Application of Incarvillea delavay alkali in preparing drug for resisting autoimmune diseases and graft rejection diseases
An autoimmune disease, pineapple alkaloid technology, applied in metabolic diseases, skin diseases, bone diseases and other directions, can solve the problems of cell non-specificity, increase the economic burden of patients, and high prices, achieve inhibition of occurrence and development, save treatment costs, Source-rich effects
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Embodiment 1
[0036] Example 1: 30 kg of the whole herb of Incarvillea delavay was extracted 3 times with 200 L of 80% ethanol under reflux, each time for 2 hours, the extracts were combined, concentrated under reduced pressure to obtain 600 g of extract, diluted with water and then diluted with 2% HCl , adjust the pH to 2-3, filter to obtain the filtrate and filter residue, add 20% NaOH to the filtrate to adjust the pH to 11, extract with chloroform to obtain the chloroform fraction; concentrate the extraction fraction under reduced pressure to obtain 250 g of crude product. Mix the crude product with 500g of silica gel, add it to the top of the installed silica gel column, and elute with the gradient of chloroform-acetone (20:1~2:1) system, collect the fraction containing bromelain, and then react with C18 Phase column chromatography, eluting with methanol-water (50%-70%), and thin-layer chromatography detection, obtained 2320 mg of pure bromelain.
Embodiment 2
[0037] Example 2 In vitro culture of human dendritic cells and treatment of DCs with bromelain
[0038] Take 50ml / person of peripheral blood from healthy adults intravenously, anticoagulate with heparin, separate peripheral blood mononuclear cells by density gradient centrifugation, suspend cells in RPMI1640 (1640 medium) containing 10% calf serum, and adjust the cell concentration to 2× 10 6 / ml, add to 24-well culture plate, 0.5ml / well, incubate at 37°C, 5% CO2 for 2 hours, make the mononuclear cells adhere to the wall, wash the culture plate lightly with warm serum-free RPMI1640 to remove the adherence cells, that is, to obtain adherent monocytes. Add serum-containing RPMI1640 containing rhGM-SCF (human recombinant granulocyte colony-stimulating factor) 1000IU / ml and rhIL-4 (human recombinant interleukin 4) 800IU / ml to the culture plate, and incubate at 37°C with 5% CO2 Cultivate in box for 5 days, add bromelain with a final concentration of 2 μmol / L for 24 hours, and the...
Embodiment 3
[0040] Example 3 Effect of bromelain on secretion of IL-10 by human dendritic cells
[0041]According to the method of Example 1, the dendritic cells of the bromelain-stimulated group and the unstimulated group were cultured, the supernatant was collected, and the IL-10 content was detected with an IL-10 ELISA (enzyme-linked immunosorbent assay) kit. The concentration of IL-10 secreted by mononuclear cells transformed dendritic cells in vitro in the pineapple flower stimulation group and the unstimulated group was 435 ± 22pg / ml, 92 ± 14pg / ml, and there was a significant difference (Pfigure 1 ).
[0042] Example 3 Separation of T cells and the effect of bromelain on T cell transformation
[0043] 50ml / person of healthy adult peripheral blood was extracted intravenously, anticoagulated with heparin, and peripheral blood mononuclear cells were isolated by density gradient centrifugation, cultured in RPMI1640 serum-free medium for 2 hours, suspended cells were collected, and after...
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