Application of Myriberine A in preparation of medicines for treating or preventing yellow fever virus infection
A yellow fever virus and drug technology, applied in antiviral agents, pharmaceutical formulations, resistance to vector-borne diseases, etc., to achieve the effect of strong inhibitory activity and prominent substantive characteristics
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Embodiment 1
[0012] Embodiment 1: the preparation of compound Myriberine A tablet involved in the present invention:
[0013] Get 20 grams of compound Myriberine A and add 180 grams of conventional excipients for preparing tablets, mix well, and make 1000 tablets with a conventional tablet press.
Embodiment 2
[0014] Embodiment 2: the preparation of the compound Myriberine A capsule involved in the present invention:
[0015] Get 20 grams of compound Myriberine A and add conventional adjuvants such as starch 180 grams for the preparation of capsules, mix well, and make 1000 capsules.
[0016] The following pharmacodynamic experiments will further illustrate its drug activity.
experiment example 1
[0018] A. Toxicity test of Myriberine A on Vero cells
[0019] Vero cells (African green monkey kidney cells) are susceptible cells to YFV.
[0020] The experimental steps are as follows:
[0021] 1: Inoculate Vero cells: Use DMEM medium containing 10% (v / v) fetal bovine serum to make a single cell suspension, inoculate 1000-10000 cells per well into a 96-well cell culture plate, and inoculate a volume of 100ul per well ;
[0022] 2: Cultivate Vero cells: at 37°C, 5% (v / v) CO2 culture conditions, culture for 2 days;
[0023] 3: Add Myriberine A: Discard the DMEM medium in each well, add 100ul to each well and dilute to the corresponding concentration with DMEM medium containing 10% (v / v) fetal bovine serum (0uM, 0.4uM, 1.2 uM, 3.7uM, 11uM, 33uM, 100uM, 300uM) Myriberine A, add 100ul of DMEM medium containing 10% (v / v) fetal bovine serum to the control well;
[0024] 4: Coloring: After 48 hours of culture, add 10ul of MTT solution to each well, continue to incubate for 4 ho...
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