Pseudolaric acid B and application of derivative thereof in preparation of immunity inhibitor
An immunosuppressant, hibiscus acetic acid technology, applied in anti-inflammatory agents, drug combinations, non-central analgesics, etc., can solve the inability to completely prevent the immune response of transplanted tissues, side effects, and inability to completely suppress rejection with tolerated doses, etc. problem, achieve excellent immunosuppressive effect and low toxicity
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Embodiment 1
[0034] Example 1: Proliferation of T and B Lymphocytes Stimulated by Mitogens
[0035] Aseptically take the mouse spleen, grind it to prepare a single cell suspension, remove red blood cells, and adjust the cell concentration to 5×10 with RPMI-1640 culture medium containing 10% fetal bovine serum (FBS). 6 / mL. Add 100 μl / well of cell suspension in a 96-well plate, and 50 μl / well of different concentrations of samples (hibiscus acetic acid, hexahydro hibiscus acetic acid, deacetylated (R 3 )- hibiscus acetic acid, demethylation (R 2 )- hibiscus acetic acid or deacetylated (R 3 ) Demethylation (R 2 )- Hibiscus acetic acid, BP-1, BP-3, BP-15, BP-20, BP-2, BP-5, BP-6, BP-7, BP-8, BP-10, BP-11, BP-12, BP-13, BP-14, BP-16, BP-17 (BP-18, BP-19) solution, concanavalin A (ConA) or lipopolysaccharide (LPS) of 50 μl / hole, control plus etc. volume medium. After mixing, store at 37°C, 5% CO2 conditions for 48 hours. 4 to 6 hours before the end of the culture, 100 μl of 5 mg / mL MTT s...
Embodiment 2
[0039] Example 2: Unidirectional mixed lymphocyte culture
[0040] Spleen of BALA / c mice was aseptically taken to make a single cell suspension, and the spleen cells of BALA / c mice as stimulatory cells were diluted to 1×10 with complete RPMI-1640 medium. 7 / mL, inactivated with 50 μg / mL mitomycin C in a 37°C water bath, shaken once every 15 minutes, washed three times with PBS, and diluted to 5×10 with complete RPMI-1640 medium 6 / mL. C57BL / 6 mouse splenocytes were used as responding cells. Take 100 μl / well of the above mixture of stimulating cells and responding cells, add different concentrations of hibiscus acetic acid 100 μl / well, add the same amount of medium for the negative control, and add 8×10 -9 M Cyclosporin A (CsA). 37°C, 5% CO 2 Conditioned for 3 days. Added 12h before the end of culture 3 H dilution 25 μl, cells were harvested at the end of incubation, radioactive incorporation was measured by liquid scintillation counting, and data were expressed as pulses...
Embodiment 3
[0051] Example 3: Induction and detection of cytokine production
[0052] Take the spleen of the mouse aseptically, grind it to prepare a single cell suspension, remove the red blood cells, and adjust the cell concentration to 5×10 with RPMI-1640 culture medium containing 10% FBS 6 / mL, cultured in a 96-well plate, 200 μL per well, 3 replicate wells in each group, anti-CD3 monoclonal antibody (anti-CD3) 0.2 μg / mL) was added to the cell suspension, and the drug intervention group was anti-CD3+ different Concentration of Hibiscus acetate arginine salt, negative control plus equal volume medium, positive control plus 8×10 -9 M Cyclosporin A (CsA). 37°C, 5% CO 2 The supernatant was collected after 72 hours of culture under conditions, and the production of IFN-γ was detected by double-antibody sandwich enzyme-linked immunosorbent assay (ELISA). The absorbance was measured at OD450nm with a microplate reader, and the content of cytokines in the samples was converted according to...
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