Medicinal preparation containing cetilistat and preparation method thereof
A pharmaceutical preparation, the technology of the new lixistat, applied in the field of medicine, can solve the problems of poor stability and slow disintegration of samples, and achieve the effects of good stability, excellent disintegration speed and excellent hardness
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Embodiment 1
[0028] Tablets containing Neolistat were prepared at the composition ratios shown in Table 1 as follows.
[0029] Briefly, Neolistat, mannitol and microcrystalline cellulose were placed in a fluid bed dry granulator, and the mixture was preheated and mixed. The mixture was granulated while spraying an aqueous solution of hydroxypropyl cellulose and yellow iron oxide to obtain a granulated powder. The obtained granulated powder was passed through a 16-mesh sieve to obtain a sieved powder. To the sieved powder was added croscarmellose sodium and magnesium stearate, and the mixture was blended in a bag to obtain a blended powder. Using a rotary tablet press, using a 14×8 mm punch, the mixed powder was tableted, each tablet 240 mg.
[0030] Table 1 prescription composition
[0031]
Embodiment 2
[0033] Tablets containing Neolistat were prepared at the composition ratios shown in Table 2 as follows.
[0034] Briefly, Neolistat, mannitol and microcrystalline cellulose were placed in a fluid bed dry granulator, and the mixture was preheated and mixed. The mixture was granulated while spraying an aqueous solution of hydroxypropyl cellulose and yellow iron oxide to obtain a granulated powder. The obtained granulated powder was passed through a 16-mesh sieve to obtain a sieved powder. To the sieved powder was added croscarmellose sodium and magnesium stearate, and the mixture was blended in a bag to obtain a blended powder. Using a rotary tablet press, using a 14×8 mm punch, the mixed powder was tableted, each tablet 300 mg.
[0035] Table 2 Prescription Composition
[0036]
Embodiment 3
[0038] Tablets containing Neolistat were prepared at the composition ratios shown in Table 3 as follows.
[0039] Preparation process: Briefly, neolistat, mannitol and microcrystalline cellulose were placed in a fluidized bed dry granulator, and the mixture was preheated and mixed. The mixture was granulated while spraying an aqueous solution of hydroxypropyl cellulose and yellow iron oxide to obtain a granulated powder. The obtained granulated powder was passed through a 16-mesh sieve to obtain a sieved powder. To the sieved powder, croscarmellose sodium and magnesium fecal acid were added, and the mixture was mixed in a bag to obtain a mixed powder. Using a rotary tablet press, using a 14×8 mm punch, the mixed powder was tableted, each tablet 360 mg.
[0040] Table 3 prescription composition
[0041]
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