Application of ramosissimonea in preparation of medicine for treating rheumatoid arthritis
A rheumatoid and arthritis technology, applied in the application field of Ramosissimone A in the preparation of drugs for the treatment of rheumatoid arthritis, which can solve the problems of induced infection, poor action selectivity, damage, etc.
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Embodiment 1
[0026] Inhibitory effect of Ramosissimone A on proliferation of rheumatoid arthritis.
[0027] Cell: Human rheumatoid synovial cells (RA-FLS);
[0028] Drug: Ramosissimone A;
[0029] Method: 1. RA-FLS recovery
[0030] The RA-FLS freezing pipe is quickly removed from the liquid nitrogen irrigation, and the temperature of the temperature of 37 ° C is placed, and the cells are uninterrupted, and the cells are thawed. After being refined, the RA-FLS suspension in the frozen tube was moved to 10 ml of sterile centrifugal tube in the ultimate platform, centrifuged for 5 min, and the rotational speed was 1000R / min. Inverted the supernatant, add 5 ml of fully cultured liquid, continuously blowing to a homogeneous cell suspension with pipette, inoculation of RA-FLS in a 25 ml cell culture flask, placed in a cell incubator, and incubator conditions are set to Temperature 37 ° C, CO 2 The concentration is 5%. After 24 hours, the growth of RA-FLS was observed under the microscope, and whe...
Embodiment 2
[0039] Promoting effect of Ramosissimone A on apoptosis of rheumatoid arthritis.
[0040] Cell: Human rheumatoid synovial cells (RA-FLS);
[0041] Drug: Ramosissimone A;
[0042] Method: 1. RA-FLS recovery
[0043] Similarly to Example 1.
[0044] 2.RA-FLS pass
[0045] Similarly to Example 1.
[0046] 3.Tuneel method to determine apoptosis
[0047] The breakage of chromosome DNA in apoptosis is a progressive stage of step, and the chromosome DNA first degrades a large fragment of 50-300 kB in the endogenous nucleic acid hydrolase. Then approximately 30% chromosome DNA in CA 2+ And MG 2+ Under the dependent nucleic acid endozyme, the nucleic body unit is randomly cut, and 180 to 200 bp nucleom DNA polymer is formed. DNA Double-strand break or a series of DNAs generated by a gap in a chain can cause deoxyribonucleotides and fluorescene under the action of deoxyribonucleotide terminal transferase (TDT). The derivatives formed by peroxidase, alkaline phosphatase or biotin is labeled to...
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