Application of Tripterygium wilfordii alkaloid extract in preparation of drugs used for preventing or treating avian influenza
A tripterygium wilfordii alkaloid and extract technology, which can be used in drug combinations, pharmaceutical formulations, plant raw materials, etc., can solve the problems of strong irritation and corrosiveness of the environment and animals, unsuitable disinfection, and high disinfection costs.
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Embodiment 1
[0010] Embodiment 1: the research of Tripterygium wilfordii on the effect of avian influenza virus
[0011] Chicken Embryo Test and Determination of Therapeutic Index
[0012] 1. Experimental materials
[0013] Test drug: Tripterygium wilfordii alkaloid extract of the present invention;
[0014] Positive control substance: amantadine (purchased from Shijiazhuang Shengdian Pharmaceutical Co., Ltd.);
[0015] Blank control: distilled water;
[0016] Virus source: chicken-derived H5 subtype avian influenza virus [AIV (H5N1)] (from the virus room of the Animal Institute of South China Agricultural University);
[0017] Experimental chicken embryos were purchased from the Experimental Poultry Farm of South China Agricultural University.
[0018] 2. Experimental method
[0019] 1) Determination of the half-inhibitory dose (IC) of the test drug 50 )
[0020] 2) Determine the half toxic dose of the drug
[0021] 3) Viral potency of test drugs
[0022] The half effective dose ...
Embodiment 2
[0028] Embodiment 2: the test of the viral pneumonia that treatment H5N1 type avian influenza virus causes
[0029] 1. Materials
[0030] Test drug: Tripterygium wilfordii alkaloid extract of the present invention;
[0031] Positive control substance: amantadine (purchased from Shijiazhuang Shengdian Pharmaceutical Co., Ltd.);
[0032] Blank control: normal saline;
[0033] Experimental animals: Kunming mice (6 weeks old, mixed male and female) provided by the Experimental Animal Laboratory of Southern Medical University were injected with H5N1 virus to prepare a mouse viral pneumonia model.
[0034] 2. Experimental method:
[0035] 30 mice were randomly divided into 3 groups. They were low (0.36mg / ml), medium (0.49mg / ml), high dose (0.72mg / ml), amantadine (0.5mg / ml) and blank control groups respectively. The blank control group was intraperitoneally injected with normal saline at 15ml / kg; the amantadine group was injected intraperitoneally at 15ml / kg for 7 consecutive da...
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