Application of fluevirosines A in the preparation of drugs for inhibiting liver fibroblast proliferation
A technology of fibroblasts and drugs, which can be used in drug combinations, pharmaceutical formulations, organic active ingredients, etc., and can solve problems such as lack of clinical treatment methods
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Embodiment 1
[0010] Embodiment 1: the preparation of the compound Fluevirosines A tablet involved in the present invention:
[0011] Take 5 grams of compound Fluevirosines A, add 195 grams of dextrin, mix well, and make 1000 tablets by conventional compression.
Embodiment 2
[0012] Embodiment 2: the preparation of compound Fluevirosines A capsules involved in the present invention:
[0013] Get 5 grams of compound Fluevirosines A, add 195 grams of starch, mix well, and pack into capsules to make 1000 capsules.
[0014] The following pharmacodynamic experiments will further illustrate its drug activity.
experiment example 1
[0015] Experimental example 1: MTT method was used to evaluate the inhibitory effect of the compound Fluevirosines A on liver fibrosis
[0016] 1. Method: NIH / 3T3 cell line was purchased from the cell bank of Shanghai Institute of Cellular Sciences, Chinese Academy of Sciences, cited from ATCC (American Type Culture Collection). Subconfluent NIH / 3T3 cells in the logarithmic growth phase were digested with 0.25% trypsin, washed, centrifuged, and made 1×10 with DMEM medium (containing 10% FCS). 4 cell / ml cell suspension, the survival rate identified by trypan blue staining is greater than 95%, add 100ul per well to a 96-well plate, and store at 37°C, 5% CO 2 After 24 hours of culture and synchronous treatment, the supernatant was discarded, and 200ul of DMEM culture solution (containing 10% FCS) containing different dilutions of drugs was added, cultured for 48 hours, and MTT solution was added to each well for incubation for 4 hours. Discard the culture medium, add 150ulDMSO, ...
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