Medicine combination and application thereof in preparing preparations for treating chronic hepatitis B
A technology for chronic hepatitis B and its composition, which is applied in the field of preparation of preparations for treating chronic hepatitis B, can solve the problems of repeated disease, drug resistance, HBV mutation, etc., and achieve the effect of regulating immune function and enhancing immunity
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Embodiment 1
[0019] The BCG polysaccharide nucleic acid required by the present invention can be obtained by the following methods, but those skilled in the art can understand that the preparation of BCG polysaccharide nucleic acid includes but is not limited to this method:
[0020] 1) Cultivation and harvest of BCG
[0021] 1. Bacterial cell culture: dissolve the liquid cryopreserved strain (BCG strain D2PB302 for the preparation of BCG vaccine in China, China Institute for the Control of Pharmaceutical and Biological Products) at room temperature, inoculate it in potato Sutong medium, and continuously cultivate at 37°C for 14-20 days ; Or cultivated continuously at 37℃ for 15 days and then transferred to modified liquid Sutong medium, and cultivated continuously at 37℃ for 14-20 days.
[0022] 2. Bacteria collection: When the bacteria grow to the logarithmic phase, check the culture flask bottle by bottle, collect the bacterial membrane, add an appropriate amount of deionized distilled water t...
Embodiment 2
[0039] The method for producing powder injection of pharmaceutical composition with BCG polysaccharide nucleic acid as the active ingredient, the prescription is:
[0040] BCG nucleic acid: 0.3g
[0041] Physiological sodium chloride solution (0.9%): 100ml
[0042] Take a prescription amount of ordinary lyophilized powder D BCG polysaccharide nucleic acid and an appropriate amount of water for injection and mix evenly. Those skilled in the art can also understand that the BCG polysaccharide nucleic acid can be in the form of micropowder, solid dispersion, inclusion compound, microsphere, Add in the form of liposomes or microparticles. After fully dissolving, centrifuge at 4000 rpm and 3°C for 15 minutes. Take the supernatant and test the content of polysaccharide and nucleic acid. After the test is qualified, the supernatant passes 0.22 The μm filter is finely filtered, and the filtrate is autoclaved and steam-sterilized and then packed into vials, freeze-dried, stoppered, and cappe...
Embodiment 3
[0044] The preparation method of the pharmaceutical composition injection with BCG polysaccharide nucleic acid as the active ingredient, the prescription is:
[0045] BCG nucleic acid: 0.3g
[0046] Physiological sodium chloride solution (0.9%) or water for injection: 100ml
[0047] Take the prescription amount of BCG polysaccharide nucleic acid and appropriate amount of physiological sodium chloride solution (0.9%) or water for injection, mix well, dissolve it thoroughly, centrifuge at 4000 rpm, 3°C for 15 minutes, take the supernatant, and proceed The content of polysaccharide and nucleic acid is tested. After the test is qualified, the supernatant is filtered through a 0.22μm filter, and then filled in an ampoule, and autoclaved steam sterilization can be injected into a pharmaceutical composition with BCG polysaccharide nucleic acid as the active ingredient liquid. Give the patient an intramuscular injection of 1 ml every other day.
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