Composition for preventing enveloped virus infection and its preparation method and application
A technology of virus infection and composition, which is applied in the field of composition for preventing enveloped virus infection and its preparation, can solve the problems of easy mutation of virus and difficulties in clinical disease prevention and treatment, achieve strong inhibitory and killing effects, wide range of antiviral effects, Guarantee the effect of normal production
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Embodiment 1~5
[0093] The specific data of component composition weight ratio among the embodiment 1~5 is as shown in Table 1:
[0094] Table 1 Component composition table in Embodiments 1 to 5
[0095]
[0096]
[0097] Specific preparation process:
[0098] (1) According to the weight ratio of the formula, weigh A component, B component, C component, and D component respectively, and make each component mix uniformly, and set aside;
[0099] (2) Add disodium ethylenediamine tetraacetate to the uniformly mixed component D in an amount of 5-25g / kg, stir and mix uniformly, and prepare premixture E;
[0100] (3) Add a surfactant in the prepared premix E, the addition amount is 5-25g / kg, after stirring and mixing uniformly, the premix F is prepared;
[0101] (4) Add vitamin E and vitamin C to the prepared premixture F, the amount of vitamin E added is 5-50 g / kg, the amount of vitamin C added is 5-50 g / kg, after stirring and mixing uniformly, the premix G is prepared;
[0102] (5) In tu...
Embodiment 6
[0105] The toxicological test of the composition for preventing enveloped virus infection is as follows:
[0106] Acute toxicity test:
[0107] Experimental observation, because the LD50 cannot be measured, so the determination of the maximum dosage was carried out. The compositions for the prevention of enveloped virus infection prepared in Examples 1-5 were formulated into oral liquids using physiological saline or glucose, and were directly administered to mice. The results showed that the maximum drug administration concentration was 11.84 crude drug / ml, and the maximum administration volume 50ml / kg was intragastrically administered to mice twice within 24 hours, and the maximum dose of the drug administered to mice was 400g crude drug / kg. No adverse reaction or death occurred in the animals, and no abnormalities were found in the organs under anatomical observation.
[0108] Long-term toxicity test:
[0109] In this experiment, 200 SD rats were used, and the composition...
Embodiment 7
[0111] In this example, in order to verify the preventive effect of the composition for preventing enveloped virus infection of the present invention on poultry viral diseases, based on the components provided in Examples 1-5, the following experiments were carried out:
[0112] 1. Prevention of Newcastle disease infection
[0113] 1. Selection of experimental animals: 300 chicks at the age of 25 days.
[0114] 2. Experimental drugs and equipment:
[0115] Newcastle disease virus, scales, scientific calculator.
[0116] 3. Experimental grouping and processing:
[0117] Randomly divided into 6 groups, 50 pigeons in each group, the classification and treatment of each group are as follows:
[0118] Five test groups:
[0119] Prepare the composition for preventing enveloped virus infection provided by Examples 1-5, add it to the diet, feed it to chickens, and drink water freely for 15 days;
[0120] A control group:
[0121] The chickens were fed with normal rations and had...
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Abstract
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