Medicinal composition for treating chronic pharyngitis and preparation method and application thereof
A chronic pharyngitis and composition technology, applied in the field of pharmaceutical compositions for the treatment of chronic pharyngitis, can solve the problems of large dosage, reduce acute and chronic inflammatory reactions, promote the repair of inflammatory pathological tissues, and improve the microvascular state and hemorheology Effect
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Embodiment 1
[0026] The preparation of embodiment 1 pharmaceutical capsule of the present invention
[0027] Raw materials: 3000g of Salvia miltiorrhiza, 2000g of Scrophulariaceae, 1200g of emblica, 1000g of Coptis chinensis, appropriate amount of dextrin and magnesium stearate, making 1200 capsules in total
[0028] Preparation method:
[0029] The above 4 medicinal materials are crushed into coarse particles first, and decocted twice with 10 times the amount of water, each time for 1 hour, and the decoctions are combined, filtered, and the filtrate is concentrated to a clear paste with a relative density of 1.10 (60°C), and then added after cooling. Ethanol until the alcohol content reaches 60%, refrigerated for 24 hours, filtered, and the filtrate is decompressed to recover ethanol, dried, added dextrin and magnesium stearate, mixed evenly, packed into capsules, and obtained.
[0030] According to the theory of traditional Chinese medicine, clinical experience and pharmacological test ...
Embodiment 2
[0035] The preparation of embodiment 2 pharmaceutical composition of the present invention
[0036] Take raw materials: Scrophulariae 250g, Salvia 300g, Ophiopogon japonicus 200g, Radix Paeoniae Rubra 150g, Coptidis 150g, Burdock 150g, Emlical 150g, Campanulaceae 150g, Cicada slough 100g, Sorbic acid 1g.
[0037] The above 9 medicinal materials are first crushed into coarse particles, decocted twice with 10 times the amount of water, each time for 1 hour, the decoctions are combined, filtered, the filtrate is concentrated to a clear paste with a relative density of 1.10 (60°C), cooled and added Ethanol until the alcohol content reaches 60%, refrigerated for 24 hours, filtered, the filtrate is decompressed to recover ethanol, added sorbic acid and mixed to obtain oral liquid.
Embodiment 3 Embodiment 1
[0038] The quality control method of embodiment 3 embodiment 1 pharmaceutical composition
[0039] Determination according to high performance liquid chromatography (Appendix VID of "Chinese Pharmacopoeia" 2005 edition).
[0040] Chromatographic conditions and system suitability test use octadecylsilane bonded silica gel as filler; mobile phase is acetonitrile-water (32:68); detector is evaporative light scattering detector; Not less than 4000.
[0041] Preparation of Reference Substance Solution Accurately weigh an appropriate amount of astragaloside IV reference substance (for content determination), add methanol to make a solution containing 0.5mg per 1ml, and obtain it.
[0042] Preparation of the test solution Take 4g of the content of Example 1, accurately weighed, put in a Soxhlet extractor, add 40ml of methanol, cold soak overnight, heat and reflux for extraction for 4 hours, the extract is reclaimed and dissolved to dryness, and the residue is added with 10ml of wate...
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