Method for improving stability of benserazide hydrochloride oral administration solid composition
A technology of benserazide hydrochloride and solid composition, which is applied in the field of pharmaceutical preparations, can solve the problems of solid preparation impurity detection exceeding the standard, accelerated long-term test research, and poor bioavailability, etc., to achieve shortened heating time, good protection effect, and complete granules Effect
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[0043] The benserazide hydrochloride-levodopa compound tablet was prepared by wet granulation and vacuum drying.
[0044] prescription composition Prescription mass ratio (%) Levodopa 36.4 Benserazide Hydrochloride 10.2 microcrystalline cellulose 30.8 Mannitol 1.8 Calcium hydrogen phosphate anhydrous 1.8 pregelatinized starch 5 Crospovidone 5 povidone 7 Micropowder silica gel 1 Magnesium stearate 1
[0045] Preparation:
[0046] 1) Weigh the prescription amount of levodopa, microcrystalline cellulose, 2 / 3 prescription amount of crospovidone and mix, make soft material with 5% povidone ethanol solution, granulate with 24 mesh sieve, dry in convection oven for about 2 hours.
[0047] 2) Weigh the prescription amount of benserazide hydrochloride, mannitol, anhydrous calcium hydrogen phosphate, pregelatinized starch, mix with 1 / 3 of the prescription amount of cross-linked povidone, and make soft material wi...
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