Compound with immunity-enhancing effect and application thereof in preparation of medicine for improving immunity
A compound and immunity technology, applied in the field of preparation of immunity-enhancing drugs, can solve the problems of poor water solubility, unstable chemical sites, and far-reaching efficacy of andrographolide, and achieve the purpose of improving immunity. Active application, extraction The separation method is simple and has no toxic and side effects
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Embodiment 1
[0032] S1. According to the method under the Fuke Qianjin Capsule in the Pharmacopoeia of the People's Republic of China [1] Extract from Zhuzhou Qianjin Pharmaceutical Co., Ltd. and prepare 1.5kg of Fuke Qianjin Prescription Extract Dry Cream (FKQJ). This dry paste was extracted 8 times with 3 times the volume of EtOAc to obtain an EtOAc extract (FKQJE, 156g);
[0033] S2. Take the EtOAc extract (FKQJE, 142.2g) and mix the sample with silica gel, then go through silica gel (1kg, 200-300 mesh) column chromatography, cyclohexane-EtOAc (9:1, 8:2, 7:3, 6:4 , 5:5, v / v) gradient elution, TLC detection and merging of similar fractions, a total of 10 fractions were obtained, respectively named: Fr.1, Fr.2, Fr.3, Fr.4, Fr. 5. Fr.6, Fr.7, Fr.8, Fr.9, Fr.10, spare;
[0034] S3. the fraction Fr.5 (11g) collected in step S2 is removed pigment (MeOH:H by MCI column chromatography) 2 O=5:5, 6:4, 7:3, 8:2, 9:1, v / v), TLC detection and merging of similar fractions, a total of 3 sub-fractio...
Embodiment 2
[0043] Embodiment 2 The effect of the compound of the present invention on mouse spleen lymphocyte proliferation
[0044] 1. Experimental method
[0045] (1) Spleen lymphocyte culture
[0046] Balb / c pure line mice, male or female, 8 weeks old. The mice were killed by cervical dislocation, the spleens of the mice were aseptically removed, cut into pieces and ground in RPMI1640 complete medium, and filtered through a 180-mesh sieve to obtain a single-cell suspension, and the number of cells was adjusted to 1×10 6 / mL. Add the cell suspension into a sterilized 96-well cell culture plate, 100 μl per well;
[0047] (2) Experimental grouping
[0048] The experiment was divided into blank group, lipopolysaccharide group and concanavalin A group, all of which were added with RPMI1640 complete medium containing different components, with a volume of 100 μl.
[0049] Blank group: add 100 μl RPMI1640 complete medium;
[0050] Lipopolysaccharide (LPS) group: add LPS to a final conc...
Embodiment 3
[0061] Embodiment 3 The effect of the compounds of the present invention on the phagocytosis of macrophages
[0062] 1. Experimental method
[0063] (1) Experimental grouping
[0064] 70 Balb / c pure-line mice, weighing 18-22 g, half male and half male, were randomly divided into 7 groups, 10 mice per group. The experiment set up a blank control group, a cyclophosphamide group (CY group), and 5 drug administration groups.
[0065] The blank control group was not injected;
[0066] CY group: inject cyclophosphamide 50mg / kg twice;
[0067] 5 administration groups: intragastric administration of drugs Fr.5-110mg / kg, 50mg / kg, 100mg / kg, 200mg / kg, 500mg / kg every day.
[0068] (2) Experimental treatment
[0069] The blank control group and CY group were intragastrically administered distilled water for 2 consecutive weeks (14 days), once a day; the treatment group was intragastrically administered for 2 consecutive weeks (14 days), once a day; The drug group was intraperitoneall...
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