Duck viral hepatitis resisting astraglus polysaccharide phosphorylated molecular modification method
A technology of duck viral hepatitis and astragalus polysaccharides, which is applied in the direction of antiviral agents, organic active ingredients, and medical preparations containing active ingredients, can solve problems such as loss, and achieve the effect of convenient use and good water solubility of the preparation
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2016-05-11
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Abstract
Description
1. Technical field
[0001] The invention relates to a method for modifying phosphorylated molecules of astragalus polysaccharides against duck viral hepatitis, and belongs to the technical field of preparation of traditional Chinese veterinary medicines. 2. Background technology
[0002] Duck viral hepatitis is a disease caused by duck hepatitis virus (DHV) infection that spreads rapidly, has a high morbidity rate, and is highly fatal. The virus was first isolated in 1949 and is now distributed worldwide. DHV mainly has three serotypes: DHV-1 and its variants, DuckAstrovirus and DHV-3, among which DHV-1 is the most toxic and widely distributed, mainly infecting ducklings under 3 weeks old, with a fatality rate higher than 80% %, even up to 100%, is one of the main pathogens that seriously endanger the duck industry.
[0003] At present, there is no effective anti-DHV-1 drug clinically in the world, and the immune defense is mainly carried out by injecting attenuated vaccine...
Examples
Embodiment Construction
[0016] 1. Extraction of astragalus polysaccharide and screening of effective parts
[0017] Weigh 1000g of astragalus, add 10 times the amount of water to soak for 3 hours, heat and boil for 1 hour, collect the decoction, and repeat 3 times; combine the collected decoction, boil and concentrate to 1000mL, centrifuge with a high-speed centrifuge, and take the supernatant. Slowly add ethanol with different volume fractions of 95% to the concentrated solution so that the ethanol content in the solution is 50%, 65%, 75% and 80% respectively, let it stand overnight, and collect the precipitates by centrifugation respectively. After dialysis with running water, vacuum concentration, 3000rpm / min, centrifugation for 20min, the supernatant was again added with different volume fractions of 95% ethanol for precipitation, repeated dialysis, concentration, and centrifugation, repeated 3 times, vacuum dried at 60°C, and crushed to obtain Astragalus membranaceus APS of different alcohol pre...