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METHOD OF CIPROFLOXACIN TABLETS PREPARING

机译:环丙沙星片剂的制备方法

摘要

FIELD: medicinal industry, pharmacy. SUBSTANCE: invention relates to ready drugs. Corn starch and microcrystalline cellulose are mixed, obtained mixture is wetted with water and ciprofloxacin hydrochloride is added. Obtained mass is wetted again and subjected for wet granulation, drying, dry granulation followed by powdering with a mixture consisting of crosspovidone, aerosil, magnesium stearate, corn starch and microcrystalline cellulose and tabletting. At the first wetting water is added in the amount 10.0-12.0 wt. -% of the charge mass and at the repeated wetting, in the amount 3.0-5.0 wt. -% up to preparing the solid curdy-like mass. For preparing a mixture of powder-like components 7.0-8.5 wt.-% of corn starch and 3.6-4.4 wt.-% of microcrystalline cellulose are used and for powdering - 1.8-2.0 wt. -% and 3.1-3.5 wt.-%, respectively. Tablet strength is 5-7 kg in the process of making, decomposition time - 6-7 min. EFFECT: improved method of preparing, improved quality of tablets. 3 cl, 1 ex
机译:领域:医药工业,制药。物质:本发明涉及现成的药物。将玉米淀粉和微晶纤维素混合,将获得的混合物用水润湿,并加入盐酸环丙沙​​星。将获得的物料再次润湿并进行湿法制粒,干燥,干法制粒,然后与由交联维酮,气溶胶,硬脂酸镁,玉米淀粉和微晶纤维素组成的混合物制粉并压片。在第一次润湿时,添加的水的量为10.0-12.0重量%。 -电荷质量的-%,并且在重复润湿时,为3.0-5.0重量%。 -%直到制备固态的卷曲状物质。为了制备粉末状组分的混合物,使用7.0-8.5重量%的玉米淀粉和3.6-4.4重量%的微晶纤维素,并且用于粉化-1.8-2.0重量%。 -%和3.1-3.5重量%。片剂强度在制备过程中为5-7公斤,分解时间为6-7分钟。效果:改进了制备方法,提高了片剂质量。 3 cl,1 ex

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