Bupropion hydrochloride sustained-release capsules and preparation method thereof
A technology of bupropion hydrochloride and sustained-release capsules, which is applied in the fields of pharmaceutical formulations, medical preparations containing active ingredients, nervous system diseases, etc., and can solve the problems of gastrointestinal motility rate, obvious individual differences, and epilepsy. To achieve the effects of reducing the incidence of adverse reactions, stabilizing changes in blood drug concentration, and improving compliance
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[0013] The preferred embodiments of the present invention are given below to describe the technical solution of the present invention in detail.
[0014] The bupropion hydrochloride sustained-release capsule of the present invention is made up of the following components, calculated by weight percentage, 62.50% bupropion hydrochloride, 6.25% tartaric acid, 9.26% sugar pills, 4.17% povidone K30 (referred to as PVPK30), 6.94% palmitic acid stearate, 0.46% acrylic resin RS100, 9.26% acrylic resin NE30D, 0.93% talc, 0.23% yellow iron oxide. Tartaric acid is a stabilizing agent to keep the stability of bupropion hydrochloride in the preparation. Povidone K30 and acrylic resin RS100 are used as adhesives. Glyceryl Palmitate Stearate is used in the barrier coating. Acrylic resin NE30D is used for sustained release coating. Talc is a lubricant. Yellow iron oxide is a coloring agent.
[0015] The preparation method of the bupropion hydrochloride sustained-release capsules of the p...
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