Method for compounding pioglitazone hydrochloride controlled-release pellet preparation
A technology of pioglitazone hydrochloride and sustained-release pellets, which is applied in the direction of pharmaceutical formulations, drug combinations, and medical preparations containing active ingredients, etc., and can solve the problem of imperfect preparation process and equipment of double-layer osmotic pump technology and unsatisfactory drug compliance of patients To achieve the effect of small differences in individual bioavailability, reduce the number of times of taking medicine, and uniform absorption speed
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Embodiment 1
[0022] The pioglitazone hydrochloride sustained-release pellets are composed of three parts: a blank core, a drug-containing layer and a sustained-release layer; the drug-containing layer is composed of pioglitazone hydrochloride, a binder, and a solubilizer; the sustained-release layer is composed of a sustained-release material and a pore-forming agent; The composition weight percentage is: blank pellet core 70.2-83.3%, pioglitazone hydrochloride 13.0-28.6%, binder 1.2-2.0%, solubilizer 0.05-1.2%, slow-release material 3.5-13.0%, porogen 1.2-5.0% %, the sum of the above components by weight is 100%.
Embodiment 2
[0024] The composition weight percentage is: blank ball core 75.2-80.3%, pioglitazone hydrochloride 20.0-23.3%, hypromellose 1.2-2.0%, sorbitan fatty acid ester 0.07-1.2%, cellulose acetate 6.5-10.0% , povidone 2.2-4.0%, and the sum of the above components by weight is 100%.
Embodiment 3
[0026] The composition weight percentage is: blank pellet core 71.2-79.5%, pioglitazone hydrochloride 15.0-19.6%, carboxymethyl cellulose 1.2-2.0%, sodium lauryl sulfate 0.05-1.0%, ethyl cellulose aqueous dispersion product Su Lisi 3.5-11.0%, sodium chloride 1.2-3.3%, the sum of the above components by weight is 100%.
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