Sustained-release pharmaceutical composition for treating allergic rhinitis as well as preparation method and application thereof
A technology for allergic rhinitis and sustained-release drugs, which is applied in the directions of drug combination, drug delivery, pharmaceutical formulation, etc., can solve the problems of reduced efficacy, side effects of oral preparations, and inability of sprays to be sprayed into edema, so as to reduce drug resistance. , the effect of improving the curative effect
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Embodiment 1
[0023] A sustained-release pharmaceutical composition for treating allergic rhinitis, comprising the following raw materials according to mass-volume concentration: loratadine 0.5 mg / ml, cromolyn disodium 16 mg / ml, dexamethasone 0.1 mg / ml, hydrochloric acid Ephedrine 8mg / ml, levofloxacin 4mg / ml, and the sustained-release pharmaceutical composition also includes citric acid.
[0024] The sustained-release pharmaceutical composition also includes a film matrix, and the film matrix includes film materials, plasticizers, surfactants, porogens and solvents.
[0025] The film material is polyvinyl alcohol, hypromellose, hypromellose.
[0026] The plasticizer is glycerin.
[0027] The surfactant is polysorbate-80.
[0028] The porogen is polyethylene glycol.
[0029] Described solvent is ethanol, water and acetone.
[0030] The preparation method of the sustained-release pharmaceutical composition for the treatment of allergic rhinitis, the steps are as follows:
[0031] 1) Weig...
Embodiment 2
[0035] A sustained-release pharmaceutical composition for treating allergic rhinitis, comprising the following raw materials according to mass-volume concentration: loratadine 0.8mg / ml, cromolyn disodium 20mg / ml, dexamethasone 0.18mg / ml, hydrochloric acid Ephedrine 11 mg / ml, levofloxacin 5 mg / ml, and the sustained-release pharmaceutical composition also includes citric acid.
[0036] The sustained-release pharmaceutical composition also includes a film matrix, and the film matrix includes film materials, plasticizers, surfactants, porogens and solvents.
[0037] The film material is povidone, methacrylate-methacrylic acid copolymer, ethylene-vinyl acetate copolymer.
[0038] Described plasticizer is propylene glycol.
[0039] The surfactant is sodium lauryl sulfate.
[0040] The porogen is polyethylene glycol.
[0041] Described solvent is ethanol, water and acetone.
[0042] The preparation method of the sustained-release pharmaceutical composition for the treatment of al...
Embodiment 3
[0046] A sustained-release pharmaceutical composition for treating allergic rhinitis, comprising the following raw materials according to mass-volume concentration: loratadine 1.2mg / ml, cromolyn disodium 23mg / ml, dexamethasone 0.25mg / ml, hydrochloric acid Ephedrine 15mg / ml, levofloxacin 7mg / ml, and the sustained-release pharmaceutical composition also includes citric acid.
[0047] The sustained-release pharmaceutical composition also includes a film matrix, and the film matrix includes film materials, plasticizers, surfactants, porogens and solvents.
[0048] The film material is ethyl cellulose.
[0049] Described plasticizer is sorbitol.
[0050] The surfactant is soybean lecithin.
[0051] The porogen is sodium chloride.
[0052] Described solvent is ethanol, water and acetone.
[0053] The preparation method of the sustained-release pharmaceutical composition for the treatment of allergic rhinitis, the steps are as follows:
[0054] 1) Weighing loratadine, disodium c...
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