Traditional Chinese medicine composition for treating myelodysplastic syndrome and applications thereof
A technology for myelodysplasia and syndrome, applied in drug combinations, pharmaceutical formulas, plant raw materials, etc., can solve problems such as expensive treatment costs, high risks related to transplantation, and chemotherapy insensitivity, and achieve the effect of broadening the range of drug selection
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Embodiment 1
[0030] 1Kg dry coarse powder of C. chinensis, heated and refluxed with 12000mL of 80% ethanol for 3 times, 2h each time, combined the extracts, concentrated under reduced pressure to obtain 100g thick extract. Add 500mL of water to form a suspension, and extract three times with 500mL of petroleum ether, 500mL of chloroform, and 500mL of n-butanol. Take the n-butanol extract, recover it to dryness under reduced pressure, and obtain the n-butanol fraction (40g), mix the sample with thick silica gel (800g), load the sample on a silica gel (100-200 mesh) column, and wash with chloroform-methanol (80 :20) elution, the resulting fraction is recovered to dryness under reduced pressure to obtain component a11g.
[0031] Eucommia ulmoides leaves 1kg dry coarse powder, heated and refluxed with 10000mL of 80% ethanol for 3 times, 2h each time, combined extracts, concentrated under reduced pressure to obtain 130g of thick extract. Add 500mL water to form a suspension, and extract three ...
Embodiment 2
[0034] Embodiment 2: The application of Chinese medicine composition effective component (PHDE) to myelodysplastic syndrome inhibition
[0035] (1) Cell culture
[0036] The human MDS cell line Skm-1 cell line was donated by the Institute of Blood Diseases of the First Affiliated Hospital of Zhejiang University School of Medicine. The cell line was established from a high-risk MDS patient by Japanese scholar Nakagawa. The cell culture conditions were 10% GIBCO Fetal Bovine Serum RPMI1640 complete medium at 37°C, 5% CO 2 cultured in an incubator and subcultured once a day.
[0037] (2) MTT method to detect cell viability
[0038] Take Skm-1 cells in the logarithmic growth phase and suspend them in RPMI1640 medium. After counting, count them according to 5×10 4 cells / mL were implanted into 24-well culture plates, 1 mL per well. In the experiment, a drug-dosing group and a control group were set up: the drug-dosing groups had drug concentrations of 0.05, 0.075, 0.1, and 0.125...
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