problems of uncertain long-term curative effect, large toxic and side effects, and high price
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Embodiment 1
[0012] Example 1 Research on the Action Mechanism of Drugs of the Present Invention on Ovariectomized Rats
[0013] 1. Selection and grouping of animals
[0014] 26 female SD rats aged 6 months were selected to undergo bilateral ovariectomy under chloral hydrate anesthesia, and 8 rats were in the sham operation group. The ovariectomized rats were divided into 8 pathological control groups, 9 estradiol groups and 9 drug treatment groups of the present invention.
[0015] 2. Prescription preparation
[0016] According to the ratio of Epimedium 12-15, Rehmannia glutinosa 15-20, Astragalus 15-20, Eucommia 15-20, Psoralen 20-30, Drynaria 20-30, soak and decoct in 20 times distilled water, and the filtrate is centrifugally concentrated Precipitate with 75% ethanol, recover ethanol; adjust pH to 7.0; add activated carbon for decolorization; make a medicinal solution containing crude drug 2g / ml. (note, following embodiment 2,3,4 also adopts same method to configure medicine of the ...
Embodiment 2
[0037] Example 2 Effects of Drugs of the Present Invention on Proliferation and Differentiation of Rat Bone Marrow Stromal Stem Cells
[0038] (1) Reagents: fetal bovine serum (product of Hangzhou Sijiqing Company), DMEM medium (product of Gibco Company in the United States), trypsin and tetramethylazozolium salt (MTT reagent is product of Sigma Company), alkaline phosphatase (product of Sigma Company), ALP) kit.
[0039] (2) Instrument: Inverted Microscope (Nikon Company), CO 2 Incubator, cell culture plate (product of Gibco, USA), 723 spectrophotometer, ELX808 microplate reader (product of BioTek, USA).
[0040] (3) Isolation and culture of MSCs: Femurs of rats were taken, and both ends were removed to flush out the bone marrow. Add 10% medium, set at 37°C, 5% CO 2 , with about (2~5)×10 4 / cm 2 Density seeded in culture flasks, placed in 5% CO 2 Cultivate in an incubator, and subculture after the cells are congested.
[0041] (4) the influence of the medicine of the p...
Embodiment 3
[0056] Example 3 The Drug of the Present Invention Antagonizes Dexamethasone to Promote the Differentiation of Bone Marrow Stromal Cells into Adipogenic Cells
[0057] (1) Isolation and culture of MSCs
[0058] After the cells were congested, they were subcultured, and the third-generation cells were used for experiments, and divided into dexamethasone (1×10 -7 mol / L) group, dexamethasone plus medicine of the present invention (80mg / L) group and matched group (conventional serum culture). Cell growth was observed under an inverted microscope.
[0059] (2) Effect of medicine of the present invention and dexamethasone on MSCs proliferation
[0060] Table 1 The influence (x ± s) of medicine of the present invention and dexamethasone on MSCs proliferation
[0061]
[0062] *p<0.05 compared with the control group, A: dexamethasone group, B: dexamethasone plus the drug group of the present invention, C: control group.
[0063] Results: MTT assay showed that dexamethasone coul...
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