Pharmaceutical use of sophoricoside
A technology of sophorin and medicine, which is applied in the field of pharmaceutical application of sophorin, and can solve the problems of increasing the incidence of breast cancer and endometrial cancer
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Embodiment 1
[0047] Embodiment 1: Animal grouping and modeling
[0048] Sixty-six 6-month-old female SD rats were randomly divided into model group (ovariectomized, OVX), sham operation group (SHAM), and various drug intervention groups: ERT group, selective estrogen receptor modulator (SERM) group, cents Linggubao group, Sophoroside 10 mg group (HDA10), Sophoroside 20 mg group (HDA20), Sophoroside 40 mg group (HDA40), Sophoroside 80 mg group (HDA80).
[0049] 1. Modeling method:
[0050]OVX group and each drug intervention group: 1% pentobarbital sodium solution, 5ml / kg, intraperitoneally injected, after the anesthesia took effect, the rats were placed in a prone position, the hair was removed at the third lumbar vertebra under the costal arch, and benzalkonium bromide was administered. Disinfect the skin with ammonium tincture, cut the skin, incision about 1cm long, cut the subcutaneous and fascia, bluntly separate the muscles, carefully incise the peritoneum, extend the tissue forceps ...
Embodiment 2
[0066] Embodiment 2: Rat body weight and uterine wet weight before and after the experiment
[0067] The body weight of the rats was weighed before and after the experiment, and the wet weight was taken from the uterus at the same time when the samples were sacrificed. The results are shown in Table 1.
[0068] Table 1 Rat body weight and uterine wet weight before and after the experiment (x±S x )
[0069]
[0070] Note: Compared with the SHAM group: ** P* P<0.05; compared with OVX group: △△P<0.01, △P<0.05.
[0071] Statistical analysis of variance was used to analyze the data. There was a large difference in uterine wetness in the SHAM group, which was considered to be caused by different menstrual cycles. There was no statistical difference in body weight among the groups before and after the experiment. There was a statistically significant difference in uterine wet weight between the ovariectomized groups and the SHAM group (P0.05), suggesting that estrogen has a st...
Embodiment 3
[0072] Embodiment 3: Observation of uterine slices:
[0073] 1. Embedding: Fix the rat uterus obtained in Example 1 with 4% paraformaldehyde for 24 hours; 75% alcohol dehydration overnight; 85% alcohol dehydration for 45 minutes; 95% alcohol dehydration for 45 minutes × 2; 100% alcohol dehydration for 45 minutes minutes × 2; immerse in xylene for 15 minutes × 2; oven at 65°C, soak in wax for 3 hours; embedding in paraffin.
[0074] 2. Slicing: take the coronal surface of rat uterine lumen, slice it with a paraffin microtome (Leica, Model: RM2235), 5 μm in thickness, put it in warm water at 30° C., and treat the slide with polylysine. Bake the slices in a 65°C oven for 3 hours and slice them for later use.
[0075] 3. HE staining of the uterus: 1) Dewax the slices to water: 65°C oven for 3 hours; immerse in xylene for 10 minutes × 3; 100% alcohol for 10 minutes × 2; 95% alcohol for 10 minutes × 2; 85% alcohol for 10 minutes; 75% alcohol for 10 minutes; double distilled water....
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